7801 NP_001070868 S145C not found in SNVbox database
8834 NP_705833 Q730K not found in SNVbox database
275 NP_705833 Q967L not found in SNVbox database
1061 NP_705833 S124L not found in SNVbox database
2504 NP_705833 L354F not found in SNVbox database
3482 NP_705833 S939F not found in SNVbox database
3615 NP_705833 P455S not found in SNVbox database
3837 NP_705833 L100P not found in SNVbox database
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr1:49202064 G>C maps to NM_024603.2 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr1:49202064 G>C maps to NM_024603.2 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr1:54370405 G>A maps to NM_000792.5 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr1:54370405 G>A maps to NM_000792.5 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr1:94697029 C>T maps to NM_004815.3 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr1:94697029 C>T maps to NM_004815.3 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr1:109795730 C>T maps to NM_001408.2 H1010H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr1:109795730 C>T maps to NM_001408.2 H1010H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr1:145290476 C>G maps to ENST00000344859 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr1:145290476 C>G maps to ENST00000344859 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr1:155004225 C>T maps to NM_144622.2 W188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr1:155004225 C>T maps to NM_144622.2 W188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr1:179815799 C>T maps to NM_145034.4 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr1:179815799 C>T maps to NM_145034.4 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr10:89711892 C>T maps to NM_000314.4 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr10:89711892 C>T maps to NM_000314.4 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr11:5969346 C>T maps to NM_001003443.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr11:5969346 C>T maps to NM_001003443.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr11:31816280 G>A maps to NM_001604.4 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr11:31816280 G>A maps to NM_001604.4 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr11:51515475 C>T maps to NM_001004703.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr11:51515475 C>T maps to NM_001004703.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr11:66985218 C>T maps to NM_012308.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr11:66985218 C>T maps to NM_012308.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr11:70028646 C>T maps to NM_018043.5 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr11:70028646 C>T maps to NM_018043.5 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr12:301769 G>A maps to NM_003044.3 Y525Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr12:301769 G>A maps to NM_003044.3 Y525Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr12:102295156 T>C maps to NM_018370.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr12:102295156 T>C maps to NM_018370.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr12:110968352 A>G maps to NM_152442.3 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr12:110968352 A>G maps to NM_152442.3 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr14:21831283 G>A maps to NM_007192.3 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr14:21831283 G>A maps to NM_007192.3 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr14:23884667 G>A maps to NM_000257.2 S1735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr14:23884667 G>A maps to NM_000257.2 S1735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr14:68008607 G>A maps to NM_020715.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr14:68008607 G>A maps to NM_020715.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr14:73957814 C>T maps to NM_024644.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr14:73957814 C>T maps to NM_024644.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr17:5312066 G>A maps to NM_002532.3 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr17:5312066 G>A maps to NM_002532.3 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr17:81043035 A>G maps to NM_001004431.1 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr17:81043035 A>G maps to NM_001004431.1 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr18:59777190 G>A maps to NM_176787.4 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr18:59777190 G>A maps to NM_176787.4 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr19:6187795 C>T maps to NM_030924.3 Q623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr19:6187795 C>T maps to NM_030924.3 Q623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr19:47763904 A>T maps to NM_015603.2 K91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr19:47763904 A>T maps to NM_015603.2 K91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr19:54327176 G>A maps to ENST00000391773 D84D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr19:54327176 G>A maps to ENST00000391773 D84D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr19:56422071 G>A maps to NM_176810.2 H713H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr19:56422071 G>A maps to NM_176810.2 H713H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr2:24905932 C>G maps to NM_003743.4 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr2:24905932 C>G maps to NM_003743.4 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr2:97779625 C>G maps to NM_001164315.1 Y50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr2:97779625 C>G maps to NM_001164315.1 Y50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr2:120388229 C>A maps to NM_001029996.3 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr2:120388229 C>A maps to NM_001029996.3 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr2:141083448 T>A did not map to a codon.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr2:141083448 T>A did not map to a codon.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr2:182852606 C>G maps to ENST00000280295 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr2:182852606 C>G maps to ENST00000280295 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr2:220354644 C>T maps to NM_005876.4 L2969L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr2:220354644 C>T maps to NM_005876.4 L2969L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr2:234749403 C>T maps to NM_018410.3 R674R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr2:234749403 C>T maps to NM_018410.3 R674R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr21:46057445 T>C maps to NM_181688.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr21:46057445 T>C maps to NM_181688.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr21:47410317 C>T maps to NM_001848.2 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr21:47410317 C>T maps to NM_001848.2 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr3:123695770 T>C maps to NM_017578.2 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr3:123695770 T>C maps to NM_017578.2 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr3:125176124 C>T maps to NM_003794.2 E343E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr3:125176124 C>T maps to NM_003794.2 E343E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr4:177067238 T>C maps to NM_170710.4 H565H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr4:177067238 T>C maps to NM_170710.4 H565H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr5:32058192 A>G maps to NM_178140.2 E728E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr5:32058192 A>G maps to NM_178140.2 E728E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr5:135587502 C>T maps to NM_020389.2 W471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr5:135587502 C>T maps to NM_020389.2 W471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr6:90385184 G>A maps to NM_014611.1 L4253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr6:90385184 G>A maps to NM_014611.1 L4253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr7:4900070 G>A maps to NM_020144.4 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr7:4900070 G>A maps to NM_020144.4 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr7:39247046 C>A maps to NM_007252.3 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr7:39247046 C>A maps to NM_007252.3 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr8:77617963 T>C maps to NM_024721.4 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr8:77617963 T>C maps to NM_024721.4 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr9:77397709 C>T maps to NM_017662.4 V993V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr9:77397709 C>T maps to NM_017662.4 V993V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr9:139339533 T>C maps to NM_014866.1 L2299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr9:139339533 T>C maps to NM_014866.1 L2299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr9:139990686 A>C did not map to a codon.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr9:139990686 A>C did not map to a codon.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr9:140473184 G>A maps to NM_138778.2 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chr9:140473184 G>A maps to NM_138778.2 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chrX:34149588 A>C maps to NM_203408.3 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chrX:34149588 A>C maps to NM_203408.3 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chrX:123699279 G>T maps to NM_001163278.1 C736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4074-01A-01D-1434-08 chrX:123699279 G>T maps to NM_001163278.1 C736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:22016568 A>G maps to NM_032236.5 A969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:22016568 A>G maps to NM_032236.5 A969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:46073528 G>T maps to NM_002482.3 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:46073528 G>T maps to NM_002482.3 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:110086822 G>A maps to NM_031936.4 E393E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:110086822 G>A maps to NM_031936.4 E393E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:151146930 C>T maps to NM_013353.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:151146930 C>T maps to NM_013353.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:182026715 G>A maps to NM_001009992.1 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:182026715 G>A maps to NM_001009992.1 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:201868532 G>A maps to NM_012134.2 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:201868532 G>A maps to NM_012134.2 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:216850601 A>T maps to NM_001438.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:216850601 A>T maps to NM_001438.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:229772123 G>C maps to NM_014777.2 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr1:229772123 G>C maps to NM_014777.2 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr10:92509029 G>A maps to NM_019859.3 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr10:92509029 G>A maps to NM_019859.3 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr11:55595191 C>A maps to NM_001004739.1 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr11:55595191 C>A maps to NM_001004739.1 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr11:62445535 C>T maps to NM_015853.3 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr11:62445535 C>T maps to NM_015853.3 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr11:62520233 C>G maps to NM_024784.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr11:62520233 C>G maps to NM_024784.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr11:69462870 C>T maps to NM_053056.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr11:69462870 C>T maps to NM_053056.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr12:39947880 C>A maps to NM_005164.3 E686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr12:39947880 C>A maps to NM_005164.3 E686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr12:51404505 C>T maps to NM_001174125.1 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr12:51404505 C>T maps to NM_001174125.1 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr12:54932699 G>A maps to NM_005337.4 Q1072Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr12:54932699 G>A maps to NM_005337.4 Q1072Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr12:56566446 T>C maps to NM_003075.3 K564K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr12:56566446 T>C maps to NM_003075.3 K564K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr12:114358414 C>A did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr12:114358414 C>A did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr13:28599055 C>T maps to NM_004119.2 Q744Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr13:28599055 C>T maps to NM_004119.2 Q744Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr13:28854570 A>C maps to NM_175854.7 R738R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr13:28854570 A>C maps to NM_175854.7 R738R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr13:88327783 C>A maps to NM_015567.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr13:88327783 C>A maps to NM_015567.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr13:99042215 G>A maps to NM_005766.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr13:99042215 G>A maps to NM_005766.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr13:109817247 G>C did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr13:109817247 G>C did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr15:51696665 C>T maps to NM_181789.2 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr15:51696665 C>T maps to NM_181789.2 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr15:57925870 G>T maps to NM_001018090.3 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr15:57925870 G>T maps to NM_001018090.3 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr15:84651067 G>T maps to NM_207517.2 P896P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr15:84651067 G>T maps to NM_207517.2 P896P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr16:21014469 G>A maps to NM_017539.1 Q2028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr16:21014469 G>A maps to NM_017539.1 Q2028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr17:7577016 A>C did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr17:7577016 A>C did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr17:35913811 T>A maps to NM_007247.4 G671G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr17:35913811 T>A maps to NM_007247.4 G671G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr17:38340837 A>G maps to ENST00000456989 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr17:38340837 A>G maps to ENST00000456989 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr18:14787089 G>A maps to NM_001145029.1 W575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr18:14787089 G>A maps to NM_001145029.1 W575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr19:38960131 C>T maps to NM_000540.2 P1248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr19:38960131 C>T maps to NM_000540.2 P1248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr19:43237074 A>T maps to NM_021016.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr19:43237074 A>T maps to NM_021016.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr19:50210774 C>T maps to NM_152359.2 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr19:50210774 C>T maps to NM_152359.2 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr19:58420412 C>T maps to NM_152475.2 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr19:58420412 C>T maps to NM_152475.2 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr2:42991085 G>A maps to NM_148962.4 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr2:42991085 G>A maps to NM_148962.4 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr2:97218001 C>A maps to NM_212481.1 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr2:97218001 C>A maps to NM_212481.1 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr20:3128840 A>C maps to NM_021826.4 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr20:3128840 A>C maps to NM_021826.4 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr20:20013235 A>T maps to NM_016100.3 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr20:20013235 A>T maps to NM_016100.3 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr20:39990015 C>T maps to NM_052846.1 L731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr20:39990015 C>T maps to NM_052846.1 L731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr21:31538875 C>T maps to NM_012131.2 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr21:31538875 C>T maps to NM_012131.2 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr21:43529774 C>T maps to NM_173568.3 D541D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr21:43529774 C>T maps to NM_173568.3 D541D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr22:40660899 G>A maps to ENST00000454349 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr22:40660899 G>A maps to ENST00000454349 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr3:33427048 A>G maps to NM_012157.3 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr3:33427048 A>G maps to NM_012157.3 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr3:119458166 G>A maps to NM_033364.3 Q509Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr3:119458166 G>A maps to NM_033364.3 Q509Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr3:120365174 G>A maps to NM_000187.3 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr3:120365174 G>A maps to NM_000187.3 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr4:10083022 G>A maps to NM_017491.3 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr4:10083022 G>A maps to NM_017491.3 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr4:110890204 G>T maps to NM_001963.4 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr4:110890204 G>T maps to NM_001963.4 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr5:825359 T>C maps to NM_024786.2 K314K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr5:825359 T>C maps to NM_024786.2 K314K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr5:1246006 G>A maps to NM_182632.2 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr5:1246006 G>A maps to NM_182632.2 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr5:1321748 C>A did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr5:1321748 C>A did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr5:1488527 G>A maps to NM_024830.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr5:1488527 G>A maps to NM_024830.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr5:141358229 T>C maps to NM_183399.1 C223C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr5:141358229 T>C maps to NM_183399.1 C223C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr6:148865296 C>T maps to NM_015278.3 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr6:148865296 C>T maps to NM_015278.3 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr7:30492294 G>A maps to NM_006092.2 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr7:30492294 G>A maps to NM_006092.2 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr7:37955851 C>T maps to ENST00000223214 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr7:37955851 C>T maps to ENST00000223214 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr7:150325304 G>T maps to ENST00000438845 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr7:150325304 G>T maps to ENST00000438845 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr8:30657105 C>A maps to NM_001009552.1 G90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr8:30657105 C>A maps to NM_001009552.1 G90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr8:61778179 C>T maps to NM_017780.2 L2894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr8:61778179 C>T maps to NM_017780.2 L2894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr8:77768486 C>T maps to NM_024721.4 P3110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr8:77768486 C>T maps to NM_024721.4 P3110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr9:21971208 T>A did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr9:21971208 T>A did not map to a codon.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr9:107267226 C>A maps to NM_001004485.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr9:107267226 C>A maps to NM_001004485.1 I228I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BA-4075-01A-01D-1434-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-BA-4075-01A-01D-1434-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr9:127572375 C>T maps to NM_182487.2 I548I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr9:127572375 C>T maps to NM_182487.2 I548I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr9:136324142 G>A maps to NM_139025.3 Q1375Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr9:136324142 G>A maps to NM_139025.3 Q1375Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr9:139563026 C>T maps to NM_201446.1 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chr9:139563026 C>T maps to NM_201446.1 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chrX:54209175 C>G maps to NM_017848.4 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4075-01A-01D-1434-08 chrX:54209175 C>G maps to NM_017848.4 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:22168730 C>A did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:22168730 C>A did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:34180271 G>A maps to ENST00000373381 P1067P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:34180271 G>A maps to ENST00000373381 P1067P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:52705123 G>T maps to NM_004799.2 G679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:52705123 G>T maps to NM_004799.2 G679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:57258098 T>C maps to NM_001004303.4 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:57258098 T>C maps to NM_001004303.4 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:74507185 C>A maps to NM_001105659.1 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:74507185 C>A maps to NM_001105659.1 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:75078364 C>A maps to NM_001002912.4 G377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:75078364 C>A maps to NM_001002912.4 G377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:76365378 G>T maps to NM_002440.2 T869T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:76365378 G>T maps to NM_002440.2 T869T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:97658798 G>A maps to NM_000110.3 C816C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:97658798 G>A maps to NM_000110.3 C816C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:112028407 T>G maps to NM_020683.6 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:112028407 T>G maps to NM_020683.6 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:151001308 C>T maps to NM_021222.1 C274C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:151001308 C>T maps to NM_021222.1 C274C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:165218666 C>T maps to NM_177398.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:165218666 C>T maps to NM_177398.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:169510645 G>A maps to ENST00000367796 Q1233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:169510645 G>A maps to ENST00000367796 Q1233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:192321322 G>T maps to NM_001039152.3 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:192321322 G>T maps to NM_001039152.3 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:248551580 A>T maps to NM_001005471.1 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr1:248551580 A>T maps to NM_001005471.1 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr10:24802316 A>T maps to NM_019590.3 R711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr10:24802316 A>T maps to NM_019590.3 R711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr10:28284016 C>A maps to NM_018076.2 G19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr10:28284016 C>A maps to NM_018076.2 G19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr10:43882405 G>A maps to NM_001098204.1 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr10:43882405 G>A maps to NM_001098204.1 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr10:56106123 C>A did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr10:56106123 C>A did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr10:85992309 C>A maps to NM_015613.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr10:85992309 C>A maps to NM_015613.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr10:97918676 A>T maps to NM_014803.3 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr10:97918676 A>T maps to NM_014803.3 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr10:134885500 G>T did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr10:134885500 G>T did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:5020433 G>C maps to NM_001004755.1 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:5020433 G>C maps to NM_001004755.1 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:5799429 G>C maps to NM_001001922.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:5799429 G>C maps to NM_001001922.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:33358704 G>T maps to NM_005734.3 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:33358704 G>T maps to NM_005734.3 E436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:49974252 T>C maps to NM_001001955.2 N93N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:49974252 T>C maps to NM_001001955.2 N93N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:55110930 T>A maps to NM_001005274.1 C85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:55110930 T>A maps to NM_001005274.1 C85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:55606808 T>A maps to NM_001005496.1 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:55606808 T>A maps to NM_001005496.1 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:55927514 G>C maps to NM_001004058.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:55927514 G>C maps to NM_001004058.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:57118348 C>T maps to NM_002559.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:57118348 C>T maps to NM_002559.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:57379318 G>T maps to ENST00000403558 E430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:57379318 G>T maps to ENST00000403558 E430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:60906238 C>A maps to NM_017966.4 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:60906238 C>A maps to NM_017966.4 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:62398538 G>A maps to NM_198335.2 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:62398538 G>A maps to NM_198335.2 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:63967639 G>T did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:63967639 G>T did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:67049152 G>T maps to NM_001619.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:67049152 G>T maps to NM_001619.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:70333069 C>A maps to ENST00000338508 E1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:70333069 C>A maps to ENST00000338508 E1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:70333673 G>A maps to ENST00000338508 C902C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:70333673 G>A maps to ENST00000338508 C902C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:89892473 G>T maps to NM_005467.3 G320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr11:89892473 G>T maps to NM_005467.3 G320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr12:49433006 G>A maps to NM_003482.3 S2788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr12:49433006 G>A maps to NM_003482.3 S2788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr12:72090219 A>G maps to NM_018279.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr12:72090219 A>G maps to NM_018279.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr12:109872839 A>G did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr12:109872839 A>G did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr13:28011270 G>A maps to NM_152912.4 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr13:28011270 G>A maps to NM_152912.4 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr14:23886824 G>A maps to NM_000257.2 L1414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr14:23886824 G>A maps to NM_000257.2 L1414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr14:75230941 G>T maps to NM_019589.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr14:75230941 G>T maps to NM_019589.2 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr14:88434806 T>C maps to NM_000153.2 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr14:88434806 T>C maps to NM_000153.2 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr14:94394801 G>T maps to NM_138344.3 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr14:94394801 G>T maps to NM_138344.3 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr15:22382663 C>A maps to NM_001005241.1 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr15:22382663 C>A maps to NM_001005241.1 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr15:22382711 G>A maps to NM_001005241.1 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr15:22382711 G>A maps to NM_001005241.1 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr15:48752446 G>A maps to NM_000138.4 P1764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr15:48752446 G>A maps to NM_000138.4 P1764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr15:69335138 G>T maps to NM_024505.3 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr15:69335138 G>T maps to NM_024505.3 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr16:3778855 G>A maps to NM_004380.2 P2064P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr16:3778855 G>A maps to NM_004380.2 P2064P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr16:4855257 C>A maps to NM_032569.3 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr16:4855257 C>A maps to NM_032569.3 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr16:20787220 C>A maps to NM_005622.3 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr16:20787220 C>A maps to NM_005622.3 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr16:75269449 C>A maps to NM_001170714.1 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr16:75269449 C>A maps to NM_001170714.1 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr16:81094969 C>T maps to NM_152337.2 Q328Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr16:81094969 C>T maps to NM_152337.2 Q328Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr17:2238188 T>A maps to NM_018128.4 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr17:2238188 T>A maps to NM_018128.4 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr17:8732224 G>T maps to NM_001010855.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr17:8732224 G>T maps to NM_001010855.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr17:21204271 C>G maps to NM_145109.2 Y122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr17:21204271 C>G maps to NM_145109.2 Y122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr18:2751279 T>C maps to NM_015295.2 F1390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr18:2751279 T>C maps to NM_015295.2 F1390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr18:9563519 T>A maps to NM_001042388.1 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr18:9563519 T>A maps to NM_001042388.1 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr18:40850485 G>T maps to NM_020783.3 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr18:40850485 G>T maps to NM_020783.3 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr19:15807870 G>A maps to NM_023944.2 E517E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr19:15807870 G>A maps to NM_023944.2 E517E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr19:18545773 G>A maps to NM_016368.4 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr19:18545773 G>A maps to NM_016368.4 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr19:54868567 C>T maps to NM_002287.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr19:54868567 C>T maps to NM_002287.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr19:55106643 C>A maps to NM_006863.1 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr19:55106643 C>A maps to NM_006863.1 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr19:57647165 G>C maps to NM_052882.1 S180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr19:57647165 G>C maps to NM_052882.1 S180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:116510866 T>C maps to NM_020868.3 C356C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:116510866 T>C maps to NM_020868.3 C356C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:163133238 C>G maps to NM_022168.2 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:163133238 C>G maps to NM_022168.2 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:179537202 C>A maps to NM_133378.4 E10320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:179537202 C>A maps to NM_133378.4 E10320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:179553840 G>C maps to NM_133378.4 P9434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:179553840 G>C maps to NM_133378.4 P9434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:196723251 A>T maps to NM_018897.2 G2671G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:196723251 A>T maps to NM_018897.2 G2671G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:230652325 T>C maps to ENST00000389044 A1603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:230652325 T>C maps to ENST00000389044 A1603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr20:33867550 C>T did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr20:33867550 C>T did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr20:62493606 C>G maps to NM_080622.3 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr20:62493606 C>G maps to NM_080622.3 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr21:34011283 T>A maps to NM_003895.3 P1322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr21:34011283 T>A maps to NM_003895.3 P1322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr21:47821490 G>A maps to NM_006031.5 Q1606Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr21:47821490 G>A maps to NM_006031.5 Q1606Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr22:26423400 G>C maps to ENST00000407587 G2489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr22:26423400 G>C maps to ENST00000407587 G2489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:46062614 G>A maps to NM_005283.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:46062614 G>A maps to NM_005283.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:49227303 G>T did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:49227303 G>T did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:69168974 T>C maps to NM_198271.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:69168974 T>C maps to NM_198271.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:93615488 A>T maps to NM_000313.3 L299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:93615488 A>T maps to NM_000313.3 L299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:100962534 C>A maps to NM_016247.2 V880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:100962534 C>A maps to NM_016247.2 V880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:120489716 G>T maps to NM_005513.2 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:120489716 G>T maps to NM_005513.2 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:128712027 C>T maps to NM_020741.2 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:128712027 C>T maps to NM_020741.2 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:132408076 C>T maps to ENST00000393156 W908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:132408076 C>T maps to ENST00000393156 W908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:138763108 C>T maps to NM_001134657.1 W118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:138763108 C>T maps to NM_001134657.1 W118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:154138917 T>C maps to NM_001038705.1 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:154138917 T>C maps to NM_001038705.1 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:164737395 G>T maps to NM_001041.3 P1139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:164737395 G>T maps to NM_001041.3 P1139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:179095130 G>A did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr3:179095130 G>A did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr4:44688652 A>G maps to NM_021927.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr4:44688652 A>G maps to NM_021927.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr4:83375979 G>A maps to NM_021204.3 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr4:83375979 G>A maps to NM_021204.3 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr4:107845852 G>A maps to NM_014421.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr4:107845852 G>A maps to NM_014421.2 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr4:111431454 G>T maps to NM_001977.3 G417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr4:111431454 G>T maps to NM_001977.3 G417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr4:120221510 G>C maps to NM_001170330.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr4:120221510 G>C maps to NM_001170330.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr4:173150915 G>T did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr4:173150915 G>T did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr5:13735960 G>A maps to NM_001369.2 Q3846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr5:13735960 G>A maps to NM_001369.2 Q3846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr5:24537585 C>T maps to NM_006727.3 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr5:24537585 C>T maps to NM_006727.3 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr5:26885966 T>C maps to NM_016279.3 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr5:26885966 T>C maps to NM_016279.3 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr5:39153578 G>C maps to ENST00000263405 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr5:39153578 G>C maps to ENST00000263405 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr5:45396680 G>T maps to NM_021072.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr5:45396680 G>T maps to NM_021072.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr5:58147123 G>A maps to NM_138453.2 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr5:58147123 G>A maps to NM_138453.2 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr5:140209241 G>T maps to NM_018909.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr5:140209241 G>T maps to NM_018909.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr6:41162311 G>A maps to ENST00000373108 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr6:41162311 G>A maps to ENST00000373108 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr6:51947242 G>A maps to NM_138694.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr6:51947242 G>A maps to NM_138694.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr6:57472414 A>T maps to NM_000947.2 K402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr6:57472414 A>T maps to NM_000947.2 K402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr6:149997416 T>A maps to NM_004690.2 T954T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr6:149997416 T>A maps to NM_004690.2 T954T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr6:168464321 G>T maps to NM_024919.3 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr6:168464321 G>T maps to NM_024919.3 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr7:37355564 C>T did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr7:37355564 C>T did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr7:37960495 C>A maps to NM_017549.3 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr7:37960495 C>A maps to NM_017549.3 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr7:92902041 A>G maps to NM_017667.2 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr7:92902041 A>G maps to NM_017667.2 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr7:143633044 G>T maps to NM_001004685.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr7:143633044 G>T maps to NM_001004685.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr8:54163408 C>G maps to NM_000912.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr8:54163408 C>G maps to NM_000912.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr8:100146858 G>T did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr8:100146858 G>T did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr9:104319793 G>A maps to NM_019592.5 E766E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr9:104319793 G>A maps to NM_019592.5 E766E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr9:125273991 C>A maps to NM_054107.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr9:125273991 C>A maps to NM_054107.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr9:125486582 C>T maps to NM_001005235.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr9:125486582 C>T maps to NM_001005235.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chrX:1748782 G>A maps to NM_001171038.1 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chrX:1748782 G>A maps to NM_001171038.1 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chrX:101970807 G>A maps to NM_138437.5 Q337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chrX:101970807 G>A maps to NM_138437.5 Q337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:26648787 C>G maps to NM_001039775.3 V1588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:26648787 C>G maps to NM_001039775.3 V1588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:27190330 G>T maps to NM_006142.3 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:27190330 G>T maps to NM_006142.3 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:40422866 C>T maps to NM_001136493.1 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:40422866 C>T maps to NM_001136493.1 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:44820584 C>G maps to NM_024066.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:44820584 C>G maps to NM_024066.1 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:54332511 T>C maps to NM_018982.4 K189K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:54332511 T>C maps to NM_018982.4 K189K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:67889985 G>A maps to NM_001018067.1 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:67889985 G>A maps to NM_001018067.1 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:111989743 G>A maps to NM_024102.2 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:111989743 G>A maps to NM_024102.2 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:113212163 G>T did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:113212163 G>T did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:155039241 C>G maps to NM_182689.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:155039241 C>G maps to NM_182689.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:169672450 C>T maps to NM_000655.4 K312K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:169672450 C>T maps to NM_000655.4 K312K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:183511285 C>T maps to ENST00000367537 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:183511285 C>T maps to ENST00000367537 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:215848780 G>A maps to ENST00000366943 Q4158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr1:215848780 G>A maps to ENST00000366943 Q4158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr10:27700798 C>T maps to NM_001034842.3 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr10:27700798 C>T maps to NM_001034842.3 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr10:70775626 G>T maps to NM_015634.3 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr10:70775626 G>T maps to NM_015634.3 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr10:105006202 G>A maps to NM_001143909.1 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr10:105006202 G>A maps to NM_001143909.1 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr11:5020493 C>T maps to NM_001004755.1 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr11:5020493 C>T maps to NM_001004755.1 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr11:19077742 G>T maps to NM_054030.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr11:19077742 G>T maps to NM_054030.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr11:70170533 C>T maps to NM_003626.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr11:70170533 C>T maps to NM_003626.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr11:85979510 C>T maps to ENST00000351625 Q292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr11:85979510 C>T maps to ENST00000351625 Q292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr11:119103213 C>T maps to NM_005188.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr11:119103213 C>T maps to NM_005188.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr11:120998983 G>A maps to NM_005422.2 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr11:120998983 G>A maps to NM_005422.2 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:351876 G>C maps to NM_016615.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:351876 G>C maps to NM_016615.3 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:49075373 C>A maps to NM_017822.3 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:49075373 C>A maps to NM_017822.3 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:70004348 C>A maps to NM_201550.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:70004348 C>A maps to NM_201550.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:102492897 G>A maps to NM_024057.2 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:102492897 G>A maps to NM_024057.2 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:111078306 G>C maps to NM_001082538.2 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:111078306 G>C maps to NM_001082538.2 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:111336786 C>T maps to NM_152591.1 Y400Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:111336786 C>T maps to NM_152591.1 Y400Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:120530922 C>T maps to NM_207311.2 I560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:120530922 C>T maps to NM_207311.2 I560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:123950296 C>G maps to NM_180699.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr12:123950296 C>G maps to NM_180699.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr14:20295738 C>T maps to NM_001004723.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr14:20295738 C>T maps to NM_001004723.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr14:69256567 G>A maps to NM_004926.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr14:69256567 G>A maps to NM_004926.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr14:71485845 C>T maps to NM_014982.2 L1039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr14:71485845 C>T maps to NM_014982.2 L1039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr14:96730570 G>C maps to NM_000710.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr14:96730570 G>C maps to NM_000710.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr15:49176471 G>T maps to NM_203349.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr15:49176471 G>T maps to NM_203349.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr15:66791762 C>T maps to NM_000968.2 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr15:66791762 C>T maps to NM_000968.2 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr15:73862515 C>T maps to NM_012428.3 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr15:73862515 C>T maps to NM_012428.3 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr16:823206 G>T maps to NM_001025190.1 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr16:823206 G>T maps to NM_001025190.1 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr16:29884919 G>A maps to NM_201575.2 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr16:29884919 G>A maps to NM_201575.2 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:4542785 G>A maps to NM_001140.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:4542785 G>A maps to NM_001140.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:4863613 C>A did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:4863613 C>A did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:33348691 G>A maps to NM_001017368.1 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:33348691 G>A maps to NM_001017368.1 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:33469077 G>A maps to NM_018096.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:33469077 G>A maps to NM_018096.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:39847032 G>A did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:39847032 G>A did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:41622707 C>A maps to NM_001079675.1 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:41622707 C>A maps to NM_001079675.1 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:59968948 C>T maps to NM_020748.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:59968948 C>T maps to NM_020748.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:60758227 G>A maps to NM_006039.3 A847A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:60758227 G>A maps to NM_006039.3 A847A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:73658603 C>T maps to NM_004259.5 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr17:73658603 C>T maps to NM_004259.5 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr18:12264383 G>T maps to ENST00000342845 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr18:12264383 G>T maps to ENST00000342845 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:3148634 C>T maps to NM_002068.2 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:3148634 C>T maps to NM_002068.2 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:5914739 C>A maps to ENST00000394521 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:5914739 C>A maps to ENST00000394521 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:9452471 A>G maps to NM_032497.1 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:9452471 A>G maps to NM_032497.1 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:10395131 G>T maps to NM_000201.2 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:10395131 G>T maps to NM_000201.2 E327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:17476502 G>C maps to NM_031310.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:17476502 G>C maps to NM_031310.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:19656360 C>A maps to NM_153221.2 R1003R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:19656360 C>A maps to NM_153221.2 R1003R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:33183420 C>G maps to NM_001105570.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:33183420 C>G maps to NM_001105570.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:35941407 C>G maps to NM_005306.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:35941407 C>G maps to NM_005306.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:36278703 C>T maps to ENST00000007510 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:36278703 C>T maps to ENST00000007510 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:40357469 G>C maps to NM_003890.2 V5281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:40357469 G>C maps to NM_003890.2 V5281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:57175753 G>A maps to NM_001005850.1 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:57175753 G>A maps to NM_001005850.1 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:58101556 T>G maps to NM_001010879.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr19:58101556 T>G maps to NM_001010879.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr2:85598301 G>T maps to NM_001135023.1 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr2:85598301 G>T maps to NM_001135023.1 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr2:120369264 C>T maps to NM_001029996.3 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr2:120369264 C>T maps to NM_001029996.3 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr2:211521292 C>A maps to NM_001122633.1 V1207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr2:211521292 C>A maps to NM_001122633.1 V1207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr2:219510997 C>T maps to NM_001105537.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr2:219510997 C>T maps to NM_001105537.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr2:238255175 C>T maps to NM_004369.3 Q2354Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr2:238255175 C>T maps to NM_004369.3 Q2354Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr20:32026797 G>A maps to NM_003098.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr20:32026797 G>A maps to NM_003098.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr20:33730262 C>A maps to NM_018217.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr20:33730262 C>A maps to NM_018217.2 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr20:35299788 C>G maps to ENST00000373803 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr20:35299788 C>G maps to ENST00000373803 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr20:37356987 G>A maps to NM_080552.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr20:37356987 G>A maps to NM_080552.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr21:10959801 T>C did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr21:10959801 T>C did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr21:39671930 C>T maps to NM_170736.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr21:39671930 C>T maps to NM_170736.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr21:47422130 G>C did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr21:47422130 G>C did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr22:24580745 C>G maps to NM_019601.3 S207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr22:24580745 C>G maps to NM_019601.3 S207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr22:30689979 G>A maps to ENST00000403477 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr22:30689979 G>A maps to ENST00000403477 F282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:13538258 C>T maps to NM_024827.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:13538258 C>T maps to NM_024827.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:25670594 G>A maps to ENST00000264331 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:25670594 G>A maps to ENST00000264331 F577F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:57291321 A>G maps to NM_012096.2 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:57291321 A>G maps to NM_012096.2 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:107492190 G>A maps to NM_001142568.1 E541E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:107492190 G>A maps to NM_001142568.1 E541E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:114069346 G>A maps to NM_001164342.1 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:114069346 G>A maps to NM_001164342.1 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:130361867 G>A did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:130361867 G>A did not map to a codon.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:171431714 C>G maps to NM_002662.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:171431714 C>G maps to NM_002662.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:187447043 G>A maps to NM_001706.4 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:187447043 G>A maps to NM_001706.4 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:195782121 C>G maps to NM_001128148.1 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr3:195782121 C>G maps to NM_001128148.1 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr4:164271638 C>T maps to NM_006174.2 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr4:164271638 C>T maps to NM_006174.2 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr5:13864528 G>A maps to NM_001369.2 L1525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr5:13864528 G>A maps to NM_001369.2 L1525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr5:56531815 G>A maps to NM_001127236.2 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr5:56531815 G>A maps to NM_001127236.2 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr5:63256427 G>A maps to NM_000524.2 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr5:63256427 G>A maps to NM_000524.2 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr5:65008793 G>A maps to NM_019072.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr5:65008793 G>A maps to NM_019072.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr5:140230179 G>A maps to NM_031857.1 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr5:140230179 G>A maps to NM_031857.1 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr5:140502347 A>G maps to NM_018938.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr5:140502347 A>G maps to NM_018938.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr5:140868962 G>C maps to NM_018929.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr5:140868962 G>C maps to NM_018929.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:27834626 C>T maps to NM_005322.2 *227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:27834626 C>T maps to NM_005322.2 *227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:31597335 G>A maps to NM_080686.2 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:31597335 G>A maps to NM_080686.2 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:33165571 G>A maps to ENST00000374685 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:33165571 G>A maps to ENST00000374685 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:56458613 C>T maps to ENST00000361203 L3980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:56458613 C>T maps to ENST00000361203 L3980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:74229716 G>A maps to NM_001402.5 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:74229716 G>A maps to NM_001402.5 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:89974232 G>C maps to NM_002043.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:89974232 G>C maps to NM_002043.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:136888995 G>A maps to NM_005923.3 F1178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:136888995 G>A maps to NM_005923.3 F1178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:168276154 C>G maps to ENST00000400822 S239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr6:168276154 C>G maps to ENST00000400822 S239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr7:6193668 G>C maps to ENST00000404835 A828A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr7:6193668 G>C maps to ENST00000404835 A828A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr7:100678728 C>G maps to NM_001040105.1 V1344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr7:100678728 C>G maps to NM_001040105.1 V1344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr7:117060269 C>T maps to NM_130768.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr7:117060269 C>T maps to NM_130768.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr7:117232002 G>A maps to NM_000492.3 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr7:117232002 G>A maps to NM_000492.3 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr7:138969090 C>G maps to NM_173569.3 S1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr7:138969090 C>G maps to NM_173569.3 S1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr7:151684343 G>C maps to NM_145292.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr7:151684343 G>C maps to NM_145292.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr8:12878577 C>T maps to NM_020844.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr8:12878577 C>T maps to NM_020844.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr8:68419034 C>T maps to NM_020361.4 W208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr8:68419034 C>T maps to NM_020361.4 W208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr8:81905366 G>A maps to NM_018440.3 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr8:81905366 G>A maps to NM_018440.3 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr9:5029861 C>T maps to NM_004972.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr9:5029861 C>T maps to NM_004972.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr9:37503069 G>A maps to NM_022490.1 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr9:37503069 G>A maps to NM_022490.1 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr9:84606905 C>G maps to NM_001001670.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr9:84606905 C>G maps to NM_001001670.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr9:91617110 C>T maps to NM_005226.2 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr9:91617110 C>T maps to NM_005226.2 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr9:100862395 G>C maps to NM_033219.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr9:100862395 G>C maps to NM_033219.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr9:120476115 T>C maps to NM_138554.3 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chr9:120476115 T>C maps to NM_138554.3 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chrX:16142342 C>T maps to NM_005314.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chrX:16142342 C>T maps to NM_005314.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chrX:30269380 C>A maps to NM_177404.2 Y257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chrX:30269380 C>A maps to NM_177404.2 Y257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chrX:46466623 C>A maps to NM_032591.1 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chrX:46466623 C>A maps to NM_032591.1 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chrX:50089688 C>T maps to NM_033031.2 I1231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chrX:50089688 C>T maps to NM_033031.2 I1231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chrX:54112313 C>T maps to NM_017848.4 Q891Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chrX:54112313 C>T maps to NM_017848.4 Q891Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chrX:101911991 C>T maps to NM_001184727.1 Q1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chrX:101911991 C>T maps to NM_001184727.1 Q1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chrX:105149321 C>G maps to NM_198465.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chrX:105149321 C>G maps to NM_198465.2 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chrX:153689683 C>T maps to NM_017514.3 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4077-01B-01D-1434-08 chrX:153689683 C>T maps to NM_017514.3 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:33237515 G>A maps to NM_020888.2 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:33237515 G>A maps to NM_020888.2 L912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:45472641 T>A maps to NM_024602.5 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:45472641 T>A maps to NM_024602.5 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:47609431 A>C did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:47609431 A>C did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:103548501 G>A maps to NM_080629.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:103548501 G>A maps to NM_080629.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:152280765 G>T maps to NM_002016.1 S2199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:152280765 G>T maps to NM_002016.1 S2199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:158389858 G>A maps to NM_001004476.1 Y266Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:158389858 G>A maps to NM_001004476.1 Y266Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:161018683 A>G maps to NM_001025598.1 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:161018683 A>G maps to NM_001025598.1 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:167024301 A>T maps to NM_005814.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:167024301 A>T maps to NM_005814.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:167408591 G>A maps to NM_198053.2 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:167408591 G>A maps to NM_198053.2 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:216850745 G>A maps to NM_001438.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:216850745 G>A maps to NM_001438.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:223568028 C>G maps to NM_152610.2 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:223568028 C>G maps to NM_152610.2 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:226549217 C>T maps to NM_001618.3 Q996Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:226549217 C>T maps to NM_001618.3 Q996Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:230827171 G>A maps to NM_007357.2 K659K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:230827171 G>A maps to NM_007357.2 K659K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:237670114 G>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:237670114 G>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:241761197 C>T maps to NM_014322.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr1:241761197 C>T maps to NM_014322.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:26512887 C>A maps to NM_001134366.1 S198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:26512887 C>A maps to NM_001134366.1 S198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:48388396 G>T maps to NM_002900.2 P827P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:48388396 G>T maps to NM_002900.2 P827P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:50532656 G>A maps to NM_001135196.1 Q689Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:50532656 G>A maps to NM_001135196.1 Q689Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:52573751 G>T maps to NM_138932.2 Y404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:52573751 G>T maps to NM_138932.2 Y404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:101591438 G>A maps to NM_000392.3 A985A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:101591438 G>A maps to NM_000392.3 A985A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:103558943 A>C maps to NM_012215.3 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:103558943 A>C maps to NM_012215.3 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:104161252 C>A maps to NM_001077494.1 P757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:104161252 C>A maps to NM_001077494.1 P757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:108427559 G>T maps to NM_001013031.1 C730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:108427559 G>T maps to NM_001013031.1 C730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:114910774 C>T maps to NM_030756.4 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:114910774 C>T maps to NM_030756.4 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:117045742 G>T maps to NM_207303.2 G751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:117045742 G>T maps to NM_207303.2 G751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:128974407 G>T maps to NM_001039762.2 Y84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:128974407 G>T maps to NM_001039762.2 Y84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:135438989 C>T maps to ENST00000443774 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr10:135438989 C>T maps to ENST00000443774 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:5602861 C>A maps to NM_001005162.2 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:5602861 C>A maps to NM_001005162.2 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:34219029 C>T maps to NM_145804.2 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:34219029 C>T maps to NM_145804.2 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:40136240 C>A maps to NM_020929.1 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:40136240 C>A maps to NM_020929.1 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:45970964 G>A maps to ENST00000257821 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:45970964 G>A maps to ENST00000257821 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:55944603 C>T maps to NM_001005492.1 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:55944603 C>T maps to NM_001005492.1 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:56258411 C>A maps to NM_001005282.1 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:56258411 C>A maps to NM_001005282.1 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:59132215 T>C maps to NM_001004729.1 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:59132215 T>C maps to NM_001004729.1 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:60718767 G>A maps to NM_016582.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:60718767 G>A maps to NM_016582.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:62533148 G>T maps to NM_002696.2 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:62533148 G>T maps to NM_002696.2 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:65546370 C>G maps to NM_138368.3 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:65546370 C>G maps to NM_138368.3 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:88781021 G>A maps to NM_001143831.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:88781021 G>A maps to NM_001143831.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:108213983 A>G maps to NM_000051.3 E2768E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:108213983 A>G maps to NM_000051.3 E2768E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:111896159 C>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:111896159 C>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:2929960 G>A maps to NM_018463.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:2929960 G>A maps to NM_018463.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:6958257 T>C maps to NM_031299.4 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:6958257 T>C maps to NM_031299.4 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:8630045 A>T maps to NM_001007033.1 K206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:8630045 A>T maps to NM_001007033.1 K206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:9262517 C>T maps to NM_000014.4 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:9262517 C>T maps to NM_000014.4 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:18644452 T>G maps to NM_004570.4 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:18644452 T>G maps to NM_004570.4 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:41422959 T>A maps to NM_001843.2 V973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:41422959 T>A maps to NM_001843.2 V973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:101603500 G>A maps to NM_145913.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:101603500 G>A maps to NM_145913.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:106760310 A>G maps to NM_018082.5 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:106760310 A>G maps to NM_018082.5 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:124221736 G>T maps to NM_012463.3 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr12:124221736 G>T maps to NM_012463.3 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr13:20039643 A>T maps to NM_199254.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr13:20039643 A>T maps to NM_199254.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr13:46357978 C>A maps to NM_198849.2 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr13:46357978 C>A maps to NM_198849.2 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr14:20403894 C>T maps to NM_001004063.2 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr14:20403894 C>T maps to NM_001004063.2 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr14:20666108 C>A maps to NM_001005503.1 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr14:20666108 C>A maps to NM_001005503.1 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr14:50912807 G>A maps to NM_198794.1 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr14:50912807 G>A maps to NM_198794.1 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr14:88411944 C>T maps to NM_000153.2 W541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr14:88411944 C>T maps to NM_000153.2 W541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr15:24922339 T>G maps to NM_018958.2 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr15:24922339 T>G maps to NM_018958.2 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr15:45460273 C>G maps to ENST00000437903 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr15:45460273 C>G maps to ENST00000437903 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr15:48428996 C>A maps to NM_205850.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr15:48428996 C>A maps to NM_205850.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr15:50929754 C>A maps to NM_017672.4 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr15:50929754 C>A maps to NM_017672.4 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr15:54307584 T>C maps to ENST00000260323 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr15:54307584 T>C maps to ENST00000260323 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr15:62312737 C>A did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr15:62312737 C>A did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr15:65994822 T>G maps to ENST00000443035 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr15:65994822 T>G maps to ENST00000443035 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr16:26147208 G>T maps to NM_006040.2 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr16:26147208 G>T maps to NM_006040.2 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr16:67168321 C>T maps to NM_025187.3 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr16:67168321 C>T maps to NM_025187.3 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr16:67862384 C>T maps to NM_025082.3 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr16:67862384 C>T maps to NM_025082.3 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr16:68056394 C>A maps to NM_018380.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr16:68056394 C>A maps to NM_018380.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr16:70989377 C>A maps to NM_032821.2 L2071L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr16:70989377 C>A maps to NM_032821.2 L2071L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr16:74519692 C>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr16:74519692 C>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:7577609 T>C did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:7577609 T>C did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:10408505 C>A maps to NM_005963.3 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:10408505 C>A maps to NM_005963.3 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:11607760 T>C did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:11607760 T>C did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:41738515 G>A maps to NM_004527.3 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:41738515 G>A maps to NM_004527.3 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:42476284 T>A maps to NM_001002909.2 R1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:42476284 T>A maps to NM_001002909.2 R1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:60755932 G>T maps to NM_006039.3 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:60755932 G>T maps to NM_006039.3 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:62291205 T>C maps to NM_018469.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:62291205 T>C maps to NM_018469.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:73871027 C>A maps to NM_033452.2 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr17:73871027 C>A maps to NM_033452.2 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr18:7016586 C>A maps to NM_005559.2 T964T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr18:7016586 C>A maps to NM_005559.2 T964T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr18:47108774 C>T maps to NM_006033.2 N360N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr18:47108774 C>T maps to NM_006033.2 N360N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:3664870 C>T maps to NM_012398.2 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:3664870 C>T maps to NM_012398.2 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:4200160 C>T maps to ENST00000262970 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:4200160 C>T maps to ENST00000262970 D202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:9007502 G>T maps to NM_024690.2 P13155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:9007502 G>T maps to NM_024690.2 P13155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:10794208 T>C maps to NM_017620.2 F618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:10794208 T>C maps to NM_017620.2 F618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:11510942 T>C maps to NM_001161616.1 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:11510942 T>C maps to NM_001161616.1 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:21607278 T>C maps to NM_001076678.2 C606C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:21607278 T>C maps to NM_001076678.2 C606C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:33482783 A>T maps to NM_033103.4 L530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:33482783 A>T maps to NM_033103.4 L530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:33696632 C>T maps to NM_002333.3 D319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:33696632 C>T maps to NM_002333.3 D319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:36341872 G>A maps to NM_004646.3 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:36341872 G>A maps to NM_004646.3 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:36964330 T>C maps to NM_001145343.1 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:36964330 T>C maps to NM_001145343.1 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:42352589 C>A maps to ENST00000427618 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:42352589 C>A maps to ENST00000427618 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:54314438 G>T maps to ENST00000391773 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr19:54314438 G>T maps to ENST00000391773 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:56602976 T>A maps to NM_001080433.1 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:56602976 T>A maps to NM_001080433.1 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:80136776 G>T maps to ENST00000402739 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:80136776 G>T maps to ENST00000402739 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:107042507 G>T maps to ENST00000304514 S881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:107042507 G>T maps to ENST00000304514 S881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:170062966 G>A maps to NM_004525.2 V2421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:170062966 G>A maps to NM_004525.2 V2421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:179583154 G>T maps to NM_133378.4 T6982T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:179583154 G>T maps to NM_133378.4 T6982T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:191064815 G>A maps to NM_032321.2 W77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:191064815 G>A maps to NM_032321.2 W77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:224765919 C>T maps to NM_020830.3 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:224765919 C>T maps to NM_020830.3 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:233198641 G>A maps to NM_152383.4 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr2:233198641 G>A maps to NM_152383.4 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr20:21376611 C>T maps to NM_033176.1 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr20:21376611 C>T maps to NM_033176.1 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr20:23966369 C>T maps to NM_178311.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr20:23966369 C>T maps to NM_178311.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr20:37395020 G>A did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr20:37395020 G>A did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr20:61833965 C>A maps to NM_017798.3 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr20:61833965 C>A maps to NM_017798.3 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr22:36541543 G>A maps to NM_145640.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr22:36541543 G>A maps to NM_145640.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:3886402 C>A maps to NM_020873.5 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:3886402 C>A maps to NM_020873.5 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:49161039 C>T maps to NM_002292.3 E1274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:49161039 C>T maps to NM_002292.3 E1274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:50421636 G>A maps to ENST00000435965 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:50421636 G>A maps to ENST00000435965 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:89521721 G>T maps to NM_005233.5 T933T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:89521721 G>T maps to NM_005233.5 T933T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:96706793 C>T maps to NM_001080448.2 C357C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:96706793 C>T maps to NM_001080448.2 C357C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:108159996 C>T maps to NM_014981.1 E942E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:108159996 C>T maps to NM_014981.1 E942E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:146309587 G>T maps to NM_001085420.1 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:146309587 G>T maps to NM_001085420.1 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:154146444 G>T maps to NM_001038705.1 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:154146444 G>T maps to NM_001038705.1 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:167437848 C>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:167437848 C>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:179472518 G>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:179472518 G>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:194063362 G>T maps to NM_001080513.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:194063362 G>T maps to NM_001080513.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:196098826 G>A maps to NM_015562.1 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr3:196098826 G>A maps to NM_015562.1 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr4:46252333 G>A maps to ENST00000507069 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr4:46252333 G>A maps to ENST00000507069 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr4:156632327 G>T maps to NM_001130684.1 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr4:156632327 G>T maps to NM_001130684.1 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr4:158262466 C>T maps to NM_000826.3 I632I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr4:158262466 C>T maps to NM_000826.3 I632I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr4:175896742 G>T maps to NM_014269.4 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr4:175896742 G>T maps to NM_014269.4 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr5:9052124 C>T maps to NM_003966.2 W902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr5:9052124 C>T maps to NM_003966.2 W902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr5:13894842 C>A maps to NM_001369.2 E783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr5:13894842 C>A maps to NM_001369.2 E783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr5:31983278 C>T maps to NM_178140.2 C165C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr5:31983278 C>T maps to NM_178140.2 C165C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr5:33588884 G>T maps to NM_030955.2 S895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr5:33588884 G>T maps to NM_030955.2 S895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr5:150924597 C>T maps to NM_001447.2 R2030R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr5:150924597 C>T maps to NM_001447.2 R2030R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr5:159680600 G>A maps to NM_024565.5 H364H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr5:159680600 G>A maps to NM_024565.5 H364H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:33283757 C>A maps to NM_001145338.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:33283757 C>A maps to NM_001145338.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:38840415 C>T maps to ENST00000327475 C2353C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:38840415 C>T maps to ENST00000327475 C2353C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:39272354 G>C maps to NM_031460.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:39272354 G>C maps to NM_031460.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:42637958 G>T maps to NM_015255.2 A1337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:42637958 G>T maps to NM_015255.2 A1337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:51890863 C>T maps to NM_138694.3 W1248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:51890863 C>T maps to NM_138694.3 W1248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:55441887 A>C maps to NM_019036.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:55441887 A>C maps to NM_019036.2 A62A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BA-4078-01A-01D-1434-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-BA-4078-01A-01D-1434-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:90604607 C>T maps to NM_032602.1 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:90604607 C>T maps to NM_032602.1 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:110714169 C>T maps to NM_003649.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:110714169 C>T maps to NM_003649.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:112443311 G>A maps to NM_001105206.1 S1460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:112443311 G>A maps to NM_001105206.1 S1460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:139576739 C>T maps to ENST00000358430 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:139576739 C>T maps to ENST00000358430 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:144843113 A>G did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr6:144843113 A>G did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:71571223 C>T maps to NM_031468.3 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:71571223 C>T maps to NM_031468.3 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:94879403 G>T maps to NM_001166160.1 E745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:94879403 G>T maps to NM_001166160.1 E745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:95034734 C>T maps to NM_000305.2 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:95034734 C>T maps to NM_000305.2 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:100685697 C>A maps to NM_001040105.1 I3667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:100685697 C>A maps to NM_001040105.1 I3667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:101837128 A>T maps to ENST00000360264 K373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:101837128 A>T maps to ENST00000360264 K373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:103234158 G>T maps to ENST00000428762 T1294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:103234158 G>T maps to ENST00000428762 T1294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:107115362 T>A maps to NM_005295.2 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:107115362 T>A maps to NM_005295.2 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:113519931 T>C maps to NM_002711.3 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:113519931 T>C maps to NM_002711.3 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:141424932 C>A maps to NM_001105558.1 I443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:141424932 C>A maps to NM_001105558.1 I443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:141803073 G>A maps to ENST00000475668 T2674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr7:141803073 G>A maps to ENST00000475668 T2674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:35588528 G>A did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:35588528 G>A did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:42294988 C>A maps to NM_006749.3 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:42294988 C>A maps to NM_006749.3 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:77618581 C>A maps to NM_024721.4 C753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:77618581 C>A maps to NM_024721.4 C753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:100866326 G>A maps to NM_017890.3 L3595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:100866326 G>A maps to NM_017890.3 L3595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:110425732 C>T maps to ENST00000426474 S773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:110425732 C>T maps to ENST00000426474 S773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:120602743 C>A did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:120602743 C>A did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:121240970 A>T maps to NM_021110.1 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:121240970 A>T maps to NM_021110.1 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:144877206 C>A did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr8:144877206 C>A did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr9:77257705 A>G maps to ENST00000396204 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr9:77257705 A>G maps to ENST00000396204 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr9:121930237 C>T maps to NM_014618.2 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr9:121930237 C>T maps to NM_014618.2 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr9:136380684 G>A maps to NM_001080483.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr9:136380684 G>A maps to NM_001080483.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chrX:1407467 C>T maps to NM_001161530.1 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chrX:1407467 C>T maps to NM_001161530.1 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chrX:6069248 G>T maps to ENST00000381093 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chrX:6069248 G>T maps to ENST00000381093 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chrX:30260671 C>T maps to NM_002367.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chrX:30260671 C>T maps to NM_002367.3 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chrX:64959589 G>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chrX:64959589 G>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chrX:65824894 C>T maps to ENST00000450752 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chrX:65824894 C>T maps to ENST00000450752 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chrX:73961160 A>G maps to NM_001008537.2 P1077P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chrX:73961160 A>G maps to NM_001008537.2 P1077P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chrX:83616509 C>G maps to NM_144657.4 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chrX:83616509 C>G maps to NM_144657.4 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chrX:102003884 G>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chrX:102003884 G>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chrX:104478564 G>A maps to NM_017416.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chrX:104478564 G>A maps to NM_017416.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chrY:22930713 G>A maps to NM_001039567.2 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chrY:22930713 G>A maps to NM_001039567.2 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr1:23520574 G>A maps to NM_000864.4 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr1:23520574 G>A maps to NM_000864.4 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr1:152281223 G>A maps to NM_002016.1 D2046D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr1:152281223 G>A maps to NM_002016.1 D2046D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr1:201751709 A>T maps to ENST00000367296 G690G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr1:201751709 A>T maps to ENST00000367296 G690G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr10:95111311 A>T maps to NM_013451.3 L1227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr10:95111311 A>T maps to NM_013451.3 L1227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr12:81693144 C>A maps to NM_003625.2 E887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr12:81693144 C>A maps to NM_003625.2 E887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr13:38320379 G>C maps to NM_003306.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr13:38320379 G>C maps to NM_003306.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr14:23746103 A>G maps to NM_020834.2 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr14:23746103 A>G maps to NM_020834.2 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr17:28645839 C>T maps to NM_206832.1 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr17:28645839 C>T maps to NM_206832.1 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr17:40761275 G>A maps to NM_178126.3 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr17:40761275 G>A maps to NM_178126.3 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr19:37210996 C>A maps to ENST00000423498 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr19:37210996 C>A maps to ENST00000423498 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr19:45768122 G>A maps to NM_031417.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr19:45768122 G>A maps to NM_031417.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr2:21228714 G>T maps to NM_000384.2 I3675I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr2:21228714 G>T maps to NM_000384.2 I3675I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr2:136499549 G>A maps to NM_014607.3 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr2:136499549 G>A maps to NM_014607.3 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr2:238726674 C>G maps to NM_001080504.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr2:238726674 C>G maps to NM_001080504.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr20:32212734 C>T maps to NM_005093.3 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr20:32212734 C>T maps to NM_005093.3 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr20:37144952 C>T maps to NM_020336.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr20:37144952 C>T maps to NM_020336.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr21:36206845 G>A maps to NM_001754.4 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr21:36206845 G>A maps to NM_001754.4 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr3:27490192 T>A maps to ENST00000454389 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr3:27490192 T>A maps to ENST00000454389 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr3:44612215 C>G maps to NM_018651.2 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr3:44612215 C>G maps to NM_018651.2 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr3:107941067 G>T maps to ENST00000457963 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr3:107941067 G>T maps to ENST00000457963 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr3:128060188 C>T maps to NM_021937.3 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr3:128060188 C>T maps to NM_021937.3 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr3:130292956 C>T maps to NM_001102608.1 S1045S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr3:130292956 C>T maps to NM_001102608.1 S1045S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr5:101606379 T>A maps to NM_180991.4 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr5:101606379 T>A maps to NM_180991.4 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr5:118469799 G>A maps to NM_005509.4 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr5:118469799 G>A maps to NM_005509.4 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr7:45956910 T>C maps to NM_001013398.1 K183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr7:45956910 T>C maps to NM_001013398.1 K183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr7:86415677 C>T maps to NM_000840.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr7:86415677 C>T maps to NM_000840.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr9:140919616 C>T maps to ENST00000277549 V1094V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr9:140919616 C>T maps to ENST00000277549 V1094V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chrX:15268557 C>A maps to NM_001031739.2 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chrX:15268557 C>A maps to NM_001031739.2 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chrX:123164833 C>T maps to NM_001042750.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chrX:123164833 C>T maps to NM_001042750.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr1:75172794 G>A maps to NM_001889.3 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr1:75172794 G>A maps to NM_001889.3 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr1:152187689 T>A maps to NM_001009931.1 R2139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr1:152187689 T>A maps to NM_001009931.1 R2139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr1:201012530 G>T maps to NM_000069.2 V1642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr1:201012530 G>T maps to NM_000069.2 V1642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr10:15138709 C>T maps to NM_153244.1 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr10:15138709 C>T maps to NM_153244.1 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr10:97917660 G>T maps to NM_014803.3 E528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr10:97917660 G>T maps to NM_014803.3 E528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr11:31671744 A>G maps to ENST00000395934 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr11:31671744 A>G maps to ENST00000395934 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr11:46903410 G>A maps to ENST00000256991 R931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr11:46903410 G>A maps to ENST00000256991 R931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr11:108350192 G>T maps to NM_153705.4 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr11:108350192 G>T maps to NM_153705.4 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr12:124798974 C>A maps to ENST00000389727 C185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr12:124798974 C>A maps to ENST00000389727 C185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr13:99554562 G>A maps to ENST00000428223 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr13:99554562 G>A maps to ENST00000428223 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr14:91142992 G>A maps to NM_001010854.1 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr14:91142992 G>A maps to NM_001010854.1 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr15:102358821 T>C maps to NM_001001674.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr15:102358821 T>C maps to NM_001001674.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr16:30510406 G>A maps to NM_002209.2 V615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr16:30510406 G>A maps to NM_002209.2 V615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr16:67700070 G>A maps to NM_032140.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr16:67700070 G>A maps to NM_032140.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr17:7099546 G>A maps to NM_001365.3 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr17:7099546 G>A maps to NM_001365.3 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr17:37368613 G>A maps to NM_198993.3 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr17:37368613 G>A maps to NM_198993.3 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr17:78899183 G>A maps to NM_020761.2 A941A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr17:78899183 G>A maps to NM_020761.2 A941A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr19:36214908 G>T did not map to a codon.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr19:36214908 G>T did not map to a codon.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr19:52856993 G>C maps to NM_001161425.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr19:52856993 G>C maps to NM_001161425.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr19:54745722 C>A maps to ENST00000270464 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr19:54745722 C>A maps to ENST00000270464 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr2:80620358 T>C maps to ENST00000402739 D360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr2:80620358 T>C maps to ENST00000402739 D360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr2:160585575 C>T maps to NM_022826.2 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr2:160585575 C>T maps to NM_022826.2 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr2:179979881 C>A maps to NM_178123.4 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr2:179979881 C>A maps to NM_178123.4 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr20:36631032 C>T maps to NM_014657.1 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr20:36631032 C>T maps to NM_014657.1 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr21:31538656 G>A maps to NM_012131.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr21:31538656 G>A maps to NM_012131.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr3:6903212 G>A maps to NM_181874.2 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr3:6903212 G>A maps to NM_181874.2 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr3:126708595 G>A maps to NM_032242.3 W387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr3:126708595 G>A maps to NM_032242.3 W387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr3:142098953 G>A maps to NM_019001.3 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr3:142098953 G>A maps to NM_019001.3 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr3:184101431 T>C did not map to a codon.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr3:184101431 T>C did not map to a codon.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr4:111430848 G>A maps to NM_001977.3 E360E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr4:111430848 G>A maps to NM_001977.3 E360E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr5:161524780 C>T maps to NM_198903.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr5:161524780 C>T maps to NM_198903.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr6:56489976 G>T maps to ENST00000361203 S1392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr6:56489976 G>T maps to ENST00000361203 S1392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr6:106552716 C>T maps to NM_001198.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr6:106552716 C>T maps to NM_001198.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr6:157528079 G>A maps to ENST00000367148 A1975A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr6:157528079 G>A maps to ENST00000367148 A1975A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr7:51203959 C>T maps to ENST00000395542 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr7:51203959 C>T maps to ENST00000395542 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr7:100696278 G>A maps to NM_001040105.1 T4372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr7:100696278 G>A maps to NM_001040105.1 T4372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr7:149510809 C>T maps to NM_198455.2 C3368C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr7:149510809 C>T maps to NM_198455.2 C3368C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr9:100424348 G>A maps to NM_002486.4 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr9:100424348 G>A maps to NM_002486.4 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:1417590 C>T maps to NM_031921.4 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:1417590 C>T maps to NM_031921.4 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:3427383 G>A maps to ENST00000452816 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:3427383 G>A maps to ENST00000452816 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:16464403 G>C maps to NM_004431.3 S419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:16464403 G>C maps to NM_004431.3 S419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:27272171 G>A maps to NM_006600.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:27272171 G>A maps to NM_006600.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:67558948 G>C maps to NM_001013674.1 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:67558948 G>C maps to NM_001013674.1 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:70505166 G>C maps to NM_020794.2 V1182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:70505166 G>C maps to NM_020794.2 V1182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:111990151 G>A maps to NM_024102.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:111990151 G>A maps to NM_024102.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:151317304 C>A maps to NM_000449.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:151317304 C>A maps to NM_000449.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:153533965 G>A maps to ENST00000368707 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:153533965 G>A maps to ENST00000368707 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:155629558 C>T maps to ENST00000368339 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:155629558 C>T maps to ENST00000368339 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:159015212 C>T maps to ENST00000295809 Q486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:159015212 C>T maps to ENST00000295809 Q486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:165322353 G>A maps to NM_177398.3 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:165322353 G>A maps to NM_177398.3 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:200801915 G>A maps to ENST00000236925 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:200801915 G>A maps to ENST00000236925 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:249211311 C>T maps to NM_170725.2 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr1:249211311 C>T maps to NM_170725.2 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:5495244 C>T maps to NM_001047160.1 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:5495244 C>T maps to NM_001047160.1 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:16957876 G>A maps to NM_001081.3 Q2385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:16957876 G>A maps to NM_001081.3 Q2385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:22208790 G>C maps to NM_022365.3 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:22208790 G>C maps to NM_022365.3 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:76789240 C>T maps to NM_012330.2 S1553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:76789240 C>T maps to NM_012330.2 S1553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:99655056 G>A maps to NM_018058.4 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:99655056 G>A maps to NM_018058.4 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:106152106 G>C maps to NM_001008723.1 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:106152106 G>C maps to NM_001008723.1 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:129207595 G>A maps to ENST00000398025 V1473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:129207595 G>A maps to ENST00000398025 V1473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:133946814 G>C did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr10:133946814 G>C did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:479109 G>C maps to NM_030783.1 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:479109 G>C maps to NM_030783.1 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:605231 G>A maps to ENST00000264555 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:605231 G>A maps to ENST00000264555 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:12263801 C>G maps to NM_014632.2 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:12263801 C>G maps to NM_014632.2 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:13427227 C>T maps to NM_032320.5 Q328Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:13427227 C>T maps to NM_032320.5 Q328Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:14539456 G>C maps to NM_148976.2 S46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:14539456 G>C maps to NM_148976.2 S46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:59211186 C>T maps to NM_001004728.1 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:59211186 C>T maps to NM_001004728.1 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:63767134 C>T maps to NM_014067.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:63767134 C>T maps to NM_014067.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:64054130 C>G maps to NM_001170726.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:64054130 C>G maps to NM_001170726.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:64510266 G>A maps to ENST00000320253 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:64510266 G>A maps to ENST00000320253 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:65635367 G>T maps to NM_016938.3 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:65635367 G>T maps to NM_016938.3 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:72290598 G>T maps to NM_002599.3 I745I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:72290598 G>T maps to NM_002599.3 I745I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:103047051 G>C maps to NM_001080463.1 L1921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:103047051 G>C maps to NM_001080463.1 L1921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:118239344 G>C did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:118239344 G>C did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:126110785 C>G maps to NM_024556.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr11:126110785 C>G maps to NM_024556.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:6103291 G>A maps to NM_000552.3 Q2112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:6103291 G>A maps to NM_000552.3 Q2112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:6103364 G>T maps to NM_000552.3 I2087I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:6103364 G>T maps to NM_000552.3 I2087I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:12940237 G>A maps to NM_001130415.1 E164E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:12940237 G>A maps to NM_001130415.1 E164E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:21680691 G>C maps to NM_030572.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:21680691 G>C maps to NM_030572.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:57924486 C>T maps to ENST00000434715 K402K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:57924486 C>T maps to ENST00000434715 K402K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:100657383 C>A maps to ENST00000422147 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:100657383 C>A maps to ENST00000422147 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:103248920 G>A maps to NM_000277.1 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:103248920 G>A maps to NM_000277.1 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:109629725 C>T maps to NM_001093.3 C790C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:109629725 C>T maps to NM_001093.3 C790C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:112699140 G>A maps to NM_001109662.2 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:112699140 G>A maps to NM_001109662.2 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:121448688 G>A maps to NM_022895.1 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:121448688 G>A maps to NM_022895.1 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:122962394 G>A maps to NM_017612.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:122962394 G>A maps to NM_017612.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:123810856 G>A maps to NM_001167856.1 Q573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr12:123810856 G>A maps to NM_001167856.1 Q573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr13:20797247 C>T maps to NM_001110221.2 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr13:20797247 C>T maps to NM_001110221.2 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr13:29001375 C>A maps to NM_002019.4 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr13:29001375 C>A maps to NM_002019.4 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr13:30804673 G>A maps to NM_032116.3 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr13:30804673 G>A maps to NM_032116.3 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr13:41894878 C>G maps to NM_024561.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr13:41894878 C>G maps to NM_024561.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr13:95858998 G>A maps to NM_005845.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr13:95858998 G>A maps to NM_005845.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr13:98086810 C>T maps to NM_021033.6 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr13:98086810 C>T maps to NM_021033.6 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr14:23884361 C>A maps to NM_000257.2 E1801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr14:23884361 C>A maps to NM_000257.2 E1801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr14:35593113 C>T maps to NM_014672.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr14:35593113 C>T maps to NM_014672.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr14:57082693 C>A maps to NM_017799.3 S297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr14:57082693 C>A maps to NM_017799.3 S297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr14:57699410 G>C maps to ENST00000340918 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr14:57699410 G>C maps to ENST00000340918 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr15:45415128 G>A maps to NM_144565.2 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr15:45415128 G>A maps to NM_144565.2 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr15:50830916 G>A maps to ENST00000456636 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr15:50830916 G>A maps to ENST00000456636 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr15:72691139 A>G maps to NM_001080462.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr15:72691139 A>G maps to NM_001080462.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr15:75047130 G>C did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr15:75047130 G>C did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr15:77907917 C>A maps to NM_032808.5 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr15:77907917 C>A maps to NM_032808.5 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:706410 C>G maps to NM_145294.4 Y692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:706410 C>G maps to NM_145294.4 Y692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:836893 G>A maps to NM_058192.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:836893 G>A maps to NM_058192.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:2547030 C>T maps to ENST00000434757 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:2547030 C>T maps to ENST00000434757 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:29934633 G>C maps to NM_178863.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:29934633 G>C maps to NM_178863.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:57761224 G>A maps to NM_032269.5 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:57761224 G>A maps to NM_032269.5 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:66975678 G>A maps to NM_003869.5 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:66975678 G>A maps to NM_003869.5 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:67469872 C>T maps to NM_000196.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:67469872 C>T maps to NM_000196.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:75203754 C>T maps to NM_153688.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:75203754 C>T maps to NM_153688.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:81145965 G>A maps to NM_052892.3 F2261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:81145965 G>A maps to NM_052892.3 F2261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:88925145 C>A maps to NM_016209.3 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr16:88925145 C>A maps to NM_016209.3 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:7259354 T>C maps to NM_198154.1 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:7259354 T>C maps to NM_198154.1 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:17898416 C>A maps to NM_031294.3 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:17898416 C>A maps to NM_031294.3 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:21208406 C>T maps to NM_145109.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:21208406 C>T maps to NM_145109.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:29220739 G>A maps to NM_024857.3 K1623K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:29220739 G>A maps to NM_024857.3 K1623K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:38567941 T>C maps to ENST00000357601 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:38567941 T>C maps to ENST00000357601 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:41599573 C>T maps to NM_004941.1 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:41599573 C>T maps to NM_004941.1 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:43517534 G>A maps to NM_014798.2 L965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:43517534 G>A maps to NM_014798.2 L965L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:56342210 C>G maps to NM_006151.2 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:56342210 C>G maps to NM_006151.2 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:56440746 C>T maps to NM_017763.4 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:56440746 C>T maps to NM_017763.4 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:67150090 G>A maps to NM_080282.3 F1282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:67150090 G>A maps to NM_080282.3 F1282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:72469963 C>T maps to NM_007261.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:72469963 C>T maps to NM_007261.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:74071152 C>T maps to NM_003857.2 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:74071152 C>T maps to NM_003857.2 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:74071275 C>T maps to NM_003857.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:74071275 C>T maps to NM_003857.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:74475232 C>T maps to NM_024599.5 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:74475232 C>T maps to NM_024599.5 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:75398525 C>T maps to NM_001113491.1 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr17:75398525 C>T maps to NM_001113491.1 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr18:22805753 G>A maps to NM_015461.2 Q710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr18:22805753 G>A maps to NM_015461.2 Q710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:621365 C>A maps to NM_005035.3 E778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:621365 C>A maps to NM_005035.3 E778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:1818553 G>A maps to NM_020695.3 L981L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:1818553 G>A maps to NM_020695.3 L981L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:10395702 C>T maps to NM_000201.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:10395702 C>T maps to NM_000201.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:11354275 C>T maps to ENST00000319867 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:11354275 C>T maps to ENST00000319867 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:38853161 C>T maps to NM_021185.4 F768F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:38853161 C>T maps to NM_021185.4 F768F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:42737443 G>A maps to NM_019884.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:42737443 G>A maps to NM_019884.2 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:48229327 C>T maps to NM_014601.3 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:48229327 C>T maps to NM_014601.3 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:50721023 G>T maps to NM_001145809.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:50721023 G>T maps to NM_001145809.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:51958027 G>C maps to NM_014442.2 S353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr19:51958027 G>C maps to NM_014442.2 S353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:23980729 G>A maps to NM_017552.1 I1212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:23980729 G>A maps to NM_017552.1 I1212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:24255768 G>A maps to NM_025203.2 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:24255768 G>A maps to NM_025203.2 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:27566300 C>A maps to NM_001521.2 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:27566300 C>A maps to NM_001521.2 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:29063066 C>T maps to NM_182756.3 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:29063066 C>T maps to NM_182756.3 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:29294901 C>T maps to NM_001029883.1 E742E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:29294901 C>T maps to NM_001029883.1 E742E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:31598257 C>T maps to NM_000379.3 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:31598257 C>T maps to NM_000379.3 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:43902888 C>T maps to NM_001101330.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:43902888 C>T maps to NM_001101330.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:46770214 C>T maps to NM_012249.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:46770214 C>T maps to NM_012249.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:54852071 G>A maps to NM_003128.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:54852071 G>A maps to NM_003128.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:73303222 C>T maps to NM_015470.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:73303222 C>T maps to NM_015470.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:73959361 G>C maps to ENST00000409716 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:73959361 G>C maps to ENST00000409716 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:143790865 C>G maps to NM_003937.2 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:143790865 C>G maps to NM_003937.2 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:170115653 G>T maps to NM_004525.2 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:170115653 G>T maps to NM_004525.2 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:202625888 G>A maps to NM_020919.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:202625888 G>A maps to NM_020919.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:219222440 C>T maps to NM_198559.1 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:219222440 C>T maps to NM_198559.1 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:232576620 G>T maps to ENST00000409321 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr2:232576620 G>T maps to ENST00000409321 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr20:2474451 C>T maps to NM_024325.4 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr20:2474451 C>T maps to NM_024325.4 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr20:3529963 C>G maps to NM_139321.2 S364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr20:3529963 C>G maps to NM_139321.2 S364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr20:31647252 G>A maps to NM_182658.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr20:31647252 G>A maps to NM_182658.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr20:43251499 G>A maps to NM_000022.2 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr20:43251499 G>A maps to NM_000022.2 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr20:61846953 C>G did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr20:61846953 C>G did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr20:62038283 C>A maps to NM_172107.2 E778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr20:62038283 C>A maps to NM_172107.2 E778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr21:41684116 C>G maps to NM_001389.3 T651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr21:41684116 C>G maps to NM_001389.3 T651T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr22:38202087 G>A maps to NM_005318.3 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr22:38202087 G>A maps to NM_005318.3 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr22:41613199 C>T maps to NM_031488.4 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr22:41613199 C>T maps to NM_031488.4 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr22:41925316 C>T maps to NM_138338.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr22:41925316 C>T maps to NM_138338.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:9990497 G>C maps to NM_207351.3 S372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:9990497 G>C maps to NM_207351.3 S372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:10188210 C>T maps to NM_000551.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:10188210 C>T maps to NM_000551.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:10392201 G>A maps to NM_001001331.2 G732G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:10392201 G>A maps to NM_001001331.2 G732G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:12983122 G>C maps to ENST00000429247 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:12983122 G>C maps to ENST00000429247 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:15686311 C>T maps to NM_000060.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:15686311 C>T maps to NM_000060.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:33155700 C>T maps to NM_006371.4 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:33155700 C>T maps to NM_006371.4 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:38266072 G>A maps to NM_005109.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:38266072 G>A maps to NM_005109.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:48625736 G>A maps to NM_000094.3 F896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:48625736 G>A maps to NM_000094.3 F896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:48626387 G>A maps to NM_000094.3 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:48626387 G>A maps to NM_000094.3 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:49692475 C>G maps to NM_003458.3 L1829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:49692475 C>G maps to NM_003458.3 L1829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:49936567 C>T maps to NM_002447.2 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:49936567 C>T maps to NM_002447.2 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:55717820 C>G did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:55717820 C>G did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:70014320 C>T maps to ENST00000448226 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:70014320 C>T maps to ENST00000448226 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:97711818 G>C maps to NM_001105580.1 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:97711818 G>C maps to NM_001105580.1 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:98512550 C>G maps to ENST00000493584 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:98512550 C>G maps to ENST00000493584 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:130300642 G>C maps to NM_001102608.1 L1262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:130300642 G>C maps to NM_001102608.1 L1262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:143691431 C>G maps to NM_173552.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:143691431 C>G maps to NM_173552.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:151155922 C>T maps to NM_178822.4 R2142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:151155922 C>T maps to NM_178822.4 R2142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:189586431 G>A maps to NM_003722.4 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr3:189586431 G>A maps to NM_003722.4 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr4:41016113 G>A maps to NM_004307.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr4:41016113 G>A maps to NM_004307.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr4:54364927 G>C maps to NM_001126328.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr4:54364927 G>C maps to NM_001126328.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr4:73149385 G>A maps to NM_014243.1 Q1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr4:73149385 G>A maps to NM_014243.1 Q1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr4:103585970 C>T maps to NM_005908.3 W452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr4:103585970 C>T maps to NM_005908.3 W452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr4:126241933 C>A maps to NM_024582.4 S1456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr4:126241933 C>A maps to NM_024582.4 S1456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:32091008 G>C maps to NM_178140.2 L2485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:32091008 G>C maps to NM_178140.2 L2485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:37479939 C>T maps to NM_018034.2 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:37479939 C>T maps to NM_018034.2 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:66456299 C>G maps to NM_001164664.1 S1222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:66456299 C>G maps to NM_001164664.1 S1222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:81613992 C>T maps to NM_001017971.1 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:81613992 C>T maps to NM_001017971.1 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:92929547 G>C maps to NM_005654.4 *424Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:92929547 G>C maps to NM_005654.4 *424Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:128364097 C>T maps to NM_001017372.1 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:128364097 C>T maps to NM_001017372.1 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:136403476 G>A maps to NM_004598.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:136403476 G>A maps to NM_004598.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:136964010 G>A maps to NM_017415.2 D522D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:136964010 G>A maps to NM_017415.2 D522D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:137028127 G>A maps to NM_017415.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:137028127 G>A maps to NM_017415.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:137754820 G>A maps to NM_016604.3 L1205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:137754820 G>A maps to NM_016604.3 L1205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:142283206 G>T maps to NM_015071.4 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:142283206 G>T maps to NM_015071.4 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:150723126 G>A maps to NM_181776.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:150723126 G>A maps to NM_181776.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:151169927 C>G maps to NM_198395.1 S47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:151169927 C>G maps to NM_198395.1 S47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:168127612 C>G maps to NM_003062.2 L972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:168127612 C>G maps to NM_003062.2 L972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:176026362 G>C maps to NM_052899.2 S158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:176026362 G>C maps to NM_052899.2 S158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:178359094 C>T maps to NM_030613.2 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr5:178359094 C>T maps to NM_030613.2 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:32942322 C>T maps to ENST00000395289 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:32942322 C>T maps to ENST00000395289 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:35280428 G>A maps to NM_022047.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:35280428 G>A maps to NM_022047.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:35888246 C>T maps to ENST00000361690 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:35888246 C>T maps to ENST00000361690 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:36475337 C>T maps to NM_007271.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:36475337 C>T maps to NM_007271.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:38791363 G>C maps to ENST00000327475 L1237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:38791363 G>C maps to ENST00000327475 L1237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:42227371 C>T maps to NM_033502.2 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:42227371 C>T maps to NM_033502.2 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:43480833 G>A maps to ENST00000506469 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:43480833 G>A maps to ENST00000506469 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:46977115 C>T maps to ENST00000283297 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:46977115 C>T maps to ENST00000283297 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:46977148 C>T maps to ENST00000283297 W675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:46977148 C>T maps to ENST00000283297 W675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:46977655 C>G maps to ENST00000283297 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:46977655 C>G maps to ENST00000283297 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:1479681 C>T maps to NM_182924.3 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:1479681 C>T maps to NM_182924.3 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:82583503 A>C maps to NM_033026.5 G2255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:82583503 A>C maps to NM_033026.5 G2255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:87072721 C>T maps to NM_018849.2 Q423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:87072721 C>T maps to NM_018849.2 Q423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:102100193 C>A maps to NM_017621.3 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:102100193 C>A maps to NM_017621.3 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:105146707 G>A maps to NM_019042.3 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:105146707 G>A maps to NM_019042.3 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:135289086 G>C did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:135289086 G>C did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:148495715 G>T maps to NM_003592.2 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:148495715 G>T maps to NM_003592.2 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:148801942 G>A maps to NM_001001661.2 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr7:148801942 G>A maps to NM_001001661.2 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:19297417 C>T maps to NM_018371.4 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:19297417 C>T maps to NM_018371.4 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:24356804 C>T maps to ENST00000380789 C633C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:24356804 C>T maps to ENST00000380789 C633C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:33369603 G>A maps to NM_001102401.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:33369603 G>A maps to NM_001102401.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:48777318 G>T maps to NM_006904.6 S1789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:48777318 G>T maps to NM_006904.6 S1789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:52284540 G>A maps to NM_144651.4 Q1265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:52284540 G>A maps to NM_144651.4 Q1265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:73942627 G>A maps to NM_017489.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:73942627 G>A maps to NM_017489.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:77617903 G>A maps to NM_024721.4 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:77617903 G>A maps to NM_024721.4 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:94746325 G>A maps to NM_203390.2 F771F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:94746325 G>A maps to NM_203390.2 F771F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:102701557 C>T maps to NM_032041.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:102701557 C>T maps to NM_032041.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:144941430 G>A maps to NM_031308.1 L1997L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:144941430 G>A maps to NM_031308.1 L1997L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:146157134 C>T maps to NM_006958.2 E346E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr8:146157134 C>T maps to NM_006958.2 E346E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:4605409 C>T maps to ENST00000454239 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:4605409 C>T maps to ENST00000454239 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:34290295 G>A maps to NM_194313.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:34290295 G>A maps to NM_194313.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:87482317 C>T maps to NM_006180.3 I535I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:87482317 C>T maps to NM_006180.3 I535I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:107298344 G>A maps to NM_001001961.1 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:107298344 G>A maps to NM_001001961.1 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:112899401 C>G maps to NM_007203.4 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:112899401 C>G maps to NM_007203.4 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:114875120 G>C maps to NM_022486.3 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:114875120 G>C maps to NM_022486.3 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:124794103 C>T maps to NM_001139442.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:124794103 C>T maps to NM_001139442.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:135975665 G>C maps to NM_006266.2 S853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:135975665 G>C maps to NM_006266.2 S853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:138391607 C>G maps to NM_001048265.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr9:138391607 C>G maps to NM_001048265.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chrX:9679749 C>T maps to NM_005647.3 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chrX:9679749 C>T maps to NM_005647.3 F513F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chrX:18646648 G>A maps to NM_001037343.1 G885G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chrX:18646648 G>A maps to NM_001037343.1 G885G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chrX:50094304 G>A maps to NM_033031.2 L1342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chrX:50094304 G>A maps to NM_033031.2 L1342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chrX:68058465 G>A maps to NM_004429.4 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chrX:68058465 G>A maps to NM_004429.4 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr1:42046334 G>A maps to NM_024503.3 P1378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr1:42046334 G>A maps to NM_024503.3 P1378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr1:178491562 T>A maps to NM_032126.4 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr1:178491562 T>A maps to NM_032126.4 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr14:64493343 C>T maps to NM_182914.2 I2100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr14:64493343 C>T maps to NM_182914.2 I2100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr14:105414122 A>G maps to NM_138420.2 P2555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr14:105414122 A>G maps to NM_138420.2 P2555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr16:50820853 A>T maps to ENST00000311559 K680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr16:50820853 A>T maps to ENST00000311559 K680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr18:13645457 C>G maps to NM_181481.3 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr18:13645457 C>G maps to NM_181481.3 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr19:21719157 G>A maps to NM_001001415.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr19:21719157 G>A maps to NM_001001415.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr4:48529996 C>T maps to NM_015030.1 K2377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr4:48529996 C>T maps to NM_015030.1 K2377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr5:140480301 G>A maps to NM_018937.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr5:140480301 G>A maps to NM_018937.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr6:31828218 G>A maps to NM_000434.3 C265C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr6:31828218 G>A maps to NM_000434.3 C265C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr8:55534065 C>T maps to NM_006269.1 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr8:55534065 C>T maps to NM_006269.1 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr9:111795699 A>G maps to NM_032012.3 P827P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5153-01A-01D-1434-08 chr9:111795699 A>G maps to NM_032012.3 P827P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr1:17743044 C>T maps to NM_018715.2 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr1:17743044 C>T maps to NM_018715.2 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr1:33820074 C>T maps to ENST00000419414 Q495Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr1:33820074 C>T maps to ENST00000419414 Q495Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr1:155747429 G>A maps to ENST00000368331 Q692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr1:155747429 G>A maps to ENST00000368331 Q692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr1:176668368 G>T maps to NM_020318.2 P960P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr1:176668368 G>T maps to NM_020318.2 P960P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr1:196928026 A>G maps to ENST00000367421 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr1:196928026 A>G maps to ENST00000367421 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr11:62294808 T>C maps to NM_001620.1 V2360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr11:62294808 T>C maps to NM_001620.1 V2360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr11:71293826 G>A maps to ENST00000376535 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr11:71293826 G>A maps to ENST00000376535 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr11:130058528 C>T maps to NM_021978.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr11:130058528 C>T maps to NM_021978.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr12:9162051 C>A maps to NM_005810.3 C163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr12:9162051 C>A maps to NM_005810.3 C163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr12:71158498 T>G maps to NM_002849.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr12:71158498 T>G maps to NM_002849.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr12:81472118 G>T maps to NM_024560.2 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr12:81472118 G>T maps to NM_024560.2 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr12:95660257 T>A maps to NM_017599.3 L187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr12:95660257 T>A maps to NM_017599.3 L187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr12:107126786 C>G maps to ENST00000357881 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr12:107126786 C>G maps to ENST00000357881 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr14:20849088 C>T did not map to a codon.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr14:20849088 C>T did not map to a codon.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr15:41795315 G>A maps to NM_002220.1 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr15:41795315 G>A maps to NM_002220.1 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr16:21995734 C>A maps to ENST00000424898 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr16:21995734 C>A maps to ENST00000424898 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr16:70852358 C>T maps to NM_032821.2 A4847A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr16:70852358 C>T maps to NM_032821.2 A4847A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr17:80041947 G>A maps to NM_004104.4 P1667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr17:80041947 G>A maps to NM_004104.4 P1667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr18:13069787 A>T maps to NM_032142.3 K1703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr18:13069787 A>T maps to NM_032142.3 K1703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr19:39281520 C>T maps to NM_001042507.3 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr19:39281520 C>T maps to NM_001042507.3 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr19:40327294 C>A maps to NM_001436.3 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr19:40327294 C>A maps to NM_001436.3 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr2:108863793 T>C maps to NM_001008743.1 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr2:108863793 T>C maps to NM_001008743.1 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr20:39706250 G>A maps to NM_003286.2 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr20:39706250 G>A maps to NM_003286.2 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr20:43933063 C>T maps to ENST00000372754 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr20:43933063 C>T maps to ENST00000372754 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr20:47991214 G>A maps to NM_004975.2 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr20:47991214 G>A maps to NM_004975.2 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr22:33253267 G>C maps to NM_000362.4 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr22:33253267 G>C maps to NM_000362.4 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr22:50591607 G>A maps to NM_018995.2 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr22:50591607 G>A maps to NM_018995.2 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr4:22749648 T>A maps to NM_020973.3 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr4:22749648 T>A maps to NM_020973.3 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr4:177113892 G>A maps to NM_144644.2 N191N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr4:177113892 G>A maps to NM_144644.2 N191N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr5:423992 G>A maps to NM_020731.3 Q207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr5:423992 G>A maps to NM_020731.3 Q207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr5:45262155 G>T maps to NM_021072.2 S847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr5:45262155 G>T maps to NM_021072.2 S847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr5:176637761 C>T maps to NM_022455.4 R788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr5:176637761 C>T maps to NM_022455.4 R788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr6:32188356 G>A maps to NM_004557.3 N328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr6:32188356 G>A maps to NM_004557.3 N328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr6:34827075 C>T maps to NM_017754.3 S981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr6:34827075 C>T maps to NM_017754.3 S981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr6:57012575 G>T maps to NM_001031623.2 E565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr6:57012575 G>T maps to NM_001031623.2 E565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr6:100390919 C>A maps to NM_032503.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr6:100390919 C>A maps to NM_032503.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr7:32338305 G>T maps to NM_001191058.1 C14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr7:32338305 G>T maps to NM_001191058.1 C14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr7:94879415 G>T maps to NM_001166160.1 E749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr7:94879415 G>T maps to NM_001166160.1 E749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr7:130038841 T>A maps to NM_018718.1 K338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr7:130038841 T>A maps to NM_018718.1 K338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr8:73480043 G>T maps to NM_004770.2 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr8:73480043 G>T maps to NM_004770.2 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr8:100829988 G>T maps to NM_017890.3 V2798V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr8:100829988 G>T maps to NM_017890.3 V2798V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr8:144893220 C>T maps to NM_182706.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5555-01A-01D-1512-08 chr8:144893220 C>T maps to NM_182706.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr1:24202068 G>C maps to NM_001841.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr1:24202068 G>C maps to NM_001841.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr1:36755246 G>T maps to NM_005119.3 E543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr1:36755246 G>T maps to NM_005119.3 E543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr1:53543412 C>T maps to NM_153703.4 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr1:53543412 C>T maps to NM_153703.4 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr1:100736124 C>T maps to NM_001130841.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr1:100736124 C>T maps to NM_001130841.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr1:109342873 A>G maps to NM_007269.2 E494E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr1:109342873 A>G maps to NM_007269.2 E494E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr1:230845930 C>T maps to NM_000029.3 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr1:230845930 C>T maps to NM_000029.3 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr11:1087950 C>T maps to ENST00000441003 F1142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr11:1087950 C>T maps to ENST00000441003 F1142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr11:3845336 C>T maps to NM_014489.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr11:3845336 C>T maps to NM_014489.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr11:22249036 G>T maps to NM_213599.2 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr11:22249036 G>T maps to NM_213599.2 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr11:47330540 A>G maps to NM_003682.3 K1293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr11:47330540 A>G maps to NM_003682.3 K1293K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr11:59244958 G>A maps to NM_001004705.1 Q19Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr11:59244958 G>A maps to NM_001004705.1 Q19Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr11:64536791 G>A maps to NM_201995.2 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr11:64536791 G>A maps to NM_201995.2 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr12:15262343 G>A maps to NM_032918.2 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr12:15262343 G>A maps to NM_032918.2 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr12:46316326 T>C maps to NM_004719.2 K1388K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr12:46316326 T>C maps to NM_004719.2 K1388K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr12:121431329 C>T maps to NM_000545.5 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr12:121431329 C>T maps to NM_000545.5 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr13:88329622 G>A maps to NM_015567.1 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr13:88329622 G>A maps to NM_015567.1 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr14:50863887 A>T maps to ENST00000356146 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr14:50863887 A>T maps to ENST00000356146 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr14:76642982 T>G maps to NM_017926.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr14:76642982 T>G maps to NM_017926.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr14:94711995 C>T maps to NM_058237.1 Q473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr14:94711995 C>T maps to NM_058237.1 Q473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr15:24923845 T>C maps to NM_018958.2 G944G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr15:24923845 T>C maps to NM_018958.2 G944G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr15:90328693 G>A maps to NM_001150.2 F930F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr15:90328693 G>A maps to NM_001150.2 F930F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr17:44109630 G>A maps to NM_015443.3 Q958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr17:44109630 G>A maps to NM_015443.3 Q958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr19:22155687 A>T maps to NM_007153.3 T716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr19:22155687 A>T maps to NM_007153.3 T716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr19:40928871 G>C maps to NM_013376.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr19:40928871 G>C maps to NM_013376.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr19:45561106 G>A maps to NM_007056.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr19:45561106 G>A maps to NM_007056.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr19:46032621 G>A maps to NM_001017989.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr19:46032621 G>A maps to NM_001017989.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr19:46664117 C>T maps to NM_001002915.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr19:46664117 C>T maps to NM_001002915.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr2:202149859 C>G maps to NM_001080125.1 S434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr2:202149859 C>G maps to NM_001080125.1 S434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr21:27269977 C>T maps to NM_000484.3 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr21:27269977 C>T maps to NM_000484.3 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr22:41257197 C>T maps to NM_145174.1 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr22:41257197 C>T maps to NM_145174.1 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr3:37555267 C>T maps to NM_002207.2 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr3:37555267 C>T maps to NM_002207.2 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr3:56681251 C>A did not map to a codon.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr3:56681251 C>A did not map to a codon.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr3:142388319 C>T maps to NM_001172312.1 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr3:142388319 C>T maps to NM_001172312.1 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr4:79285131 C>T maps to NM_025074.6 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr4:79285131 C>T maps to NM_025074.6 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr5:41018009 G>A maps to ENST00000296803 T943T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr5:41018009 G>A maps to ENST00000296803 T943T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr5:102487034 A>T maps to ENST00000451606 K329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr5:102487034 A>T maps to ENST00000451606 K329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr7:110762918 C>A maps to NM_018334.4 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr7:110762918 C>A maps to NM_018334.4 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr8:139601675 G>A maps to NM_152888.1 P1567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr8:139601675 G>A maps to NM_152888.1 P1567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr9:34255734 C>T maps to NM_194313.2 A1290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr9:34255734 C>T maps to NM_194313.2 A1290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr9:140087089 G>A maps to NM_001128228.2 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chr9:140087089 G>A maps to NM_001128228.2 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chrX:12701660 C>A maps to ENST00000429478 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chrX:12701660 C>A maps to ENST00000429478 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chrX:70349994 T>C maps to ENST00000333646 Y1326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chrX:70349994 T>C maps to ENST00000333646 Y1326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chrX:77224508 G>A maps to NM_001029891.2 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5556-01A-01D-1512-08 chrX:77224508 G>A maps to NM_001029891.2 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr1:218609453 G>A maps to NM_001135599.2 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr1:218609453 G>A maps to NM_001135599.2 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr1:248436657 G>A maps to NM_001004695.1 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr1:248436657 G>A maps to NM_001004695.1 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr11:55904528 A>T maps to NM_001004064.1 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr11:55904528 A>T maps to NM_001004064.1 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr11:66278498 G>A maps to NM_024649.4 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr11:66278498 G>A maps to NM_024649.4 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr12:4920107 T>C maps to NM_002235.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr12:4920107 T>C maps to NM_002235.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr12:9318712 C>A maps to NM_002864.2 G731G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr12:9318712 C>A maps to NM_002864.2 G731G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr15:74368257 C>T maps to NM_001038640.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr15:74368257 C>T maps to NM_001038640.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr16:48211015 G>A maps to NM_032583.3 V1119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr16:48211015 G>A maps to NM_032583.3 V1119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr17:5012302 C>T maps to NM_014519.2 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr17:5012302 C>T maps to NM_014519.2 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr17:7578246 A>T maps to NM_001126112.1 L201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr17:7578246 A>T maps to NM_001126112.1 L201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr17:29557871 A>G maps to NM_001042492.2 V1042V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr17:29557871 A>G maps to NM_001042492.2 V1042V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr19:49261275 G>A maps to NM_019113.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr19:49261275 G>A maps to NM_019113.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr19:55623922 G>A maps to NM_017607.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr19:55623922 G>A maps to NM_017607.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr2:179659933 A>G maps to NM_133378.4 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr2:179659933 A>G maps to NM_133378.4 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr20:10626067 G>A maps to NM_000214.2 R683R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr20:10626067 G>A maps to NM_000214.2 R683R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr20:34519276 G>A maps to NM_016436.4 K737K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr20:34519276 G>A maps to NM_016436.4 K737K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr5:96222494 T>A did not map to a codon.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chr5:96222494 T>A did not map to a codon.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chrX:65411984 A>C maps to NM_138737.3 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chrX:65411984 A>C maps to NM_138737.3 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chrX:118797578 C>T maps to ENST00000394612 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chrX:118797578 C>T maps to ENST00000394612 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chrX:154467051 G>C did not map to a codon.
Sequencing variant TCGA-BA-5557-01A-01D-1512-08 chrX:154467051 G>C did not map to a codon.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:3342264 G>A maps to NM_022114.3 Q1020Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:3342264 G>A maps to NM_022114.3 Q1020Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:16046257 C>T maps to ENST00000420314 Y268Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:16046257 C>T maps to ENST00000420314 Y268Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:19487410 C>T maps to ENST00000375267 Q1802Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:19487410 C>T maps to ENST00000375267 Q1802Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:57254661 G>A maps to NM_001004303.4 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:57254661 G>A maps to NM_001004303.4 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:68659749 G>A maps to NM_024911.6 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:68659749 G>A maps to NM_024911.6 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:149905308 G>A maps to NM_001145862.1 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:149905308 G>A maps to NM_001145862.1 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:154309987 C>A maps to NM_020452.3 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:154309987 C>A maps to NM_020452.3 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:241798756 G>A maps to NM_001821.3 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:241798756 G>A maps to NM_001821.3 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:248059076 C>T maps to NM_001001957.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:248059076 C>T maps to NM_001001957.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr10:12866499 C>T maps to NM_153498.2 H290H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr10:12866499 C>T maps to NM_153498.2 H290H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr10:75331187 G>A maps to NM_152586.3 C77C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr10:75331187 G>A maps to NM_152586.3 C77C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr10:103344391 G>A maps to NM_013274.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr10:103344391 G>A maps to NM_013274.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr10:103344515 G>C maps to NM_013274.3 S245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr10:103344515 G>C maps to NM_013274.3 S245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr10:127414361 C>T maps to ENST00000356792 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr10:127414361 C>T maps to ENST00000356792 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr11:63283756 G>A maps to NM_001142535.1 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr11:63283756 G>A maps to NM_001142535.1 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr11:111385712 G>C maps to NM_207430.2 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr11:111385712 G>C maps to NM_207430.2 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr12:49434324 G>A maps to NM_003482.3 R2410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr12:49434324 G>A maps to NM_003482.3 R2410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr12:69250399 C>T maps to NM_001874.4 Q383Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr12:69250399 C>T maps to NM_001874.4 Q383Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr12:106633143 C>T maps to NM_006825.3 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr12:106633143 C>T maps to NM_006825.3 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr15:85341665 C>G maps to NM_014630.2 L899L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr15:85341665 C>G maps to NM_014630.2 L899L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr15:87097593 T>C maps to NM_152336.2 T894T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr15:87097593 T>C maps to NM_152336.2 T894T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr16:711777 C>T maps to NM_145294.4 I1285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr16:711777 C>T maps to NM_145294.4 I1285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr16:716484 C>T maps to NM_145294.4 L1591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr16:716484 C>T maps to NM_145294.4 L1591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr16:58608532 G>C maps to NM_016284.3 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr16:58608532 G>C maps to NM_016284.3 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr16:70513581 G>A maps to NM_145059.2 *1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr16:70513581 G>A maps to NM_145059.2 *1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr17:7983185 C>G maps to NM_001139.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr17:7983185 C>G maps to NM_001139.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr17:11738199 C>G maps to NM_001372.3 L3164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr17:11738199 C>G maps to NM_001372.3 L3164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr17:74085375 C>T maps to NM_001145297.2 E360E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr17:74085375 C>T maps to NM_001145297.2 E360E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr19:11545747 C>T maps to NM_145045.4 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr19:11545747 C>T maps to NM_145045.4 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr19:48801463 G>T maps to NM_144577.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr19:48801463 G>T maps to NM_144577.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr19:52709300 C>T maps to NM_014225.5 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr19:52709300 C>T maps to NM_014225.5 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr19:55401039 G>A maps to NM_002000.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr19:55401039 G>A maps to NM_002000.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr19:55824412 G>A maps to NM_001085488.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr19:55824412 G>A maps to NM_001085488.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr19:57646829 G>C maps to NM_052882.1 S292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr19:57646829 G>C maps to NM_052882.1 S292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr2:31621532 G>A maps to NM_000379.3 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr2:31621532 G>A maps to NM_000379.3 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr2:33813506 A>G maps to ENST00000395190 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr2:33813506 A>G maps to ENST00000395190 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr2:75921516 C>T maps to NM_003203.4 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr2:75921516 C>T maps to NM_003203.4 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr2:242312557 G>A maps to NM_014808.2 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr2:242312557 G>A maps to NM_014808.2 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr20:1629896 G>A maps to NM_018556.3 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr20:1629896 G>A maps to NM_018556.3 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr20:40979289 G>A maps to ENST00000373198 Q615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr20:40979289 G>A maps to ENST00000373198 Q615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr20:42825778 C>T maps to NM_016470.6 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr20:42825778 C>T maps to NM_016470.6 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr3:100463728 G>A maps to NM_001007565.2 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr3:100463728 G>A maps to NM_001007565.2 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr3:119236072 G>A maps to NM_016589.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr3:119236072 G>A maps to NM_016589.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr3:128755857 G>A maps to NM_024768.2 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr3:128755857 G>A maps to NM_024768.2 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr3:134086482 G>A maps to ENST00000514516 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr3:134086482 G>A maps to ENST00000514516 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr3:141497260 C>T maps to NM_139209.2 C45C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr3:141497260 C>T maps to NM_139209.2 C45C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr3:184043112 G>A maps to NM_001194947.1 T978T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr3:184043112 G>A maps to NM_001194947.1 T978T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr4:26719589 G>A maps to NM_018317.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr4:26719589 G>A maps to NM_018317.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr4:73990773 A>G maps to NM_032217.3 G1116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr4:73990773 A>G maps to NM_032217.3 G1116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr4:110612107 G>A maps to NM_001226.3 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr4:110612107 G>A maps to NM_001226.3 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr4:155256200 C>T maps to NM_017639.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr4:155256200 C>T maps to NM_017639.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr5:115783451 G>A maps to ENST00000257414 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr5:115783451 G>A maps to ENST00000257414 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr5:145379751 C>T maps to NM_152550.3 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr5:145379751 C>T maps to NM_152550.3 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr5:161524717 C>T maps to NM_198903.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr5:161524717 C>T maps to NM_198903.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr6:2948609 G>A maps to ENST00000316782 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr6:2948609 G>A maps to ENST00000316782 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr6:41621180 C>T maps to NM_005586.3 C203C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr6:41621180 C>T maps to NM_005586.3 C203C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr6:85469989 C>G maps to NM_001080508.1 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr6:85469989 C>G maps to NM_001080508.1 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr7:4169595 G>A maps to NM_152744.3 G1332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr7:4169595 G>A maps to NM_152744.3 G1332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr7:26251376 G>C did not map to a codon.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr7:26251376 G>C did not map to a codon.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr7:117828388 C>T maps to NM_016200.4 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr7:117828388 C>T maps to NM_016200.4 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr7:154679392 G>A maps to NM_130797.2 A751A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr7:154679392 G>A maps to NM_130797.2 A751A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr8:105367307 C>T maps to NM_030788.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr8:105367307 C>T maps to NM_030788.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr8:113599422 G>A maps to NM_198123.1 L1253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr8:113599422 G>A maps to NM_198123.1 L1253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr8:116599314 A>C maps to NM_014112.2 A871A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr8:116599314 A>C maps to NM_014112.2 A871A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr8:124975614 C>T maps to NM_001039112.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr8:124975614 C>T maps to NM_001039112.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr8:145533468 G>A maps to NM_005526.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr8:145533468 G>A maps to NM_005526.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr9:121930222 G>A maps to NM_014618.2 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr9:121930222 G>A maps to NM_014618.2 I475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chrX:69649353 C>T maps to NM_001171192.1 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chrX:69649353 C>T maps to NM_001171192.1 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr1:43881681 G>A did not map to a codon.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr1:43881681 G>A did not map to a codon.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr1:44044586 G>A maps to NM_002840.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr1:44044586 G>A maps to NM_002840.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr1:156950258 G>A maps to NM_198236.1 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr1:156950258 G>A maps to NM_198236.1 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr1:160104994 C>T maps to NM_000702.3 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr1:160104994 C>T maps to NM_000702.3 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr1:201046134 G>C maps to NM_000069.2 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr1:201046134 G>C maps to NM_000069.2 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr1:203150382 G>A maps to NM_001276.2 Y206Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr1:203150382 G>A maps to NM_001276.2 Y206Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr1:240966239 G>A maps to ENST00000407727 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr1:240966239 G>A maps to ENST00000407727 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr10:95790918 C>G maps to ENST00000371380 S39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr10:95790918 C>G maps to ENST00000371380 S39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr11:4843391 C>A maps to NM_001004753.1 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr11:4843391 C>A maps to NM_001004753.1 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr11:118925376 G>A maps to NM_001130991.1 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr11:118925376 G>A maps to NM_001130991.1 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr12:6729532 C>T maps to ENST00000435659 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr12:6729532 C>T maps to ENST00000435659 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr12:11421067 G>A maps to NM_006249.4 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr12:11421067 G>A maps to NM_006249.4 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr12:130927170 G>A maps to NM_015347.4 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr12:130927170 G>A maps to NM_015347.4 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr14:67864497 G>A maps to NM_016445.1 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr14:67864497 G>A maps to NM_016445.1 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr16:20565100 A>C maps to NM_182617.3 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr16:20565100 A>C maps to NM_182617.3 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr16:23541091 G>A maps to NM_001083614.1 Y398Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr16:23541091 G>A maps to NM_001083614.1 Y398Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr16:50811825 C>A maps to ENST00000311559 S371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr16:50811825 C>A maps to ENST00000311559 S371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr16:57689387 G>A maps to NM_005682.5 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr16:57689387 G>A maps to NM_005682.5 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr19:22156524 G>A maps to NM_007153.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr19:22156524 G>A maps to NM_007153.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr19:40971541 G>A maps to NM_000713.2 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr19:40971541 G>A maps to NM_000713.2 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr2:141806555 A>G maps to NM_018557.2 D596D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr2:141806555 A>G maps to NM_018557.2 D596D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr2:149226534 A>G maps to ENST00000404807 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr2:149226534 A>G maps to ENST00000404807 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr2:161029175 A>G maps to NM_000888.3 H275H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr2:161029175 A>G maps to NM_000888.3 H275H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr3:126070937 G>C maps to NM_014079.3 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr3:126070937 G>C maps to NM_014079.3 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr5:140960399 G>C maps to ENST00000398557 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr5:140960399 G>C maps to ENST00000398557 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr6:152451871 G>A maps to NM_182961.2 V8712V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr6:152451871 G>A maps to NM_182961.2 V8712V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr8:104897723 A>G maps to NM_001100117.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr8:104897723 A>G maps to NM_001100117.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr9:32635463 C>T maps to NM_153809.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr9:32635463 C>T maps to NM_153809.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr9:90343232 C>T maps to NM_145918.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chr9:90343232 C>T maps to NM_145918.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chrX:155232634 C>A maps to NM_002186.2 C31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5559-01A-01D-1512-08 chrX:155232634 C>A maps to NM_002186.2 C31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:17275396 C>T maps to NM_014675.3 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:17275396 C>T maps to NM_014675.3 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:103474058 G>T maps to NM_080629.2 S560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:103474058 G>T maps to NM_080629.2 S560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:156243194 G>A maps to NM_015327.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:156243194 G>A maps to NM_015327.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:170965782 T>C maps to NM_001163629.1 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:170965782 T>C maps to NM_001163629.1 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:180959167 G>C maps to NM_005819.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:180959167 G>C maps to NM_005819.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:205306714 G>A maps to NM_018203.1 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:205306714 G>A maps to NM_018203.1 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:212120047 C>T did not map to a codon.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:212120047 C>T did not map to a codon.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:247769129 C>G maps to NM_001001914.1 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:247769129 C>G maps to NM_001001914.1 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:249107241 G>A maps to NM_030645.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr1:249107241 G>A maps to NM_030645.1 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr11:4945554 A>C maps to NM_001005237.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr11:4945554 A>C maps to NM_001005237.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr11:65425830 G>A maps to NM_021975.3 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr11:65425830 G>A maps to NM_021975.3 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr11:82878337 A>G maps to NM_015885.3 E663E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr11:82878337 A>G maps to NM_015885.3 E663E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr11:103870956 G>A maps to NM_025208.4 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr11:103870956 G>A maps to NM_025208.4 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr11:117387377 G>A maps to NM_020693.2 I589I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr11:117387377 G>A maps to NM_020693.2 I589I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr11:121000846 T>G maps to NM_005422.2 S956S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr11:121000846 T>G maps to NM_005422.2 S956S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr12:118650750 G>A maps to NM_016281.3 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr12:118650750 G>A maps to NM_016281.3 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr13:42293869 C>T maps to NM_015058.1 P991P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr13:42293869 C>T maps to NM_015058.1 P991P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr14:64494409 C>T maps to NM_182914.2 Q2205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr14:64494409 C>T maps to NM_182914.2 Q2205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr15:31294735 T>C maps to NM_002420.4 R1367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr15:31294735 T>C maps to NM_002420.4 R1367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr15:45434284 C>T maps to NM_175940.1 I599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr15:45434284 C>T maps to NM_175940.1 I599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr15:89173492 G>T maps to NM_022767.3 G316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr15:89173492 G>T maps to NM_022767.3 G316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr16:72143369 C>T maps to NM_014003.3 P1146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr16:72143369 C>T maps to NM_014003.3 P1146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr16:74455116 G>A maps to NM_001011880.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr16:74455116 G>A maps to NM_001011880.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr17:80156246 T>C maps to ENST00000445854 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr17:80156246 T>C maps to ENST00000445854 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr19:10434233 G>A maps to NM_133452.2 C272C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr19:10434233 G>A maps to NM_133452.2 C272C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr19:23544196 T>C maps to NM_003430.2 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr19:23544196 T>C maps to NM_003430.2 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr19:33699841 T>G maps to NM_019849.2 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr19:33699841 T>G maps to NM_019849.2 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr19:36335329 C>T maps to NM_004646.3 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr19:36335329 C>T maps to NM_004646.3 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr19:58988809 G>C maps to NM_017908.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr19:58988809 G>C maps to NM_017908.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr2:32927944 A>G maps to NM_017735.4 K397K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr2:32927944 A>G maps to NM_017735.4 K397K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr2:37455846 T>C maps to NM_005760.2 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr2:37455846 T>C maps to NM_005760.2 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr2:160053171 G>T maps to NM_033394.2 R1011R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr2:160053171 G>T maps to NM_033394.2 R1011R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr2:170428348 G>C maps to NM_024622.3 S64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr2:170428348 G>C maps to NM_024622.3 S64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr21:10933917 C>A maps to NM_199261.2 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr21:10933917 C>A maps to NM_199261.2 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr22:24224829 C>T maps to NM_030807.3 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr22:24224829 C>T maps to NM_030807.3 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr22:26159337 C>T maps to ENST00000407587 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr22:26159337 C>T maps to ENST00000407587 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr3:9798303 G>A maps to NM_016821.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr3:9798303 G>A maps to NM_016821.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr3:49064206 C>T maps to NM_000884.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr3:49064206 C>T maps to NM_000884.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr4:81123530 C>T maps to NM_001099403.1 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr4:81123530 C>T maps to NM_001099403.1 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr4:140811146 G>A maps to ENST00000509479 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr4:140811146 G>A maps to ENST00000509479 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr4:187004612 C>T maps to NM_003265.2 I591I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr4:187004612 C>T maps to NM_003265.2 I591I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr5:837491 T>C maps to NM_024786.2 K296K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr5:837491 T>C maps to NM_024786.2 K296K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr5:74865316 G>T maps to NM_016218.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr5:74865316 G>T maps to NM_016218.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr5:140574506 C>T maps to NM_018930.3 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr5:140574506 C>T maps to NM_018930.3 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr5:140580774 A>C maps to NM_018931.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr5:140580774 A>C maps to NM_018931.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr5:140719965 C>A maps to NM_018915.2 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr5:140719965 C>A maps to NM_018915.2 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr5:141059693 G>A maps to NM_022481.5 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr5:141059693 G>A maps to NM_022481.5 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr6:136597186 T>C maps to NM_014739.2 K492K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr6:136597186 T>C maps to NM_014739.2 K492K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr6:157522506 C>T maps to ENST00000367148 T1633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr6:157522506 C>T maps to ENST00000367148 T1633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr7:141955073 C>A maps to NM_001001317.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr7:141955073 C>A maps to NM_001001317.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr8:48697812 G>A maps to NM_006904.6 L3655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr8:48697812 G>A maps to NM_006904.6 L3655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr8:77764910 T>C maps to NM_024721.4 F1918F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr8:77764910 T>C maps to NM_024721.4 F1918F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr8:87414409 A>G maps to NM_007013.3 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr8:87414409 A>G maps to NM_007013.3 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr8:110416785 C>G maps to ENST00000426474 Y459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr8:110416785 C>G maps to ENST00000426474 Y459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr8:120596203 G>A maps to NM_006209.3 Q537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr8:120596203 G>A maps to NM_006209.3 Q537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr8:145698667 G>T maps to NM_145754.2 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr8:145698667 G>T maps to NM_145754.2 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr9:135546191 G>A maps to NM_012204.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chr9:135546191 G>A maps to NM_012204.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chrX:12701690 C>T maps to ENST00000429478 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chrX:12701690 C>T maps to ENST00000429478 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chrX:78216655 C>T maps to NM_198333.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6868-01B-12D-1912-08 chrX:78216655 C>T maps to NM_198333.1 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:1430869 G>A maps to NM_031921.4 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:1430869 G>A maps to NM_031921.4 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:12939514 G>T maps to ENST00000376192 C429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:12939514 G>T maps to ENST00000376192 C429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:26510928 C>T maps to ENST00000374253 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:26510928 C>T maps to ENST00000374253 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:31187157 G>A maps to NM_002379.3 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:31187157 G>A maps to NM_002379.3 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:52826197 G>A maps to NM_032449.2 H167H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:52826197 G>A maps to NM_032449.2 H167H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:78332058 A>T maps to NM_198549.2 K516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:78332058 A>T maps to NM_198549.2 K516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:93167772 C>A did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:93167772 C>A did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:107691138 A>G did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:107691138 A>G did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:151611498 G>T maps to ENST00000458013 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:151611498 G>T maps to ENST00000458013 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:159898078 G>A maps to NM_001135050.1 F1033F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:159898078 G>A maps to NM_001135050.1 F1033F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:170633412 C>A maps to NM_022716.2 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:170633412 C>A maps to NM_022716.2 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:175092650 T>A maps to NM_022093.1 A922A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:175092650 T>A maps to NM_022093.1 A922A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:200954075 G>C maps to NM_017596.2 P1238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:200954075 G>C maps to NM_017596.2 P1238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:207072724 C>A maps to NM_001185156.1 C36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:207072724 C>A maps to NM_001185156.1 C36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:216019334 A>T maps to ENST00000366943 L2962L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:216019334 A>T maps to ENST00000366943 L2962L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:248790415 G>C maps to NM_001001964.1 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr1:248790415 G>C maps to NM_001001964.1 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:13378323 G>A maps to NM_012247.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:13378323 G>A maps to NM_012247.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:16562731 G>A maps to NM_001010908.1 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:16562731 G>A maps to NM_001010908.1 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:52103622 G>A maps to ENST00000361543 H90H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:52103622 G>A maps to ENST00000361543 H90H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:68687990 C>G maps to NM_178011.3 Y439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:68687990 C>G maps to NM_178011.3 Y439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:91177810 G>A maps to NM_012420.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:91177810 G>A maps to NM_012420.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:95995800 G>T maps to ENST00000371380 E782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:95995800 G>T maps to ENST00000371380 E782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:98770784 G>C maps to NM_003061.2 V1102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:98770784 G>C maps to NM_003061.2 V1102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:105218106 G>A maps to NM_001001412.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:105218106 G>A maps to NM_001001412.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:117061410 G>T maps to NM_207303.2 L892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:117061410 G>T maps to NM_207303.2 L892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:124036331 C>A maps to ENST00000368994 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:124036331 C>A maps to ENST00000368994 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:124399935 G>C maps to ENST00000368915 T2441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:124399935 G>C maps to ENST00000368915 T2441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:126370313 C>A maps to NM_014661.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr10:126370313 C>A maps to NM_014661.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:6588903 C>T maps to NM_144666.2 A4055A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:6588903 C>T maps to NM_144666.2 A4055A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:16834668 C>A maps to ENST00000448080 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:16834668 C>A maps to ENST00000448080 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:18010156 C>G maps to NM_012139.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:18010156 C>G maps to NM_012139.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:48239278 A>T maps to NM_001005470.1 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:48239278 A>T maps to NM_001005470.1 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:56431877 C>A maps to NM_001004730.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:56431877 C>A maps to NM_001004730.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:57886520 A>G maps to NM_001005211.1 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:57886520 A>G maps to NM_001005211.1 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:92564959 T>A maps to ENST00000298047 S3218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:92564959 T>A maps to ENST00000298047 S3218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:99715884 C>A maps to NM_014361.2 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:99715884 C>A maps to NM_014361.2 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:124189697 G>T maps to NM_001002918.1 Y132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:124189697 G>T maps to NM_001002918.1 Y132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:128709439 T>A maps to NM_000220.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr11:128709439 T>A maps to NM_000220.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:6943183 G>T maps to NM_014262.3 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:6943183 G>T maps to NM_014262.3 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:7640426 T>G maps to NM_004244.4 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:7640426 T>G maps to NM_004244.4 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:15654947 C>G maps to NM_030667.1 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:15654947 C>G maps to NM_030667.1 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:20876189 T>G did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:20876189 T>G did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:39720118 T>C maps to ENST00000395670 V1116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:39720118 T>C maps to ENST00000395670 V1116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:40707844 G>C maps to NM_198578.3 S1536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:40707844 G>C maps to NM_198578.3 S1536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:52862854 G>A maps to NM_173086.4 Y562Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:52862854 G>A maps to NM_173086.4 Y562Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:56641849 G>A maps to NM_173595.3 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:56641849 G>A maps to NM_173595.3 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:65130828 T>C maps to ENST00000418919 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:65130828 T>C maps to ENST00000418919 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:81768457 A>T maps to NM_003625.2 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:81768457 A>T maps to NM_003625.2 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:100492320 T>C did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:100492320 T>C did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:106461452 G>T maps to NM_014840.2 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:106461452 G>T maps to NM_014840.2 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:112684765 G>C maps to NM_001109662.2 V1312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:112684765 G>C maps to NM_001109662.2 V1312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:113543581 G>A maps to NM_001193520.1 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:113543581 G>A maps to NM_001193520.1 F590F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:120947834 G>C maps to NM_032314.3 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr12:120947834 G>C maps to NM_032314.3 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr13:19751081 G>T maps to NM_006001.1 C347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr13:19751081 G>T maps to NM_006001.1 C347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr13:60590251 C>T maps to NM_001042517.1 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr13:60590251 C>T maps to NM_001042517.1 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr14:68274301 C>A maps to NM_015346.3 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr14:68274301 C>A maps to NM_015346.3 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr14:100172988 T>A maps to NM_006668.1 L150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr14:100172988 T>A maps to NM_006668.1 L150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr15:23890798 G>T maps to NM_019066.4 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr15:23890798 G>T maps to NM_019066.4 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr15:67757466 G>T maps to NM_001031715.2 V836V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr15:67757466 G>T maps to NM_001031715.2 V836V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr15:74178504 T>A maps to NM_153356.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr15:74178504 T>A maps to NM_153356.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr15:84657463 G>T maps to NM_207517.2 G1246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr15:84657463 G>T maps to NM_207517.2 G1246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr16:7629789 C>T maps to NM_145891.2 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr16:7629789 C>T maps to NM_145891.2 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr16:64984724 G>A maps to NM_001797.2 A613A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr16:64984724 G>A maps to NM_001797.2 A613A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr16:65022109 C>A maps to NM_001797.2 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr16:65022109 C>A maps to NM_001797.2 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr16:67981322 C>T maps to NM_005072.4 W661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr16:67981322 C>T maps to NM_005072.4 W661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:6913396 T>C maps to NM_000697.2 C588C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:6913396 T>C maps to NM_000697.2 C588C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:7317750 A>T maps to NM_020795.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:7317750 A>T maps to NM_020795.2 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:18638706 C>A maps to NM_001037330.1 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:18638706 C>A maps to NM_001037330.1 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:34074282 G>A maps to NM_139285.2 H279H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:34074282 G>A maps to NM_139285.2 H279H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:42475960 C>A maps to NM_001002909.2 E1162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:42475960 C>A maps to NM_001002909.2 E1162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:42852064 G>T did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:42852064 G>T did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:56247543 C>T maps to NM_001004707.3 N176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:56247543 C>T maps to NM_001004707.3 N176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:59489602 C>T maps to NM_203425.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:59489602 C>T maps to NM_203425.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:72588217 A>T maps to NM_152460.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr17:72588217 A>T maps to NM_152460.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr18:31224902 C>T maps to NM_030632.1 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr18:31224902 C>T maps to NM_030632.1 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr18:43316444 T>C maps to NM_001146037.1 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr18:43316444 T>C maps to NM_001146037.1 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr18:44555172 G>A maps to NM_145653.3 N347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr18:44555172 G>A maps to NM_145653.3 N347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr18:47806251 C>T did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr18:47806251 C>T did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:852882 G>A maps to NM_001972.2 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:852882 G>A maps to NM_001972.2 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:9075388 G>A maps to NM_024690.2 D4019D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:9075388 G>A maps to NM_024690.2 D4019D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:10893765 C>T maps to NM_001005361.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:10893765 C>T maps to NM_001005361.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:13869956 G>T maps to NM_030818.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:13869956 G>T maps to NM_030818.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:21205624 A>T maps to NM_025189.3 K12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:21205624 A>T maps to NM_025189.3 K12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:22363717 G>A maps to NM_001001411.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:22363717 G>A maps to NM_001001411.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:35617861 G>A maps to NM_139284.2 Q230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:35617861 G>A maps to NM_139284.2 Q230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:37488354 G>T maps to ENST00000455427 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:37488354 G>T maps to ENST00000455427 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:40317963 C>A maps to NM_004714.1 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:40317963 C>A maps to NM_004714.1 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:47422367 G>T maps to NM_004491.4 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:47422367 G>T maps to NM_004491.4 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:52272135 G>C maps to NM_001005738.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr19:52272135 G>C maps to NM_001005738.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:10923307 G>A maps to NM_001039362.1 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:10923307 G>A maps to NM_001039362.1 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:51254949 G>A maps to ENST00000404971 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:51254949 G>A maps to ENST00000404971 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:68521023 C>A maps to NM_015463.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:68521023 C>A maps to NM_015463.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:80529963 C>T maps to NM_178839.4 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:80529963 C>T maps to NM_178839.4 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:88405917 G>C maps to NM_198274.3 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:88405917 G>C maps to NM_198274.3 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:98999859 C>T maps to NM_001298.2 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:98999859 C>T maps to NM_001298.2 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:99439550 G>T maps to NM_207362.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:99439550 G>T maps to NM_207362.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:108626896 T>A maps to NM_021815.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:108626896 T>A maps to NM_021815.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:202900650 G>A maps to NM_003507.1 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:202900650 G>A maps to NM_003507.1 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:230652348 G>A maps to ENST00000389044 Q1596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:230652348 G>A maps to ENST00000389044 Q1596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:242741243 C>T maps to NM_022134.2 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr2:242741243 C>T maps to NM_022134.2 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr20:9561115 G>T maps to NM_177990.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr20:9561115 G>T maps to NM_177990.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr20:31877738 G>T maps to NM_033197.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr20:31877738 G>T maps to NM_033197.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr20:60581805 T>C maps to NM_003185.3 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr20:60581805 T>C maps to NM_003185.3 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr20:62597873 G>A maps to NM_020713.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr20:62597873 G>A maps to NM_020713.1 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr21:36042976 G>C maps to ENST00000360731 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr21:36042976 G>C maps to ENST00000360731 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr22:23465616 G>A maps to NM_002073.2 *356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr22:23465616 G>A maps to NM_002073.2 *356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr22:24622661 C>G maps to NM_001099781.1 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr22:24622661 C>G maps to NM_001099781.1 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr22:29835040 G>A maps to NM_021026.2 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr22:29835040 G>A maps to NM_021026.2 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr22:31059930 G>C maps to NM_152511.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr22:31059930 G>C maps to NM_152511.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr3:109047836 T>A maps to NM_018189.3 K260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr3:109047836 T>A maps to NM_018189.3 K260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr3:122662293 G>T maps to NM_001031702.2 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr3:122662293 G>T maps to NM_001031702.2 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr3:123333077 G>A maps to NM_053025.3 C1873C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr3:123333077 G>A maps to NM_053025.3 C1873C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr3:130293226 G>A maps to NM_001102608.1 V1135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr3:130293226 G>A maps to NM_001102608.1 V1135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr3:154802865 C>G maps to NM_007289.2 S60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr3:154802865 C>G maps to NM_007289.2 S60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr3:170843829 C>A maps to NM_015028.2 V628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr3:170843829 C>A maps to NM_015028.2 V628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr3:185161245 C>T maps to NM_004721.3 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr3:185161245 C>T maps to NM_004721.3 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:3516630 T>A maps to NM_002337.2 K287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:3516630 T>A maps to NM_002337.2 K287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:10444811 G>A maps to NM_053042.2 D1047D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:10444811 G>A maps to NM_053042.2 D1047D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:57190343 A>G maps to NM_020722.1 P1151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:57190343 A>G maps to NM_020722.1 P1151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:68919653 A>G maps to NM_207407.2 D430D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:68919653 A>G maps to NM_207407.2 D430D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:69978303 C>A maps to NM_001074.2 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:69978303 C>A maps to NM_001074.2 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:72629168 G>C maps to ENST00000504199 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:72629168 G>C maps to ENST00000504199 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:129770158 C>T maps to NM_199320.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:129770158 C>T maps to NM_199320.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:142053644 G>T maps to NM_020724.1 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:142053644 G>T maps to NM_020724.1 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:169305795 G>T maps to NM_001012967.1 S1361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr4:169305795 G>T maps to NM_001012967.1 S1361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:39306835 G>C maps to NM_001737.3 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:39306835 G>C maps to NM_001737.3 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:41160244 G>T maps to NM_001115131.1 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:41160244 G>T maps to NM_001115131.1 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:45262355 G>C maps to NM_021072.2 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:45262355 G>C maps to NM_021072.2 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:45396680 G>T maps to NM_021072.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:45396680 G>T maps to NM_021072.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:70798482 A>G maps to NM_018429.2 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:70798482 A>G maps to NM_018429.2 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:89986665 G>A maps to NM_032119.3 K2253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:89986665 G>A maps to NM_032119.3 K2253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:93076444 C>T maps to NM_153216.1 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:93076444 C>T maps to NM_153216.1 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:135379744 A>G did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:135379744 A>G did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:140188124 C>T maps to NM_018907.2 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:140188124 C>T maps to NM_018907.2 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:140256338 C>A maps to NM_018903.2 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:140256338 C>A maps to NM_018903.2 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:176637519 C>G maps to NM_022455.4 S707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr5:176637519 C>G maps to NM_022455.4 S707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr6:25830750 C>T did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr6:25830750 C>T did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr6:26197202 C>A maps to NM_003530.3 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr6:26197202 C>A maps to NM_003530.3 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr6:27835169 C>T maps to NM_005322.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr6:27835169 C>T maps to NM_005322.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr6:69666696 C>A maps to NM_001704.2 C507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr6:69666696 C>A maps to NM_001704.2 C507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr6:132859538 C>T maps to NM_175057.3 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr6:132859538 C>T maps to NM_175057.3 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr6:152605235 C>G maps to NM_182961.2 L6028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr6:152605235 C>G maps to NM_182961.2 L6028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:48285512 C>A maps to NM_152701.3 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:48285512 C>A maps to NM_152701.3 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:90419959 C>T maps to NM_012395.2 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:90419959 C>T maps to NM_012395.2 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:94740689 G>T maps to NM_001166160.1 V505V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:94740689 G>T maps to NM_001166160.1 V505V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:105111199 C>A maps to NM_019042.3 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:105111199 C>A maps to NM_019042.3 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:117432537 G>T maps to NM_033427.2 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:117432537 G>T maps to NM_033427.2 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:143141255 C>A maps to NM_177437.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:143141255 C>A maps to NM_177437.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:150644573 G>A maps to NM_000238.2 F998F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:150644573 G>A maps to NM_000238.2 F998F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:155255139 G>T maps to NM_001427.3 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr7:155255139 G>T maps to NM_001427.3 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr8:2820915 G>T maps to NM_033225.5 A3094A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr8:2820915 G>T maps to NM_033225.5 A3094A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr8:52287227 A>G maps to NM_144651.4 P1207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr8:52287227 A>G maps to NM_144651.4 P1207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr8:104898350 C>T maps to NM_001100117.2 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr8:104898350 C>T maps to NM_001100117.2 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr8:113267586 G>T maps to NM_198123.1 S3311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr8:113267586 G>T maps to NM_198123.1 S3311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr8:117954795 G>A did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr8:117954795 G>A did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr8:124978245 G>A did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr8:124978245 G>A did not map to a codon.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr8:139263090 A>G maps to NM_015912.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr8:139263090 A>G maps to NM_015912.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:35556329 G>A maps to NM_001135999.1 L956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:35556329 G>A maps to NM_001135999.1 L956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:90502038 C>T maps to NM_178828.4 A879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:90502038 C>T maps to NM_178828.4 A879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:99694505 G>A maps to NM_001170741.1 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:99694505 G>A maps to NM_001170741.1 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:109691070 A>G maps to NM_021224.4 E1626E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:109691070 A>G maps to NM_021224.4 E1626E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:112898558 T>G maps to NM_007203.4 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:112898558 T>G maps to NM_007203.4 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:112899251 G>T maps to NM_007203.4 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:112899251 G>T maps to NM_007203.4 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:119202970 C>A maps to ENST00000313400 L1233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:119202970 C>A maps to ENST00000313400 L1233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:120470942 C>T maps to NM_138554.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chr9:120470942 C>T maps to NM_138554.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chrX:17739578 G>T maps to NM_198270.2 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chrX:17739578 G>T maps to NM_198270.2 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chrX:34962222 G>T maps to NM_152631.2 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chrX:34962222 G>T maps to NM_152631.2 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chrX:153693210 G>A maps to NM_017514.3 E681E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6869-01A-11D-1870-08 chrX:153693210 G>A maps to NM_017514.3 E681E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr1:40703346 A>G maps to NM_012421.3 K991K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr1:40703346 A>G maps to NM_012421.3 K991K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr1:156618414 G>A maps to NM_021948.3 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr1:156618414 G>A maps to NM_021948.3 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr1:229773395 C>A maps to NM_014777.2 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr1:229773395 C>A maps to NM_014777.2 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr1:247695696 C>G maps to NM_198074.4 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr1:247695696 C>G maps to NM_198074.4 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr11:66617873 G>A maps to NM_022172.2 Y845Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr11:66617873 G>A maps to NM_022172.2 Y845Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr12:3935379 G>A maps to NM_020367.4 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr12:3935379 G>A maps to NM_020367.4 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr12:7864204 G>T maps to NM_199286.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr12:7864204 G>T maps to NM_199286.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr12:49434543 G>A maps to NM_003482.3 Q2337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr12:49434543 G>A maps to NM_003482.3 Q2337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr12:54936369 G>A maps to NM_005337.4 E1095E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr12:54936369 G>A maps to NM_005337.4 E1095E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr12:130847536 G>A maps to NM_004764.4 A681A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr12:130847536 G>A maps to NM_004764.4 A681A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr13:32936726 A>T maps to NM_000059.3 R2625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr13:32936726 A>T maps to NM_000059.3 R2625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr14:65239588 G>A maps to ENST00000389723 I1758I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr14:65239588 G>A maps to ENST00000389723 I1758I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr16:23570828 C>T maps to ENST00000219638 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr16:23570828 C>T maps to ENST00000219638 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr16:72110553 C>T maps to ENST00000228226 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr16:72110553 C>T maps to ENST00000228226 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr17:10584495 C>T maps to NM_004589.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr17:10584495 C>T maps to NM_004589.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr19:4418036 A>G maps to NM_005483.2 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr19:4418036 A>G maps to NM_005483.2 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr19:21606459 C>T maps to NM_001076678.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr19:21606459 C>T maps to NM_001076678.2 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr2:190532560 G>A maps to NM_019048.2 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr2:190532560 G>A maps to NM_019048.2 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr20:10653369 C>G maps to NM_000214.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr20:10653369 C>G maps to NM_000214.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr20:41101055 G>A maps to ENST00000373198 Q434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr20:41101055 G>A maps to ENST00000373198 Q434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr21:44153464 G>A did not map to a codon.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr21:44153464 G>A did not map to a codon.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr3:47450917 G>A maps to NM_015466.2 E603E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr3:47450917 G>A maps to NM_015466.2 E603E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr3:129695839 G>A maps to NM_007117.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr3:129695839 G>A maps to NM_007117.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr4:68606302 A>T maps to NM_000406.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr4:68606302 A>T maps to NM_000406.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr5:140202874 T>C maps to NM_018908.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr5:140202874 T>C maps to NM_018908.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr5:140588970 C>A maps to NM_018932.3 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr5:140588970 C>A maps to NM_018932.3 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr5:140755398 G>A maps to NM_018919.2 E583E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr5:140755398 G>A maps to NM_018919.2 E583E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr5:169506011 G>A maps to NM_004946.2 P1676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr5:169506011 G>A maps to NM_004946.2 P1676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr6:31605290 A>G maps to NM_080686.2 E2134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr6:31605290 A>G maps to NM_080686.2 E2134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr7:66453483 T>C maps to NM_016038.2 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr7:66453483 T>C maps to NM_016038.2 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr9:1057242 T>C maps to NM_181872.4 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chr9:1057242 T>C maps to NM_181872.4 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chrX:96213114 G>T maps to NM_006729.4 E635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chrX:96213114 G>T maps to NM_006729.4 E635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chrX:120182677 C>A maps to NM_012084.3 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chrX:120182677 C>A maps to NM_012084.3 I380I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chrX:153223610 A>T maps to ENST00000369984 P631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6870-01A-11D-1870-08 chrX:153223610 A>T maps to ENST00000369984 P631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr1:26658051 G>A maps to NM_001039775.3 G1414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr1:26658051 G>A maps to NM_001039775.3 G1414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr1:34666532 C>T maps to NM_001134734.1 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr1:34666532 C>T maps to NM_001134734.1 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr1:119474282 G>A maps to ENST00000369429 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr1:119474282 G>A maps to ENST00000369429 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr1:154987573 A>C maps to ENST00000417934 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr1:154987573 A>C maps to ENST00000417934 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr1:215824102 C>T maps to ENST00000366943 W4725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr1:215824102 C>T maps to ENST00000366943 W4725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr10:114044407 C>T maps to NM_058222.1 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr10:114044407 C>T maps to NM_058222.1 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr11:56230772 G>A maps to NM_001004743.1 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr11:56230772 G>A maps to NM_001004743.1 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr11:111571712 A>G maps to NM_015191.1 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr11:111571712 A>G maps to NM_015191.1 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr11:118260438 G>A did not map to a codon.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr11:118260438 G>A did not map to a codon.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr11:122724649 G>T did not map to a codon.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr11:122724649 G>T did not map to a codon.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr11:134095033 C>T maps to NM_052875.3 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr11:134095033 C>T maps to NM_052875.3 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr12:1250923 G>T maps to NM_178040.2 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr12:1250923 G>T maps to NM_178040.2 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr12:56743975 T>A did not map to a codon.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr12:56743975 T>A did not map to a codon.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr12:130921645 G>C maps to NM_015347.4 S599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr12:130921645 G>C maps to NM_015347.4 S599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr13:88330087 G>A maps to NM_015567.1 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr13:88330087 G>A maps to NM_015567.1 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr14:50092738 G>A maps to NM_018139.2 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr14:50092738 G>A maps to NM_018139.2 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr14:63860549 G>C maps to ENST00000422769 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr14:63860549 G>C maps to ENST00000422769 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr15:57815715 G>A maps to NM_032866.3 Q915Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr15:57815715 G>A maps to NM_032866.3 Q915Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr16:57149417 C>T maps to NM_152727.5 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr16:57149417 C>T maps to NM_152727.5 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr18:42530339 G>A maps to NM_015559.2 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr18:42530339 G>A maps to NM_015559.2 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr19:17942158 G>T maps to NM_000215.3 A952A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr19:17942158 G>T maps to NM_000215.3 A952A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr19:48800481 G>A maps to NM_144577.3 F588F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr19:48800481 G>A maps to NM_144577.3 F588F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr2:80085145 G>A maps to ENST00000402739 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr2:80085145 G>A maps to ENST00000402739 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr2:86716519 C>G maps to NM_001146688.1 V1131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr2:86716519 C>G maps to NM_001146688.1 V1131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr2:128394475 C>A maps to ENST00000389524 C2080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr2:128394475 C>A maps to ENST00000389524 C2080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr2:179439599 G>A maps to NM_133378.4 N21185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr2:179439599 G>A maps to NM_133378.4 N21185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr2:226447437 C>T maps to NM_020864.1 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr2:226447437 C>T maps to NM_020864.1 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr3:57658126 T>C maps to NM_152678.2 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr3:57658126 T>C maps to NM_152678.2 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr3:159997001 C>G maps to ENST00000483754 V776V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr3:159997001 C>G maps to ENST00000483754 V776V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr3:164905936 G>T maps to NM_014926.2 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr3:164905936 G>T maps to NM_014926.2 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr3:196530018 G>C maps to NM_002577.4 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr3:196530018 G>C maps to NM_002577.4 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr4:81122460 A>C maps to NM_001099403.1 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr4:81122460 A>C maps to NM_001099403.1 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr4:123270378 C>T maps to NM_015312.3 I4449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr4:123270378 C>T maps to NM_015312.3 I4449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr5:1253932 C>A maps to NM_198253.2 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr5:1253932 C>A maps to NM_198253.2 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr5:157166326 A>T did not map to a codon.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr5:157166326 A>T did not map to a codon.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr6:52847395 G>A maps to NM_001512.3 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr6:52847395 G>A maps to NM_001512.3 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr6:139495642 C>T maps to NM_016217.2 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr6:139495642 C>T maps to NM_016217.2 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr7:912966 G>A maps to ENST00000456758 *975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr7:912966 G>A maps to ENST00000456758 *975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr7:6043689 C>G did not map to a codon.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr7:6043689 C>G did not map to a codon.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr7:6731675 A>T maps to ENST00000330442 C356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr7:6731675 A>T maps to ENST00000330442 C356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr7:50450283 G>A maps to NM_006060.3 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr7:50450283 G>A maps to NM_006060.3 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr7:91695763 T>C maps to NM_005751.4 H2078H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr7:91695763 T>C maps to NM_005751.4 H2078H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr7:141797391 G>C did not map to a codon.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr7:141797391 G>C did not map to a codon.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr8:144947142 G>A maps to NM_031308.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr8:144947142 G>A maps to NM_031308.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr9:137715308 C>A maps to NM_000093.3 G1564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chr9:137715308 C>A maps to NM_000093.3 G1564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chrX:23700511 G>A did not map to a codon.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chrX:23700511 G>A did not map to a codon.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chrX:53631657 G>A maps to ENST00000276009 G878G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6871-01A-11D-1870-08 chrX:53631657 G>A maps to ENST00000276009 G878G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr1:82416119 A>T maps to ENST00000370717 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr1:82416119 A>T maps to ENST00000370717 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr1:160165805 G>A maps to NM_001231.4 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr1:160165805 G>A maps to NM_001231.4 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr10:73892813 C>G did not map to a codon.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr10:73892813 C>G did not map to a codon.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr10:82330000 C>T maps to NM_207372.2 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr10:82330000 C>T maps to NM_207372.2 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr10:98078207 C>A maps to NM_004088.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr10:98078207 C>A maps to NM_004088.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr10:108489806 C>T did not map to a codon.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr10:108489806 C>T did not map to a codon.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr11:16816212 G>C maps to ENST00000448080 S856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr11:16816212 G>C maps to ENST00000448080 S856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr11:92577878 C>T maps to ENST00000298047 N3782N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr11:92577878 C>T maps to ENST00000298047 N3782N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr11:121174254 C>G maps to NM_001024956.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr11:121174254 C>G maps to NM_001024956.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr12:121442192 C>T maps to NM_022895.1 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr12:121442192 C>T maps to NM_022895.1 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr12:125397264 T>C maps to NM_021009.5 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr12:125397264 T>C maps to NM_021009.5 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr14:74061757 A>G maps to NM_152331.3 K222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr14:74061757 A>G maps to NM_152331.3 K222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr15:81614832 G>A maps to NM_181900.2 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr15:81614832 G>A maps to NM_181900.2 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr16:20442540 G>A did not map to a codon.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr16:20442540 G>A did not map to a codon.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr17:6900304 G>A maps to NM_000697.2 W99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr17:6900304 G>A maps to NM_000697.2 W99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr17:72619722 G>C maps to ENST00000426295 S54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr17:72619722 G>C maps to ENST00000426295 S54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr18:33935605 C>T maps to NM_025135.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr18:33935605 C>T maps to NM_025135.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr19:2121202 G>A maps to ENST00000355272 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr19:2121202 G>A maps to ENST00000355272 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr19:2717765 G>A maps to NM_145173.3 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr19:2717765 G>A maps to NM_145173.3 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr19:21720753 T>C maps to NM_001001415.2 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr19:21720753 T>C maps to NM_001001415.2 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr19:36051331 G>A maps to NM_000704.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr19:36051331 G>A maps to NM_000704.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr19:59028614 C>T maps to NM_032792.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr19:59028614 C>T maps to NM_032792.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr2:149868126 G>A maps to NM_004522.1 T937T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr2:149868126 G>A maps to NM_004522.1 T937T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr2:166848066 G>A maps to NM_001165963.1 I1906I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr2:166848066 G>A maps to NM_001165963.1 I1906I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr2:168101808 G>T maps to NM_152381.5 E1303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr2:168101808 G>T maps to NM_152381.5 E1303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr20:35717459 C>T maps to NM_002895.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr20:35717459 C>T maps to NM_002895.2 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr21:46047690 C>G maps to NM_198690.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr21:46047690 C>G maps to NM_198690.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr22:18301235 C>T maps to NM_015241.2 E1397E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr22:18301235 C>T maps to NM_015241.2 E1397E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr22:24463126 C>T maps to NM_012295.3 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr22:24463126 C>T maps to NM_012295.3 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr22:26928675 C>T maps to NM_003595.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr22:26928675 C>T maps to NM_003595.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr3:36873987 G>C maps to NM_014831.2 L2318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr3:36873987 G>C maps to NM_014831.2 L2318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr3:124207130 C>T maps to NM_001024660.3 A1453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr3:124207130 C>T maps to NM_001024660.3 A1453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr4:72635072 G>A maps to ENST00000504199 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr4:72635072 G>A maps to ENST00000504199 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr5:140181795 C>G maps to NM_018906.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr5:140181795 C>G maps to NM_018906.2 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr5:169535530 T>A maps to NM_012188.4 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr5:169535530 T>A maps to NM_012188.4 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr6:57472426 G>T maps to NM_000947.2 G406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr6:57472426 G>T maps to NM_000947.2 G406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr6:85472389 C>G maps to NM_001080508.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr6:85472389 C>G maps to NM_001080508.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr7:121738532 G>A maps to NM_005763.3 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr7:121738532 G>A maps to NM_005763.3 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr8:77763746 G>C maps to NM_024721.4 T1530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr8:77763746 G>C maps to NM_024721.4 T1530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr8:113317028 A>G maps to NM_198123.1 Y2729Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr8:113317028 A>G maps to NM_198123.1 Y2729Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr9:21970970 G>T maps to NM_001195132.1 Y129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chr9:21970970 G>T maps to NM_001195132.1 Y129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chrX:151818952 C>T maps to NM_018558.2 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6872-01A-11D-1870-08 chrX:151818952 C>T maps to NM_018558.2 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr1:7902813 G>C maps to ENST00000377532 *1211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr1:7902813 G>C maps to ENST00000377532 *1211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr1:16462184 G>A maps to NM_004431.3 R465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr1:16462184 G>A maps to NM_004431.3 R465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr1:44069438 G>A maps to NM_002840.3 K872K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr1:44069438 G>A maps to NM_002840.3 K872K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr1:47691449 G>A maps to ENST00000371883 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr1:47691449 G>A maps to ENST00000371883 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr1:156845367 T>C maps to NM_002529.3 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr1:156845367 T>C maps to NM_002529.3 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr1:222721185 G>A maps to NM_024746.3 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr1:222721185 G>A maps to NM_024746.3 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr1:248402848 C>T maps to NM_017504.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr1:248402848 C>T maps to NM_017504.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr10:106907397 C>T maps to NM_014978.1 D442D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr10:106907397 C>T maps to NM_014978.1 D442D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr11:89395321 C>T did not map to a codon.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr11:89395321 C>T did not map to a codon.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr12:111895023 A>G maps to NM_002973.3 P1170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr12:111895023 A>G maps to NM_002973.3 P1170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr14:34269099 C>T maps to NM_001164749.1 D529D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr14:34269099 C>T maps to NM_001164749.1 D529D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr14:103357699 C>T maps to NM_145725.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr14:103357699 C>T maps to NM_145725.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr18:7926656 G>A maps to NM_001105244.1 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr18:7926656 G>A maps to NM_001105244.1 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr19:42754039 G>A maps to NM_006494.2 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr19:42754039 G>A maps to NM_006494.2 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr2:54120867 T>C maps to NM_014614.2 S1327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr2:54120867 T>C maps to NM_014614.2 S1327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr2:202131410 C>T maps to NM_001080125.1 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr2:202131410 C>T maps to NM_001080125.1 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr20:1161908 C>T maps to NM_018354.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr20:1161908 C>T maps to NM_018354.1 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr21:47409673 A>G maps to NM_001848.2 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr21:47409673 A>G maps to NM_001848.2 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr22:31979943 C>G maps to NM_001007467.1 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr22:31979943 C>G maps to NM_001007467.1 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr22:40669447 C>T maps to ENST00000454349 D1009D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr22:40669447 C>T maps to ENST00000454349 D1009D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr3:151082799 T>C maps to NM_053002.4 Y962Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr3:151082799 T>C maps to NM_053002.4 Y962Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr4:187539563 G>A maps to ENST00000260147 R2729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr4:187539563 G>A maps to ENST00000260147 R2729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr5:637679 C>G maps to NM_018140.3 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr5:637679 C>G maps to NM_018140.3 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr5:178369800 C>A maps to NM_182594.2 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr5:178369800 C>A maps to NM_182594.2 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr6:7230731 G>A maps to NM_001003699.3 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr6:7230731 G>A maps to NM_001003699.3 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-6873-01A-11D-1870-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr1:197072272 C>A maps to NM_018136.4 V2036V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr1:197072272 C>A maps to NM_018136.4 V2036V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr1:213436153 C>T maps to NM_012424.3 Q1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr1:213436153 C>T maps to NM_012424.3 Q1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr10:93038048 T>G maps to NM_032373.3 Y249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr10:93038048 T>G maps to NM_032373.3 Y249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr10:94294474 T>C maps to NM_004969.3 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr10:94294474 T>C maps to NM_004969.3 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr10:105218229 G>A maps to NM_001001412.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr10:105218229 G>A maps to NM_001001412.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr10:135053282 C>G maps to NM_014468.2 Y115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr10:135053282 C>G maps to NM_014468.2 Y115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr12:7065323 C>T maps to ENST00000416215 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr12:7065323 C>T maps to ENST00000416215 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr13:23942585 G>C maps to NM_014363.4 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr13:23942585 G>C maps to NM_014363.4 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr13:70549921 G>A maps to NM_020866.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr13:70549921 G>A maps to NM_020866.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr14:38724914 G>A maps to NM_175060.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr14:38724914 G>A maps to NM_175060.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr14:86088850 T>C maps to NM_013231.4 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr14:86088850 T>C maps to NM_013231.4 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr16:4774825 C>T maps to NM_133450.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr16:4774825 C>T maps to NM_133450.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr16:64984855 G>A maps to NM_001797.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr16:64984855 G>A maps to NM_001797.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr17:38450240 A>G maps to NM_001254.3 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr17:38450240 A>G maps to NM_001254.3 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr18:65180849 G>T maps to NM_032160.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr18:65180849 G>T maps to NM_032160.2 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr19:35175565 A>G maps to ENST00000221282 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr19:35175565 A>G maps to ENST00000221282 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr19:50463938 G>A maps to NM_052884.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr19:50463938 G>A maps to NM_052884.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr2:99160453 C>T maps to NM_001134224.1 D311D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr2:99160453 C>T maps to NM_001134224.1 D311D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr2:219510939 T>A maps to NM_001105537.1 K469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr2:219510939 T>A maps to NM_001105537.1 K469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr3:124906104 G>A maps to NM_001195483.1 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr3:124906104 G>A maps to NM_001195483.1 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr4:107016737 T>G maps to NM_001163436.1 A824A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr4:107016737 T>G maps to NM_001163436.1 A824A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr6:28540655 C>A maps to NM_052923.1 E1004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr6:28540655 C>A maps to NM_052923.1 E1004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr6:29429638 T>A maps to NM_030883.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr6:29429638 T>A maps to NM_030883.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr6:38690576 C>T did not map to a codon.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr6:38690576 C>T did not map to a codon.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr6:52268766 C>A maps to ENST00000361841 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr6:52268766 C>A maps to ENST00000361841 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr7:4249657 C>T maps to NM_152744.3 A1801A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr7:4249657 C>T maps to NM_152744.3 A1801A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr7:87910313 C>T maps to NM_024636.2 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr7:87910313 C>T maps to NM_024636.2 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr7:98608796 C>A maps to ENST00000359863 T3673T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr7:98608796 C>A maps to ENST00000359863 T3673T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr7:133979788 G>A maps to NM_032826.4 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr7:133979788 G>A maps to NM_032826.4 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr8:118847730 A>T maps to NM_000127.2 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr8:118847730 A>T maps to NM_000127.2 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr9:79117749 C>T maps to NM_001097636.1 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chr9:79117749 C>T maps to NM_001097636.1 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chrX:125685718 G>A maps to NM_178470.4 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chrX:125685718 G>A maps to NM_178470.4 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chrX:152113984 C>T maps to NM_001178106.1 V493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-7269-01A-11D-2012-08 chrX:152113984 C>T maps to NM_001178106.1 V493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr10:71003037 C>T maps to NM_025130.3 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr10:71003037 C>T maps to NM_025130.3 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr14:30100143 G>A maps to NM_002742.2 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr14:30100143 G>A maps to NM_002742.2 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr14:94956061 G>A maps to NM_173850.2 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr14:94956061 G>A maps to NM_173850.2 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr16:72159280 T>G maps to NM_031293.2 T759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr16:72159280 T>G maps to NM_031293.2 T759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr16:76556035 G>A maps to NM_033401.3 V878V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr16:76556035 G>A maps to NM_033401.3 V878V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr19:15587144 C>T maps to NM_052890.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr19:15587144 C>T maps to NM_052890.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr22:40059770 C>T maps to NM_021096.3 Y1174Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr22:40059770 C>T maps to NM_021096.3 Y1174Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr3:186760907 C>T maps to NM_003032.2 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr3:186760907 C>T maps to NM_003032.2 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr4:46307678 A>G maps to ENST00000507069 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr4:46307678 A>G maps to ENST00000507069 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr9:135277017 G>A maps to NM_007344.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4217-01A-11D-2078-08 chr9:135277017 G>A maps to NM_007344.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:10715870 C>T did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:10715870 C>T did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:11896102 C>T maps to ENST00000376496 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:11896102 C>T maps to ENST00000376496 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:29029012 C>G maps to NM_006582.2 S231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:29029012 C>G maps to NM_006582.2 S231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:62908867 G>A maps to NM_003368.4 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:62908867 G>A maps to NM_003368.4 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:70518707 G>C did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:70518707 G>C did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:160128898 C>G maps to NM_144699.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:160128898 C>G maps to NM_144699.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:171178064 C>G maps to NM_001460.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:171178064 C>G maps to NM_001460.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:211842542 G>A maps to NM_002497.2 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:211842542 G>A maps to NM_002497.2 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:229462742 C>A maps to NM_145257.3 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:229462742 C>A maps to NM_145257.3 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:248525532 G>A maps to NM_001004696.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:248525532 G>A maps to NM_001004696.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr10:33200865 G>A maps to ENST00000374956 F552F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr10:33200865 G>A maps to ENST00000374956 F552F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr10:135096617 G>A maps to NM_006659.2 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr10:135096617 G>A maps to NM_006659.2 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:621850 G>A maps to NM_021924.4 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:621850 G>A maps to NM_021924.4 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:3784170 G>C maps to NM_016320.4 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:3784170 G>C maps to NM_016320.4 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:5510655 T>C maps to NM_001005163.2 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:5510655 T>C maps to NM_001005163.2 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:6291977 C>T maps to NM_176875.2 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:6291977 C>T maps to NM_176875.2 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:6621415 G>C maps to NM_015324.2 S444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:6621415 G>C maps to NM_015324.2 S444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:27384411 C>T maps to NM_030771.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:27384411 C>T maps to NM_030771.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:50003784 G>A maps to NM_001005270.2 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:50003784 G>A maps to NM_001005270.2 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:65338883 C>G maps to NM_006396.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:65338883 C>G maps to NM_006396.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:65638807 C>A maps to NM_016938.3 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:65638807 C>A maps to NM_016938.3 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:66811230 C>T maps to NM_001177880.1 N248N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:66811230 C>T maps to NM_001177880.1 N248N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:67120196 C>T maps to NM_021173.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr11:67120196 C>T maps to NM_021173.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr12:8375317 G>A maps to NM_018088.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr12:8375317 G>A maps to NM_018088.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr12:49690817 G>A maps to ENST00000451891 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr12:49690817 G>A maps to ENST00000451891 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr12:63225905 C>T maps to NM_020700.1 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr12:63225905 C>T maps to NM_020700.1 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr12:108082472 C>T maps to NM_007062.1 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr12:108082472 C>T maps to NM_007062.1 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr12:108939001 G>C maps to NM_014706.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr12:108939001 G>C maps to NM_014706.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr15:31218128 C>T maps to NM_014967.4 S825S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr15:31218128 C>T maps to NM_014967.4 S825S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr15:41864734 C>T maps to NM_006293.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr15:41864734 C>T maps to NM_006293.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr15:56387890 G>A maps to NM_022841.5 Q679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr15:56387890 G>A maps to NM_022841.5 Q679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr15:90210856 C>T maps to NM_002666.4 E313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr15:90210856 C>T maps to NM_002666.4 E313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr16:30727496 C>G maps to NM_006662.2 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr16:30727496 C>G maps to NM_006662.2 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr16:69184785 C>T maps to NM_032830.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr16:69184785 C>T maps to NM_032830.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr16:75203688 C>T maps to NM_153688.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr16:75203688 C>T maps to NM_153688.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr16:75579248 C>T did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr16:75579248 C>T did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr16:81045654 G>A maps to NM_001100624.1 Q37Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr16:81045654 G>A maps to NM_001100624.1 Q37Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr16:84211374 C>G maps to NM_178452.4 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr16:84211374 C>G maps to NM_178452.4 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr17:7557556 C>G maps to NM_001678.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr17:7557556 C>G maps to NM_001678.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr17:46152375 C>G maps to ENST00000442683 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr17:46152375 C>G maps to ENST00000442683 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr18:580885 G>T maps to NM_004066.1 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr18:580885 G>T maps to NM_004066.1 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr18:3879504 G>A maps to NM_004746.2 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr18:3879504 G>A maps to NM_004746.2 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr18:72180809 G>A maps to NM_018235.2 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr18:72180809 G>A maps to NM_018235.2 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:2254198 C>T maps to NM_144616.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:2254198 C>T maps to NM_144616.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:6743835 C>T maps to ENST00000313244 Q211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:6743835 C>T maps to ENST00000313244 Q211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:10227614 C>T maps to NM_003755.3 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:10227614 C>T maps to NM_003755.3 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:19656684 C>T maps to NM_153221.2 R1111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:19656684 C>T maps to NM_153221.2 R1111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:35786780 C>G maps to NM_002361.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:35786780 C>G maps to NM_002361.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:36637119 C>A maps to NM_001749.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:36637119 C>A maps to NM_001749.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:46387754 C>T maps to NM_015649.1 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:46387754 C>T maps to NM_015649.1 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:51955700 G>A maps to NM_014442.2 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr19:51955700 G>A maps to NM_014442.2 R478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:1497616 G>A maps to NM_000547.5 E604E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:1497616 G>A maps to NM_000547.5 E604E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:24928093 C>T maps to NM_003743.4 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:24928093 C>T maps to NM_003743.4 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:73868551 G>A maps to NM_003960.3 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:73868551 G>A maps to NM_003960.3 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:105665723 G>A maps to NM_182640.2 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:105665723 G>A maps to NM_182640.2 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:113410355 C>T maps to NM_005415.3 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:113410355 C>T maps to NM_005415.3 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:128186311 G>A maps to ENST00000409048 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:128186311 G>A maps to ENST00000409048 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:130832365 G>A maps to NM_001099771.2 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:130832365 G>A maps to NM_001099771.2 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:135659428 G>C maps to NM_138326.2 *337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:135659428 G>C maps to NM_138326.2 *337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:161052753 G>A maps to NM_000888.3 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:161052753 G>A maps to NM_000888.3 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:179569096 C>G maps to NM_133378.4 L8756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:179569096 C>G maps to NM_133378.4 L8756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:227973310 G>A maps to ENST00000396625 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:227973310 G>A maps to ENST00000396625 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:232393431 G>A maps to NM_006056.4 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr2:232393431 G>A maps to NM_006056.4 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr20:2820549 G>A maps to NM_022760.3 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr20:2820549 G>A maps to NM_022760.3 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr20:20023026 C>T maps to NM_016652.4 W530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr20:20023026 C>T maps to NM_016652.4 W530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr20:45905247 C>T maps to ENST00000471951 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr20:45905247 C>T maps to ENST00000471951 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr20:56099081 G>A maps to ENST00000423479 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr20:56099081 G>A maps to ENST00000423479 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr21:34635243 G>T maps to NM_207585.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr21:34635243 G>T maps to NM_207585.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr22:26894917 G>A maps to NM_012143.2 I451I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr22:26894917 G>A maps to NM_012143.2 I451I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr22:26895393 G>A maps to NM_012143.2 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr22:26895393 G>A maps to NM_012143.2 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr22:38254698 G>C maps to ENST00000262832 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr22:38254698 G>C maps to ENST00000262832 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr22:50898406 G>C maps to ENST00000337034 V1165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr22:50898406 G>C maps to ENST00000337034 V1165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr3:38101287 G>A maps to NM_007335.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr3:38101287 G>A maps to NM_007335.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr3:48626387 G>A maps to NM_000094.3 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr3:48626387 G>A maps to NM_000094.3 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr3:49155174 G>C maps to ENST00000434032 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr3:49155174 G>C maps to ENST00000434032 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr3:51993285 G>C maps to NM_033010.2 S220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr3:51993285 G>C maps to NM_033010.2 S220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr4:514998 G>A maps to NM_001127178.1 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr4:514998 G>A maps to NM_001127178.1 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr4:41016053 G>A maps to NM_004307.1 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr4:41016053 G>A maps to NM_004307.1 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr4:95496978 C>T maps to NM_006457.3 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr4:95496978 C>T maps to NM_006457.3 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr4:158073942 G>T maps to NM_001166060.1 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr4:158073942 G>T maps to NM_001166060.1 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr4:184367347 C>T maps to NM_017632.2 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr4:184367347 C>T maps to NM_017632.2 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr5:137354084 G>A maps to NM_016603.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr5:137354084 G>A maps to NM_016603.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr5:140237153 G>T maps to NM_018901.2 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr5:140237153 G>T maps to NM_018901.2 V507V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr5:156522383 G>A maps to NM_032782.3 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr5:156522383 G>A maps to NM_032782.3 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:7572177 G>A maps to NM_004415.2 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:7572177 G>A maps to NM_004415.2 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:38950168 C>T maps to ENST00000327475 F4282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:38950168 C>T maps to ENST00000327475 F4282F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:43222388 C>T maps to NM_032538.1 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:43222388 C>T maps to NM_032538.1 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:44254174 C>G maps to NM_182539.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:44254174 C>G maps to NM_182539.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:56357811 G>A maps to ENST00000361203 Q6613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:56357811 G>A maps to ENST00000361203 Q6613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:56513370 C>G maps to ENST00000361203 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:56513370 C>G maps to ENST00000361203 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:73952216 G>A maps to ENST00000370385 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:73952216 G>A maps to ENST00000370385 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:100901695 G>C maps to ENST00000262901 S67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr6:100901695 G>C maps to ENST00000262901 S67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr7:2623916 G>A maps to NM_152558.3 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr7:2623916 G>A maps to NM_152558.3 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr7:19765223 G>T maps to NM_152774.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr7:19765223 G>T maps to NM_152774.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr7:55240702 G>A maps to NM_005228.3 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr7:55240702 G>A maps to NM_005228.3 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr7:77006224 C>G did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr7:77006224 C>G did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr7:100365620 C>G maps to ENST00000349350 L1676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr7:100365620 C>G maps to ENST00000349350 L1676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr7:137363311 G>C maps to NM_004717.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr7:137363311 G>C maps to NM_004717.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr7:148702239 G>A maps to NM_004911.4 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr7:148702239 G>A maps to NM_004911.4 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr8:19316070 G>A maps to NM_018371.4 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr8:19316070 G>A maps to NM_018371.4 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr8:74922332 C>T maps to NM_015364.4 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr8:74922332 C>T maps to NM_015364.4 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr8:94934632 C>T maps to NM_001161778.1 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr8:94934632 C>T maps to NM_001161778.1 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:5920394 G>A maps to NM_001017969.2 F1867F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:5920394 G>A maps to NM_001017969.2 F1867F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:19316772 C>G maps to NM_017925.4 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:19316772 C>G maps to NM_017925.4 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:20820387 C>G maps to NM_017794.3 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:20820387 C>G maps to NM_017794.3 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:21481363 G>A maps to NM_176891.4 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:21481363 G>A maps to NM_176891.4 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:87325653 G>A maps to NM_006180.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:87325653 G>A maps to NM_006180.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:130687444 G>A maps to NM_001135219.1 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:130687444 G>A maps to NM_001135219.1 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:130687477 G>C maps to NM_001135219.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:130687477 G>C maps to NM_001135219.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:135357755 G>A maps to NM_207417.1 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr9:135357755 G>A maps to NM_207417.1 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chrX:138698571 G>A maps to ENST00000370578 Q499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chrX:138698571 G>A maps to ENST00000370578 Q499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr1:36904425 G>A maps to ENST00000356637 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr1:36904425 G>A maps to ENST00000356637 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr11:294140 C>T maps to ENST00000409479 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr11:294140 C>T maps to ENST00000409479 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr11:988625 A>T maps to ENST00000332231 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr11:988625 A>T maps to ENST00000332231 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr11:62457909 G>A maps to NM_001130702.1 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr11:62457909 G>A maps to NM_001130702.1 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr11:114314648 C>T maps to NM_015523.3 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr11:114314648 C>T maps to NM_015523.3 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr12:11138841 G>C maps to NM_176890.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr12:11138841 G>C maps to NM_176890.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr12:14976228 G>A maps to NM_175874.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr12:14976228 G>A maps to NM_175874.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr12:44177512 G>T maps to NM_016123.3 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr12:44177512 G>T maps to NM_016123.3 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr12:111744813 C>T maps to NM_015267.3 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr12:111744813 C>T maps to NM_015267.3 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr13:58208359 C>T maps to NM_001040429.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr13:58208359 C>T maps to NM_001040429.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr15:45981252 C>G maps to NM_021199.2 S378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr15:45981252 C>G maps to NM_021199.2 S378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr16:24988543 T>G maps to NM_001006634.1 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr16:24988543 T>G maps to NM_001006634.1 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr16:30736321 C>T maps to NM_006662.2 S1859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr16:30736321 C>T maps to NM_006662.2 S1859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr16:77465452 G>A maps to NM_199355.2 H78H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr16:77465452 G>A maps to NM_199355.2 H78H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr17:7256192 G>A did not map to a codon.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr17:7256192 G>A did not map to a codon.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr17:7578499 G>A maps to NM_001126112.1 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr17:7578499 G>A maps to NM_001126112.1 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr19:14001122 C>T maps to ENST00000454313 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr19:14001122 C>T maps to ENST00000454313 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr3:41275253 C>T maps to NM_001904.3 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr3:41275253 C>T maps to NM_001904.3 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr4:6711284 G>A maps to NM_203462.2 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr4:6711284 G>A maps to NM_203462.2 F24F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr4:156825276 T>C did not map to a codon.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr4:156825276 T>C did not map to a codon.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr6:47254184 G>T maps to NM_014452.3 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr6:47254184 G>T maps to NM_014452.3 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr7:22534407 C>A maps to ENST00000441815 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr7:22534407 C>A maps to ENST00000441815 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr7:48411939 C>G maps to NM_152701.3 S3660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr7:48411939 C>G maps to NM_152701.3 S3660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr7:107224423 C>T maps to NM_001008405.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr7:107224423 C>T maps to NM_001008405.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr8:131862049 C>T did not map to a codon.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr8:131862049 C>T did not map to a codon.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr9:140332686 C>T maps to NM_001033113.1 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4224-01A-01D-1434-08 chr9:140332686 C>T maps to NM_001033113.1 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr1:110882128 C>T maps to NM_022768.4 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr1:110882128 C>T maps to NM_022768.4 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr1:233270851 C>T maps to NM_014801.3 L1248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr1:233270851 C>T maps to NM_014801.3 L1248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr10:116057014 G>A maps to NM_001001936.1 T757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr10:116057014 G>A maps to NM_001001936.1 T757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr11:17426126 G>A maps to ENST00000302539 F1164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr11:17426126 G>A maps to ENST00000302539 F1164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr11:62159698 C>T maps to NM_025080.3 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr11:62159698 C>T maps to NM_025080.3 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr11:64033384 G>A maps to NM_000932.2 T1021T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr11:64033384 G>A maps to NM_000932.2 T1021T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr11:70260655 C>T maps to NM_001184740.1 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr11:70260655 C>T maps to NM_001184740.1 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr11:72292992 T>C did not map to a codon.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr11:72292992 T>C did not map to a codon.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr11:111916645 C>T maps to NM_001931.4 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr11:111916645 C>T maps to NM_001931.4 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr12:12315146 G>A maps to NM_002336.2 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr12:12315146 G>A maps to NM_002336.2 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr12:101480442 C>T maps to ENST00000392977 C514C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr12:101480442 C>T maps to ENST00000392977 C514C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr15:89450551 G>A maps to NM_005928.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr15:89450551 G>A maps to NM_005928.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr16:4947768 C>T maps to NM_002705.4 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr16:4947768 C>T maps to NM_002705.4 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr17:2604100 G>A maps to NM_015229.3 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr17:2604100 G>A maps to NM_015229.3 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr17:19835243 C>T maps to NM_007202.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr17:19835243 C>T maps to NM_007202.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr17:26851657 C>T maps to NM_003593.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr17:26851657 C>T maps to NM_003593.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr17:36491541 G>A maps to ENST00000398597 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr17:36491541 G>A maps to ENST00000398597 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr17:39122693 G>A maps to NM_213656.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr17:39122693 G>A maps to NM_213656.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr17:67186543 C>A maps to NM_080282.3 E696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr17:67186543 C>A maps to NM_080282.3 E696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr18:76753934 G>A maps to NM_171999.2 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr18:76753934 G>A maps to NM_171999.2 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr19:10202782 G>A maps to NM_018381.2 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr19:10202782 G>A maps to NM_018381.2 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr2:111666364 G>A did not map to a codon.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr2:111666364 G>A did not map to a codon.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr2:177033994 A>C maps to NM_006898.4 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr2:177033994 A>C maps to NM_006898.4 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr20:35827571 C>T maps to NM_002951.3 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr20:35827571 C>T maps to NM_002951.3 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr3:129251102 C>T maps to NM_000539.3 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr3:129251102 C>T maps to NM_000539.3 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr3:196288328 C>T maps to NM_182627.1 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr3:196288328 C>T maps to NM_182627.1 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr5:140248819 C>T maps to NM_018902.3 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr5:140248819 C>T maps to NM_018902.3 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr5:140731947 C>T maps to NM_018922.2 I707I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr5:140731947 C>T maps to NM_018922.2 I707I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr6:143825111 G>A maps to NM_032020.4 D230D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr6:143825111 G>A maps to NM_032020.4 D230D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr6:145069595 G>A maps to NM_007124.2 K2718K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr6:145069595 G>A maps to NM_007124.2 K2718K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr7:5521495 G>A maps to NM_024963.4 D689D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr7:5521495 G>A maps to NM_024963.4 D689D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr7:87027900 C>T maps to NM_001143935.1 Q622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr7:87027900 C>T maps to NM_001143935.1 Q622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr7:127231135 C>T maps to NM_001662.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr7:127231135 C>T maps to NM_001662.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr8:25159857 C>T maps to NM_024940.6 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr8:25159857 C>T maps to NM_024940.6 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr9:113168735 G>A maps to ENST00000374463 A3051A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr9:113168735 G>A maps to ENST00000374463 A3051A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr9:138516491 C>T maps to NM_182974.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4225-01A-01D-1434-08 chr9:138516491 C>T maps to NM_182974.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:2160774 C>T maps to NM_003036.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:2160774 C>T maps to NM_003036.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:33236756 C>G maps to NM_020888.2 V659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:33236756 C>G maps to NM_020888.2 V659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:40627250 G>A maps to NM_012421.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:40627250 G>A maps to NM_012421.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:115275261 G>C maps to NM_001130523.1 S353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:115275261 G>C maps to NM_001130523.1 S353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:118165573 C>A maps to NM_017709.3 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:118165573 C>A maps to NM_017709.3 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:120165543 G>A maps to NM_001080470.1 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:120165543 G>A maps to NM_001080470.1 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:150972983 G>C maps to NM_001163258.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:150972983 G>C maps to NM_001163258.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:152327319 G>C maps to NM_001014342.2 S981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:152327319 G>C maps to NM_001014342.2 S981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:155002951 C>G maps to NM_144622.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:155002951 C>G maps to NM_144622.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:158735617 G>A maps to NM_001005185.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:158735617 G>A maps to NM_001005185.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:168281972 C>T maps to NM_005149.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:168281972 C>T maps to NM_005149.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:179095630 G>A maps to NM_007314.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:179095630 G>A maps to NM_007314.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:203144776 G>C maps to NM_004997.2 S36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:203144776 G>C maps to NM_004997.2 S36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:247978845 C>T maps to NM_001001966.1 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr1:247978845 C>T maps to NM_001001966.1 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr10:12070766 G>C maps to NM_015542.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr10:12070766 G>C maps to NM_015542.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr10:17737123 C>T maps to NM_003473.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr10:17737123 C>T maps to NM_003473.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr10:61822995 C>T maps to NM_020987.2 S4156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr10:61822995 C>T maps to NM_020987.2 S4156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr10:69881285 G>T maps to NM_032578.2 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr10:69881285 G>T maps to NM_032578.2 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr10:76928340 A>G maps to ENST00000372690 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr10:76928340 A>G maps to ENST00000372690 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr11:6191433 G>A maps to NM_001004052.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr11:6191433 G>A maps to NM_001004052.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr11:12248644 C>G maps to NM_014632.2 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr11:12248644 C>G maps to NM_014632.2 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr11:33182906 G>C did not map to a codon.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr11:33182906 G>C did not map to a codon.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr11:46341830 C>G maps to ENST00000288400 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr11:46341830 C>G maps to ENST00000288400 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr11:64507520 G>T maps to ENST00000320253 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr11:64507520 G>T maps to ENST00000320253 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr11:64534667 T>C maps to NM_201995.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr11:64534667 T>C maps to NM_201995.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr11:128844700 C>T maps to NM_001142685.1 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr11:128844700 C>T maps to NM_001142685.1 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr12:13221563 C>T maps to NM_020853.1 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr12:13221563 C>T maps to NM_020853.1 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr12:75601538 G>A maps to NM_139137.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr12:75601538 G>A maps to NM_139137.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr12:117217095 C>T maps to NM_001109903.1 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr12:117217095 C>T maps to NM_001109903.1 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr12:133350894 C>T maps to NM_005895.3 P1385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr12:133350894 C>T maps to NM_005895.3 P1385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr14:24617532 G>T maps to NM_017999.4 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr14:24617532 G>T maps to NM_017999.4 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr14:47426687 G>A maps to NM_001113498.2 Q660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr14:47426687 G>A maps to NM_001113498.2 Q660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr14:81610640 C>T maps to NM_000369.2 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr14:81610640 C>T maps to NM_000369.2 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr14:89039314 G>A maps to NM_024824.4 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr14:89039314 G>A maps to NM_024824.4 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr15:42743328 G>A maps to NM_022473.1 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr15:42743328 G>A maps to NM_022473.1 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr16:312519 C>G maps to NM_032039.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr16:312519 C>G maps to NM_032039.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr16:1961638 G>A maps to ENST00000454677 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr16:1961638 G>A maps to ENST00000454677 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr16:3071625 C>T maps to NM_016639.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr16:3071625 C>T maps to NM_016639.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr16:9857425 G>A maps to NM_000833.3 Y1325Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr16:9857425 G>A maps to NM_000833.3 Y1325Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr16:30005772 G>A maps to NM_003609.3 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr16:30005772 G>A maps to NM_003609.3 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr16:67405000 G>A maps to NM_018296.5 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr16:67405000 G>A maps to NM_018296.5 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:3101342 C>T maps to NM_012352.1 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:3101342 C>T maps to NM_012352.1 F177F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:7623113 G>A maps to NM_020877.2 W21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:7623113 G>A maps to NM_020877.2 W21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:26897882 C>T maps to NM_033198.3 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:26897882 C>T maps to NM_033198.3 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:37564042 C>T maps to NM_004774.3 Q1477Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:37564042 C>T maps to NM_004774.3 Q1477Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:38935780 C>T maps to NM_181537.3 E315E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:38935780 C>T maps to NM_181537.3 E315E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:73227441 C>T maps to NM_024844.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr17:73227441 C>T maps to NM_024844.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr18:77960665 G>A maps to NM_032510.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr18:77960665 G>A maps to NM_032510.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:1055345 C>T maps to NM_019112.3 Q1401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:1055345 C>T maps to NM_019112.3 Q1401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:17487788 C>G maps to NM_031310.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:17487788 C>G maps to NM_031310.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:19356216 C>T maps to NM_004386.2 N1196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:19356216 C>T maps to NM_004386.2 N1196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:39898585 C>T maps to NM_003407.2 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:39898585 C>T maps to NM_003407.2 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:45783692 G>A maps to NM_031417.3 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:45783692 G>A maps to NM_031417.3 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:47884110 C>G maps to NM_014681.5 V1007V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:47884110 C>G maps to NM_014681.5 V1007V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:51379883 C>G maps to NM_005551.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:51379883 C>G maps to NM_005551.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:52659058 G>C maps to NM_001102657.1 S626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr19:52659058 G>C maps to NM_001102657.1 S626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:38893362 G>A maps to NM_138801.2 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:38893362 G>A maps to NM_138801.2 E20E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:62067352 G>A maps to ENST00000404929 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:62067352 G>A maps to ENST00000404929 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:105912814 G>A maps to NM_004257.4 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:105912814 G>A maps to NM_004257.4 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:109103016 G>A maps to NM_181453.3 L1281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:109103016 G>A maps to NM_181453.3 L1281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:113780313 G>C maps to NM_014438.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:113780313 G>C maps to NM_014438.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:143797995 G>A did not map to a codon.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:143797995 G>A did not map to a codon.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:173429335 C>G maps to ENST00000392571 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:173429335 C>G maps to ENST00000392571 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:191362378 C>G maps to NM_017694.3 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr2:191362378 C>G maps to NM_017694.3 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr20:35173440 G>T maps to NM_006097.3 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr20:35173440 G>T maps to NM_006097.3 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr20:35444080 C>T maps to NM_080627.2 K588K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr20:35444080 C>T maps to NM_080627.2 K588K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr21:35467895 C>G maps to NM_006933.4 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr21:35467895 C>G maps to NM_006933.4 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr21:43531074 C>T maps to NM_173568.3 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr21:43531074 C>T maps to NM_173568.3 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr22:24483644 G>A maps to NM_012295.3 L1168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr22:24483644 G>A maps to NM_012295.3 L1168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr22:37637673 G>A maps to NM_002872.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr22:37637673 G>A maps to NM_002872.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr22:50854546 G>A maps to ENST00000216061 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr22:50854546 G>A maps to ENST00000216061 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:12777057 C>A maps to ENST00000431022 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:12777057 C>A maps to ENST00000431022 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:13670671 G>T maps to NM_001165035.1 E908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:13670671 G>T maps to NM_001165035.1 E908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:46759218 C>G maps to NM_013270.4 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:46759218 C>G maps to NM_013270.4 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:57743443 C>T maps to ENST00000428312 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:57743443 C>T maps to ENST00000428312 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:98518386 G>A maps to ENST00000326857 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:98518386 G>A maps to ENST00000326857 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:122474118 C>G maps to NM_024610.4 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:122474118 C>G maps to NM_024610.4 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:126219701 G>A maps to NM_001165974.1 H387H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:126219701 G>A maps to NM_001165974.1 H387H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:141161523 C>G maps to NM_001080412.2 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:141161523 C>G maps to NM_001080412.2 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:151072984 C>G maps to NM_053002.4 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:151072984 C>G maps to NM_053002.4 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:151078366 C>T maps to NM_053002.4 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:151078366 C>T maps to NM_053002.4 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:151155346 C>G maps to NM_178822.4 L2334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:151155346 C>G maps to NM_178822.4 L2334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:172070741 G>A maps to NM_022763.3 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:172070741 G>A maps to NM_022763.3 L888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:183493895 C>T maps to NM_018023.4 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:183493895 C>T maps to NM_018023.4 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:184298533 C>T maps to NM_004443.3 I802I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:184298533 C>T maps to NM_004443.3 I802I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:184298945 C>T maps to NM_004443.3 Q909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr3:184298945 C>T maps to NM_004443.3 Q909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr4:25671433 C>T maps to NM_006424.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr4:25671433 C>T maps to NM_006424.2 I267I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr4:39929691 G>A maps to NM_001100399.1 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr4:39929691 G>A maps to NM_001100399.1 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr4:40356014 G>C maps to NM_017581.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr4:40356014 G>C maps to NM_017581.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr4:71835699 C>T maps to ENST00000396051 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr4:71835699 C>T maps to ENST00000396051 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr5:41904483 C>G maps to NM_175921.4 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr5:41904483 C>G maps to NM_175921.4 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr6:30624383 G>C maps to NM_003587.4 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr6:30624383 G>C maps to NM_003587.4 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr6:34835328 G>A maps to NM_017754.3 E1218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr6:34835328 G>A maps to NM_017754.3 E1218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr6:35773512 G>A maps to NM_182548.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr6:35773512 G>A maps to NM_182548.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr6:43307215 G>C maps to NM_014345.2 S1507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr6:43307215 G>C maps to NM_014345.2 S1507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr6:53138059 A>G maps to ENST00000370918 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr6:53138059 A>G maps to ENST00000370918 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr6:54792427 C>A maps to NM_001010872.1 Y244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr6:54792427 C>A maps to NM_001010872.1 Y244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr7:552063 C>G maps to NM_002607.5 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr7:552063 C>G maps to NM_002607.5 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr7:70227854 G>T did not map to a codon.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr7:70227854 G>T did not map to a codon.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr7:98988656 G>A maps to NM_005720.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr7:98988656 G>A maps to NM_005720.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr7:100679094 G>C maps to NM_001040105.1 P1466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr7:100679094 G>C maps to NM_001040105.1 P1466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr7:107601752 C>T maps to NM_002291.2 P669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr7:107601752 C>T maps to NM_002291.2 P669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr7:158823438 C>G maps to ENST00000402066 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr7:158823438 C>G maps to ENST00000402066 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr8:41545689 G>C maps to ENST00000415018 L1414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr8:41545689 G>C maps to ENST00000415018 L1414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr8:59522252 T>C maps to NM_001144772.1 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr8:59522252 T>C maps to NM_001144772.1 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr8:68208740 G>A maps to NM_006421.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr8:68208740 G>A maps to NM_006421.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr8:95653587 C>T maps to NM_017697.3 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr8:95653587 C>T maps to NM_017697.3 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr8:107782022 C>T maps to NM_139166.4 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr8:107782022 C>T maps to NM_139166.4 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr8:110980589 G>A maps to NM_014379.2 F410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr8:110980589 G>A maps to NM_014379.2 F410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr8:144902848 G>C maps to NM_078480.1 S112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr8:144902848 G>C maps to NM_078480.1 S112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr9:87636300 C>G maps to NM_006180.3 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr9:87636300 C>G maps to NM_006180.3 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr9:125391589 T>G maps to NM_001004450.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr9:125391589 T>G maps to NM_001004450.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr9:140114908 C>T maps to NM_031297.3 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr9:140114908 C>T maps to NM_031297.3 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chrX:299608 C>G maps to NM_013239.4 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chrX:299608 C>G maps to NM_013239.4 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr14:103363705 C>T maps to NM_145725.2 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr14:103363705 C>T maps to NM_145725.2 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr15:41102894 C>T maps to NM_001077268.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr15:41102894 C>T maps to NM_001077268.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr15:43641113 C>T maps to ENST00000422466 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr15:43641113 C>T maps to ENST00000422466 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr16:30522384 C>G maps to NM_002209.2 S905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr16:30522384 C>G maps to NM_002209.2 S905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr16:30525151 C>T maps to NM_002209.2 V949V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr16:30525151 C>T maps to NM_002209.2 V949V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr19:3054132 C>T maps to NM_198969.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr19:3054132 C>T maps to NM_198969.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr19:6309769 G>A maps to NM_133492.2 N142N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr19:6309769 G>A maps to NM_133492.2 N142N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr19:46289910 C>T maps to NM_004943.1 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr19:46289910 C>T maps to NM_004943.1 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr2:189854842 C>T maps to NM_000090.3 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr2:189854842 C>T maps to NM_000090.3 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr22:29747174 G>A maps to NM_001127.3 C380C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr22:29747174 G>A maps to NM_001127.3 C380C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr4:126372964 A>G maps to NM_024582.4 G3598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr4:126372964 A>G maps to NM_024582.4 G3598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr6:37140829 G>A maps to ENST00000373507 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr6:37140829 G>A maps to ENST00000373507 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr6:127796905 G>A maps to NM_001012279.2 S755S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr6:127796905 G>A maps to NM_001012279.2 S755S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr8:3245094 C>T maps to NM_033225.5 P901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4228-01A-01D-1434-08 chr8:3245094 C>T maps to NM_033225.5 P901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7861-01A-11D-2229-08 chr1:1390874 C>T maps to NM_001039211.2 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7861-01A-11D-2229-08 chr1:1390874 C>T maps to NM_001039211.2 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7861-01A-11D-2229-08 chr1:1565046 C>T maps to NM_080875.2 I979I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7861-01A-11D-2229-08 chr1:1565046 C>T maps to NM_080875.2 I979I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7861-01A-11D-2229-08 chr1:3418444 G>A maps to ENST00000452816 S818S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7861-01A-11D-2229-08 chr1:3418444 G>A maps to ENST00000452816 S818S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7861-01A-11D-2229-08 chr11:74058231 G>A maps to NM_173582.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7861-01A-11D-2229-08 chr11:74058231 G>A maps to NM_173582.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7861-01A-11D-2229-08 chr17:7139303 G>A maps to NM_024297.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7861-01A-11D-2229-08 chr17:7139303 G>A maps to NM_024297.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7861-01A-11D-2229-08 chr19:41382567 G>A maps to NM_000764.2 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7861-01A-11D-2229-08 chr19:41382567 G>A maps to NM_000764.2 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7861-01A-11D-2229-08 chrX:89177311 C>G maps to NM_138960.3 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7861-01A-11D-2229-08 chrX:89177311 C>G maps to NM_138960.3 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:11294217 G>A maps to NM_004958.3 Y771Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:11294217 G>A maps to NM_004958.3 Y771Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:34066576 G>T maps to ENST00000373381 G2208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:34066576 G>T maps to ENST00000373381 G2208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:47282726 C>T maps to NM_001099772.1 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:47282726 C>T maps to NM_001099772.1 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:66062269 C>A maps to NM_002303.5 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:66062269 C>A maps to NM_002303.5 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:75805304 C>T maps to NM_152697.4 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:75805304 C>T maps to NM_152697.4 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:86200452 T>C maps to NM_152890.5 K1659K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:86200452 T>C maps to NM_152890.5 K1659K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:103381185 C>G did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:103381185 C>G did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:156500966 C>A maps to NM_178229.4 S1392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:156500966 C>A maps to NM_178229.4 S1392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:168007625 C>T maps to ENST00000367840 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:168007625 C>T maps to ENST00000367840 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:169391452 C>T maps to ENST00000367806 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:169391452 C>T maps to ENST00000367806 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:181767768 G>A maps to ENST00000357570 E2247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:181767768 G>A maps to ENST00000357570 E2247E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:207649643 C>T maps to NM_001006658.2 R928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:207649643 C>T maps to NM_001006658.2 R928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:237617717 G>T maps to NM_001035.2 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:237617717 G>T maps to NM_001035.2 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:240656337 G>T maps to NM_022469.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:240656337 G>T maps to NM_022469.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr10:26849702 G>A maps to NM_019043.3 K433K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr10:26849702 G>A maps to NM_019043.3 K433K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr10:50690804 C>A maps to NM_000124.2 T699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr10:50690804 C>A maps to NM_000124.2 T699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr10:78669855 T>C did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr10:78669855 T>C did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr10:97987323 T>G did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr10:97987323 T>G did not map to a codon.
Alternatively spliced codon TCGA-BB-7862-01A-21D-2229-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-BB-7862-01A-21D-2229-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr10:129347782 G>T maps to NM_001030013.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr10:129347782 G>T maps to NM_001030013.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:15098957 C>A maps to NM_000728.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:15098957 C>A maps to NM_000728.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:15098969 C>G maps to NM_000728.3 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:15098969 C>G maps to NM_000728.3 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:30354490 A>T maps to NM_152316.1 K169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:30354490 A>T maps to NM_152316.1 K169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:55340088 G>T maps to NM_001004701.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:55340088 G>T maps to NM_001004701.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:55904597 G>T maps to NM_001004064.1 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:55904597 G>T maps to NM_001004064.1 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:56128007 G>T maps to NM_001005205.1 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:56128007 G>T maps to NM_001005205.1 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:60971080 C>T maps to NM_001079807.1 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:60971080 C>T maps to NM_001079807.1 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:61032010 C>A maps to NM_152718.2 R726R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:61032010 C>A maps to NM_152718.2 R726R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:67803772 C>T maps to NM_002496.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:67803772 C>T maps to NM_002496.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:69063225 T>A maps to NM_138768.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:69063225 T>A maps to NM_138768.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:71932329 G>A maps to NM_001113536.1 W150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:71932329 G>A maps to NM_001113536.1 W150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:75139658 T>G maps to NM_001039548.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:75139658 T>G maps to NM_001039548.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:104869610 C>T did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:104869610 C>T did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:117403129 C>A maps to NM_020693.2 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:117403129 C>A maps to NM_020693.2 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:118513087 C>T maps to NM_015157.2 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:118513087 C>T maps to NM_015157.2 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:123756045 G>A maps to NM_001013743.1 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr11:123756045 G>A maps to NM_001013743.1 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr12:11461214 G>C maps to NM_002723.3 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr12:11461214 G>C maps to NM_002723.3 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr12:52159507 G>A maps to NM_014191.2 K866K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr12:52159507 G>A maps to NM_014191.2 K866K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr12:54396286 G>A maps to NM_006897.1 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr12:54396286 G>A maps to NM_006897.1 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr12:55367304 T>C did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr12:55367304 T>C did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr12:57870383 C>T maps to ENST00000393797 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr12:57870383 C>T maps to ENST00000393797 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr13:25825792 T>C maps to NM_004685.3 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr13:25825792 T>C maps to NM_004685.3 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr13:38320427 G>T maps to NM_003306.1 C181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr13:38320427 G>T maps to NM_003306.1 C181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr13:42891736 A>G maps to NM_016248.2 L1826L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr13:42891736 A>G maps to NM_016248.2 L1826L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr13:107145597 C>T maps to NM_004093.2 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr13:107145597 C>T maps to NM_004093.2 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr14:21487853 G>A maps to NM_201537.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr14:21487853 G>A maps to NM_201537.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr14:60592507 A>T maps to ENST00000404681 P1078P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr14:60592507 A>T maps to ENST00000404681 P1078P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr14:88658718 G>T maps to NM_138318.2 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr14:88658718 G>T maps to NM_138318.2 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr14:94754645 T>A maps to NM_001100607.1 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr14:94754645 T>A maps to NM_001100607.1 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr15:23812140 G>A maps to NM_005664.3 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr15:23812140 G>A maps to NM_005664.3 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr15:33926902 G>A maps to NM_001036.3 G1048G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr15:33926902 G>A maps to NM_001036.3 G1048G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr15:49254846 G>A maps to NM_203349.3 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr15:49254846 G>A maps to NM_203349.3 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr15:55933314 G>A maps to NM_173814.4 C711C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr15:55933314 G>A maps to NM_173814.4 C711C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr15:59553687 T>C maps to NM_004998.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr15:59553687 T>C maps to NM_004998.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr16:1544452 C>T maps to NM_016111.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr16:1544452 C>T maps to NM_016111.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr16:7568150 T>C maps to NM_145891.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr16:7568150 T>C maps to NM_145891.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr16:19883696 G>T maps to NM_016235.1 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr16:19883696 G>T maps to NM_016235.1 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr16:20497918 C>A maps to NM_001010845.2 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr16:20497918 C>A maps to NM_001010845.2 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr16:72108243 C>G maps to ENST00000228226 Y88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr16:72108243 C>G maps to ENST00000228226 Y88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr17:40914627 C>T maps to ENST00000456272 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr17:40914627 C>T maps to ENST00000456272 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr17:45906031 C>A maps to NM_145255.3 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr17:45906031 C>A maps to NM_145255.3 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr17:46669597 A>T maps to NM_002147.3 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr17:46669597 A>T maps to NM_002147.3 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr17:73815858 C>T maps to NM_001080419.1 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr17:73815858 C>T maps to NM_001080419.1 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr18:334985 C>T maps to NM_130386.2 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr18:334985 C>T maps to NM_130386.2 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr18:2938025 T>A maps to NM_014646.2 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr18:2938025 T>A maps to NM_014646.2 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr18:8819103 C>A maps to ENST00000456698 I1320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr18:8819103 C>A maps to ENST00000456698 I1320I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr18:13087591 A>G maps to NM_032142.3 L1980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr18:13087591 A>G maps to NM_032142.3 L1980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr18:48510847 C>G maps to NM_018696.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr18:48510847 C>G maps to NM_018696.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:1800000 C>A maps to NM_138813.2 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:1800000 C>A maps to NM_138813.2 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:9002555 G>A maps to NM_024690.2 H13420H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:9002555 G>A maps to NM_024690.2 H13420H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:9060523 G>A maps to NM_024690.2 T8974T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:9060523 G>A maps to NM_024690.2 T8974T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:11624044 T>C maps to NM_016581.3 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:11624044 T>C maps to NM_016581.3 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:12800868 C>T maps to ENST00000380339 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:12800868 C>T maps to ENST00000380339 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:19606651 G>C maps to ENST00000404158 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:19606651 G>C maps to ENST00000404158 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:35940897 C>A maps to NM_005306.2 Y94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:35940897 C>A maps to NM_005306.2 Y94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:38189042 A>G maps to NM_032689.4 H663H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:38189042 A>G maps to NM_032689.4 H663H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:42181429 A>T maps to NM_006890.3 Y236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:42181429 A>T maps to NM_006890.3 Y236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:45790801 C>T maps to NM_031417.3 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:45790801 C>T maps to NM_031417.3 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:55363639 C>A maps to NM_006737.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr19:55363639 C>A maps to NM_006737.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:11728899 G>C maps to NM_014668.3 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:11728899 G>C maps to NM_014668.3 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:29296560 G>T maps to NM_001029883.1 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:29296560 G>T maps to NM_001029883.1 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:71797012 C>A maps to NM_001130987.1 T976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:71797012 C>A maps to NM_001130987.1 T976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:80801321 C>A maps to ENST00000402739 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:80801321 C>A maps to ENST00000402739 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:158617404 C>T maps to NM_001111067.2 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:158617404 C>T maps to NM_001111067.2 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:167330397 G>C maps to NM_002976.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:167330397 G>C maps to NM_002976.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:179497259 G>A maps to NM_133378.4 I11923I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:179497259 G>A maps to NM_133378.4 I11923I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:206659495 G>A maps to NM_201266.1 W837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:206659495 G>A maps to NM_201266.1 W837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:220079137 T>A maps to NM_005689.2 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:220079137 T>A maps to NM_005689.2 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:223464698 G>T maps to NM_005687.3 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr2:223464698 G>T maps to NM_005687.3 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr20:9434013 G>A maps to NM_001172646.1 K967K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr20:9434013 G>A maps to NM_001172646.1 K967K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr20:44641954 C>A maps to NM_004994.2 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr20:44641954 C>A maps to NM_004994.2 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr20:50346509 C>A maps to NM_006045.1 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr20:50346509 C>A maps to NM_006045.1 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:108635028 C>G maps to NM_005459.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:108635028 C>G maps to NM_005459.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:109023500 C>A maps to NM_138815.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:109023500 C>A maps to NM_138815.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:115805399 G>A maps to NM_002338.3 C53C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:115805399 G>A maps to NM_002338.3 C53C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:140178480 C>G maps to NM_022131.2 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:140178480 C>G maps to NM_022131.2 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:151046054 G>A maps to NM_176894.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:151046054 G>A maps to NM_176894.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:180630487 G>T maps to NM_005087.3 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:180630487 G>T maps to NM_005087.3 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:194062678 G>A maps to NM_001080513.2 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:194062678 G>A maps to NM_001080513.2 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:194080602 G>T maps to NM_001135057.2 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr3:194080602 G>T maps to NM_001135057.2 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:680329 G>A maps to ENST00000404286 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:680329 G>A maps to ENST00000404286 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:3419260 C>T maps to NM_198229.2 H918H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:3419260 C>T maps to NM_198229.2 H918H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:38829446 C>A maps to NM_006068.3 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:38829446 C>A maps to NM_006068.3 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:69095161 G>T maps to NM_182502.3 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:69095161 G>T maps to NM_182502.3 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:114275821 A>G maps to NM_001148.4 A2016A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:114275821 A>G maps to NM_001148.4 A2016A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:122828720 A>T maps to NM_001130698.1 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:122828720 A>T maps to NM_001130698.1 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:126237811 C>T maps to NM_024582.4 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:126237811 C>T maps to NM_024582.4 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:151682969 T>G maps to NM_006726.3 A1870A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr4:151682969 T>G maps to NM_006726.3 A1870A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:1880912 C>G maps to NM_016358.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:1880912 C>G maps to NM_016358.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:3599604 G>C maps to NM_024337.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:3599604 G>C maps to NM_024337.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:34035785 G>T maps to NM_181435.4 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:34035785 G>T maps to NM_181435.4 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:38448427 G>A maps to ENST00000354891 P838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:38448427 G>A maps to ENST00000354891 P838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:55192205 C>T maps to NM_139017.4 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:55192205 C>T maps to NM_139017.4 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:137727660 G>A maps to NM_016604.3 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:137727660 G>A maps to NM_016604.3 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:140080471 C>G maps to NM_144723.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:140080471 C>G maps to NM_144723.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:140754339 A>G maps to NM_018919.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:140754339 A>G maps to NM_018919.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:145610480 G>A did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:145610480 G>A did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:156723751 C>A maps to ENST00000442283 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:156723751 C>A maps to ENST00000442283 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:159781810 C>A maps to NM_031908.4 G115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr5:159781810 C>A maps to NM_031908.4 G115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:7609063 G>A maps to NM_152551.3 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:7609063 G>A maps to NM_152551.3 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:30166631 C>T maps to NM_003449.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:30166631 C>T maps to NM_003449.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:30861115 C>G maps to NM_013994.2 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:30861115 C>G maps to NM_013994.2 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:38863889 G>A maps to ENST00000327475 A2931A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:38863889 G>A maps to ENST00000327475 A2931A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:50696656 G>A maps to NM_172238.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:50696656 G>A maps to NM_172238.3 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:51893045 C>G maps to NM_138694.3 S1156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:51893045 C>G maps to NM_138694.3 S1156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:80202313 T>G maps to NM_181714.3 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:80202313 T>G maps to NM_181714.3 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:131520610 T>C maps to ENST00000431975 N194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:131520610 T>C maps to ENST00000431975 N194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:165792846 C>T maps to NM_001130690.1 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr6:165792846 C>T maps to NM_001130690.1 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr7:11450925 C>A maps to ENST00000423059 E1236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr7:11450925 C>A maps to ENST00000423059 E1236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr7:21654859 G>A maps to NM_003777.3 K1327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr7:21654859 G>A maps to NM_003777.3 K1327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr7:57529303 C>T maps to NM_001159279.1 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr7:57529303 C>T maps to NM_001159279.1 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr7:72717962 T>A maps to NM_148956.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr7:72717962 T>A maps to NM_148956.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr7:156450871 C>T maps to NM_001184997.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr7:156450871 C>T maps to NM_001184997.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr8:37756683 C>T maps to NM_001002814.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr8:37756683 C>T maps to NM_001002814.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr8:114186128 A>G maps to NM_198123.1 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr8:114186128 A>G maps to NM_198123.1 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr9:113168501 C>T maps to ENST00000374463 P3129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr9:113168501 C>T maps to ENST00000374463 P3129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chrX:37028612 G>C maps to NM_001013736.2 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chrX:37028612 G>C maps to NM_001013736.2 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chrX:41026733 G>A did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chrX:41026733 G>A did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chrX:74289142 T>A maps to NM_004299.3 V505V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chrX:74289142 T>A maps to NM_004299.3 V505V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chrX:86919783 C>A maps to NM_057162.2 S649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chrX:86919783 C>A maps to NM_057162.2 S649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chrX:136649542 G>T maps to NM_003413.3 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chrX:136649542 G>T maps to NM_003413.3 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chrX:150869333 C>A maps to NM_024082.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chrX:150869333 C>A maps to NM_024082.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr1:11883822 G>A maps to ENST00000376496 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr1:11883822 G>A maps to ENST00000376496 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr1:36644167 G>A maps to NM_018067.3 Q619Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr1:36644167 G>A maps to NM_018067.3 Q619Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr1:87170605 G>T maps to ENST00000482504 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr1:87170605 G>T maps to ENST00000482504 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr1:212583848 C>T maps to NM_001198862.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr1:212583848 C>T maps to NM_001198862.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr10:15590479 G>A maps to NM_003638.1 R952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr10:15590479 G>A maps to NM_003638.1 R952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr11:92532046 G>A maps to ENST00000298047 K1956K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr11:92532046 G>A maps to ENST00000298047 K1956K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr12:46233254 C>T maps to NM_152641.2 Q492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr12:46233254 C>T maps to NM_152641.2 Q492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr14:24976686 G>A maps to NM_001836.2 C28C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr14:24976686 G>A maps to NM_001836.2 C28C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr15:74241807 G>A maps to NM_005576.2 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr15:74241807 G>A maps to NM_005576.2 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr16:8862754 G>A maps to NM_001127448.1 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr16:8862754 G>A maps to NM_001127448.1 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr16:67572622 G>A maps to NM_001193523.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr16:67572622 G>A maps to NM_001193523.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr16:89169064 C>T maps to NM_174917.2 H240H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr16:89169064 C>T maps to NM_174917.2 H240H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr18:61027013 C>A maps to NM_002035.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr18:61027013 C>A maps to NM_002035.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr19:6696607 G>A maps to NM_000064.2 G953G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr19:6696607 G>A maps to NM_000064.2 G953G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr19:7184412 C>T maps to NM_000208.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr19:7184412 C>T maps to NM_000208.2 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr19:11319682 G>A maps to ENST00000319867 A1616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr19:11319682 G>A maps to ENST00000319867 A1616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr19:16025590 G>A maps to NM_021187.3 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr19:16025590 G>A maps to NM_021187.3 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr19:51633176 C>T maps to NM_014441.2 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr19:51633176 C>T maps to NM_014441.2 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr2:239186553 C>A maps to NM_022817.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr2:239186553 C>A maps to NM_022817.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr20:32378905 C>T maps to ENST00000375200 C716C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr20:32378905 C>T maps to ENST00000375200 C716C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BB-7863-01A-11D-2229-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BB-7863-01A-11D-2229-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr22:24463008 C>G maps to NM_012295.3 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr22:24463008 C>G maps to NM_012295.3 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr22:50943407 C>T maps to NM_033200.2 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr22:50943407 C>T maps to NM_033200.2 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr3:16264171 C>T maps to NM_054110.4 H560H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr3:16264171 C>T maps to NM_054110.4 H560H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr3:122634456 C>T maps to NM_001031702.2 V606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr3:122634456 C>T maps to NM_001031702.2 V606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr4:30725116 G>A maps to NM_001173523.1 T691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr4:30725116 G>A maps to NM_001173523.1 T691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr6:29430085 A>G maps to NM_030883.3 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr6:29430085 A>G maps to NM_030883.3 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr6:34506203 G>A maps to NM_012391.1 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr6:34506203 G>A maps to NM_012391.1 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr7:51203859 C>A maps to ENST00000395542 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr7:51203859 C>A maps to ENST00000395542 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr7:120906435 C>T maps to NM_024913.4 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr7:120906435 C>T maps to NM_024913.4 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr8:55372476 C>T maps to NM_022454.3 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr8:55372476 C>T maps to NM_022454.3 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr8:101589288 C>G maps to NM_152628.3 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chr8:101589288 C>G maps to NM_152628.3 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chrX:153695913 C>T maps to NM_017514.3 A1156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7863-01A-11D-2229-08 chrX:153695913 C>T maps to NM_017514.3 A1156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr1:15793936 C>T maps to ENST00000375924 H269H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr1:15793936 C>T maps to ENST00000375924 H269H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr1:217856682 A>G maps to NM_138796.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr1:217856682 A>G maps to NM_138796.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr11:34182506 G>A maps to NM_145804.2 N780N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr11:34182506 G>A maps to NM_145804.2 N780N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr11:46741249 A>G did not map to a codon.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr11:46741249 A>G did not map to a codon.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr11:64695278 A>T maps to NM_006244.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr11:64695278 A>T maps to NM_006244.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr13:36402441 G>T maps to NM_004734.4 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr13:36402441 G>T maps to NM_004734.4 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr13:37011962 C>T maps to NM_003914.3 D165D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr13:37011962 C>T maps to NM_003914.3 D165D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr15:78390832 G>A maps to NM_001101404.1 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr15:78390832 G>A maps to NM_001101404.1 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr16:47733261 G>A maps to NM_000293.2 P1089P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr16:47733261 G>A maps to NM_000293.2 P1089P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr16:83711943 C>T maps to ENST00000268613 N472N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr16:83711943 C>T maps to ENST00000268613 N472N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr19:40319074 C>A maps to NM_004714.1 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr19:40319074 C>A maps to NM_004714.1 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr19:51518154 C>G maps to NM_001077500.1 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr19:51518154 C>G maps to NM_001077500.1 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr19:57647236 G>A maps to NM_052882.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr19:57647236 G>A maps to NM_052882.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr2:88828763 C>T maps to NM_152670.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr2:88828763 C>T maps to NM_152670.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr2:141032096 G>C maps to NM_018557.2 V4346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr2:141032096 G>C maps to NM_018557.2 V4346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr2:192818508 T>C maps to NM_016192.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr2:192818508 T>C maps to NM_016192.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr20:61982207 G>A maps to NM_000744.5 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr20:61982207 G>A maps to NM_000744.5 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr3:4687339 C>T maps to ENST00000356617 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr3:4687339 C>T maps to ENST00000356617 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr3:17255707 T>C maps to NM_001134381.1 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr3:17255707 T>C maps to NM_001134381.1 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr4:89039300 G>A maps to NM_004827.2 H267H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr4:89039300 G>A maps to NM_004827.2 H267H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr6:31939880 C>T maps to NM_032454.1 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr6:31939880 C>T maps to NM_032454.1 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr7:69364471 G>A maps to NM_015570.2 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr7:69364471 G>A maps to NM_015570.2 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr8:48771463 C>T maps to NM_006904.6 L2096L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr8:48771463 C>T maps to NM_006904.6 L2096L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr8:73849914 G>T maps to NM_004770.2 A775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chr8:73849914 G>T maps to NM_004770.2 A775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chrX:77913338 C>T maps to NM_152694.2 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chrX:77913338 C>T maps to NM_152694.2 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chrX:118797473 G>A maps to ENST00000394612 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chrX:118797473 G>A maps to ENST00000394612 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chrX:120009065 C>T maps to NM_001145718.1 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7864-01A-11D-2229-08 chrX:120009065 C>T maps to NM_001145718.1 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr1:117297335 C>T maps to NM_001767.3 Q49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr1:117297335 C>T maps to NM_001767.3 Q49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr1:231830148 C>T maps to NM_001164537.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr1:231830148 C>T maps to NM_001164537.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr10:81904064 G>A maps to NM_001012973.1 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr10:81904064 G>A maps to NM_001012973.1 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr11:558713 G>A maps to NM_173573.2 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr11:558713 G>A maps to NM_173573.2 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr12:19498822 G>A did not map to a codon.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr12:19498822 G>A did not map to a codon.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr14:20502653 T>C maps to NM_001004714.1 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr14:20502653 T>C maps to NM_001004714.1 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr14:23900627 G>T maps to NM_000257.2 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr14:23900627 G>T maps to NM_000257.2 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr14:91372494 G>A maps to NM_004755.2 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr14:91372494 G>A maps to NM_004755.2 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr14:105415730 C>T maps to NM_138420.2 E2019E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr14:105415730 C>T maps to NM_138420.2 E2019E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr15:25972325 G>A maps to NM_024490.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr15:25972325 G>A maps to NM_024490.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr17:2275525 C>T maps to NM_014853.2 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr17:2275525 C>T maps to NM_014853.2 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr17:2276632 A>G maps to NM_014853.2 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr17:2276632 A>G maps to NM_014853.2 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr17:34964134 C>T maps to NM_024864.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr17:34964134 C>T maps to NM_024864.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr19:18576333 C>T maps to NM_006532.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr19:18576333 C>T maps to NM_006532.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr2:197637641 G>A maps to NM_012086.2 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr2:197637641 G>A maps to NM_012086.2 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr22:46725994 G>T maps to NM_016426.6 E730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr22:46725994 G>T maps to NM_016426.6 E730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr6:108882905 G>A maps to NM_001455.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr6:108882905 G>A maps to NM_001455.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr9:100819143 G>T maps to NM_018946.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr9:100819143 G>T maps to NM_018946.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr1:47606534 C>G maps to NM_001010969.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr1:47606534 C>G maps to NM_001010969.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr1:118583437 T>A maps to NM_206996.2 I1027I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr1:118583437 T>A maps to NM_206996.2 I1027I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr1:153973461 G>A maps to NM_207308.2 Y1752Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr1:153973461 G>A maps to NM_207308.2 Y1752Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr10:105172880 C>T maps to NM_014976.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr10:105172880 C>T maps to NM_014976.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr11:40136522 G>T maps to NM_020929.1 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr11:40136522 G>T maps to NM_020929.1 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr12:52864969 G>C maps to NM_173086.4 Y341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr12:52864969 G>C maps to NM_173086.4 Y341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr12:57866397 G>T maps to ENST00000393797 R790R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr12:57866397 G>T maps to ENST00000393797 R790R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr13:97485338 C>A maps to NM_153456.2 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr13:97485338 C>A maps to NM_153456.2 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr15:26792996 C>A maps to NM_021912.4 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr15:26792996 C>A maps to NM_021912.4 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr15:42631927 T>C maps to NM_198141.2 A635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr15:42631927 T>C maps to NM_198141.2 A635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr18:5394710 C>A maps to NM_012307.2 E1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr18:5394710 C>A maps to NM_012307.2 E1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr18:50451654 G>C maps to NM_005215.3 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr18:50451654 G>C maps to NM_005215.3 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr19:13411422 C>T maps to NM_023035.2 Q744Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr19:13411422 C>T maps to NM_023035.2 Q744Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr19:37904956 G>A maps to NM_152484.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr19:37904956 G>A maps to NM_152484.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr2:11737976 G>T maps to NM_014668.3 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr2:11737976 G>T maps to NM_014668.3 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr2:100203725 G>A maps to NM_001025108.1 D852D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr2:100203725 G>A maps to NM_001025108.1 D852D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr2:141473633 A>T maps to NM_018557.2 I1977I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr2:141473633 A>T maps to NM_018557.2 I1977I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr2:228786233 C>A maps to NM_178821.1 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr2:228786233 C>A maps to NM_178821.1 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr4:72363396 T>C maps to NM_001098484.2 Y718Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr4:72363396 T>C maps to NM_001098484.2 Y718Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr5:140762627 G>T maps to NM_018920.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr5:140762627 G>T maps to NM_018920.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr5:176638367 G>T maps to NM_022455.4 E990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr5:176638367 G>T maps to NM_022455.4 E990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr6:105606551 C>T maps to NM_022361.4 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr6:105606551 C>T maps to NM_022361.4 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr7:57188500 A>G maps to NM_033273.1 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chr7:57188500 A>G maps to NM_033273.1 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chrX:37265459 A>C did not map to a codon.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chrX:37265459 A>C did not map to a codon.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chrX:140985530 C>A maps to NM_138702.1 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7870-01A-11D-2229-08 chrX:140985530 C>A maps to NM_138702.1 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:878708 C>T maps to ENST00000443100 D547D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:878708 C>T maps to ENST00000443100 D547D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:6196850 G>A maps to NM_015557.2 G837G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:6196850 G>A maps to NM_015557.2 G837G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:12907548 C>A maps to NM_001013631.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:12907548 C>A maps to NM_001013631.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:24397717 G>A maps to ENST00000330966 N1014N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:24397717 G>A maps to ENST00000330966 N1014N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:38227326 C>T maps to NM_001099439.1 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:38227326 C>T maps to NM_001099439.1 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:39463963 C>G maps to NM_024595.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:39463963 C>G maps to NM_024595.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:53555530 G>A maps to NM_006671.4 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:53555530 G>A maps to NM_006671.4 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:75038327 G>C maps to NM_001002912.4 A1022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:75038327 G>C maps to NM_001002912.4 A1022A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BB-7871-01A-11D-2229-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BB-7871-01A-11D-2229-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:162337110 G>T maps to NM_014697.2 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:162337110 G>T maps to NM_014697.2 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:240370400 G>C maps to ENST00000406993 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:240370400 G>C maps to ENST00000406993 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr10:28023598 G>T maps to NM_173576.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr10:28023598 G>T maps to NM_173576.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr10:33199264 G>A maps to ENST00000374956 Q684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr10:33199264 G>A maps to ENST00000374956 Q684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr10:34805968 G>C maps to NM_019619.3 S114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr10:34805968 G>C maps to NM_019619.3 S114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr10:87362281 C>G maps to NM_017551.2 S926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr10:87362281 C>G maps to NM_017551.2 S926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr10:131565173 A>T maps to NM_002412.3 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr10:131565173 A>T maps to NM_002412.3 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:2604771 A>T maps to NM_000218.2 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:2604771 A>T maps to NM_000218.2 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:5373441 C>G maps to NM_001004750.1 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:5373441 C>G maps to NM_001004750.1 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:10647887 C>T maps to NM_001098579.1 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:10647887 C>T maps to NM_001098579.1 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:55135909 C>A maps to NM_001005275.1 S184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:55135909 C>A maps to NM_001005275.1 S184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:56954743 C>A maps to NM_001005210.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:56954743 C>A maps to NM_001005210.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:57578935 C>G maps to NM_001085458.1 L872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:57578935 C>G maps to NM_001085458.1 L872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:60182999 G>T maps to NM_032597.3 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:60182999 G>T maps to NM_032597.3 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:76372273 G>A maps to NM_001128922.1 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:76372273 G>A maps to NM_001128922.1 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:130059705 C>T maps to NM_021978.3 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:130059705 C>T maps to NM_021978.3 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:134163102 G>A maps to NM_001080407.2 Q292Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr11:134163102 G>A maps to NM_001080407.2 Q292Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr12:2614033 G>A maps to NM_199460.2 W380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr12:2614033 G>A maps to NM_199460.2 W380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr12:18499617 C>A maps to NM_004570.4 Y491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr12:18499617 C>A maps to NM_004570.4 Y491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr12:105569860 C>T did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr12:105569860 C>T did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr13:109792670 C>A maps to NM_015011.1 R1349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr13:109792670 C>A maps to NM_015011.1 R1349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr14:39721979 G>A maps to NM_054024.3 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr14:39721979 G>A maps to NM_054024.3 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr14:88477766 T>C maps to NM_003608.3 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr14:88477766 T>C maps to NM_003608.3 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr15:45007751 G>T maps to NM_004048.2 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr15:45007751 G>T maps to NM_004048.2 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr15:54305603 C>T maps to ENST00000260323 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr15:54305603 C>T maps to ENST00000260323 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr15:65917056 G>A maps to NM_004727.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr15:65917056 G>A maps to NM_004727.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr15:91021067 G>T maps to NM_003870.3 V1092V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr15:91021067 G>T maps to NM_003870.3 V1092V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr16:2579488 C>A maps to NM_001145815.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr16:2579488 C>A maps to NM_001145815.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr16:80654696 G>T maps to NM_152342.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr16:80654696 G>T maps to NM_152342.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:17030065 G>A maps to NM_015134.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:17030065 G>A maps to NM_015134.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:53108626 T>C did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:53108626 T>C did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:56349014 C>T did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:56349014 C>T did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:57058233 C>T maps to NM_014906.3 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:57058233 C>T maps to NM_014906.3 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:61957806 C>T maps to NM_002059.3 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:61957806 C>T maps to NM_002059.3 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:74625171 C>T maps to NM_018414.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:74625171 C>T maps to NM_018414.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:74625489 C>G maps to NM_018414.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr17:74625489 C>G maps to NM_018414.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr18:19244104 G>A maps to NM_138340.4 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr18:19244104 G>A maps to NM_138340.4 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr18:19427047 C>T maps to NM_020774.2 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr18:19427047 C>T maps to NM_020774.2 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr18:31684008 A>G did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr18:31684008 A>G did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:1062257 G>A maps to NM_019112.3 E1886E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:1062257 G>A maps to NM_019112.3 E1886E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:4280257 C>A maps to NM_020209.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:4280257 C>A maps to NM_020209.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:10071182 C>T maps to NM_015719.3 A1714A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:10071182 C>T maps to NM_015719.3 A1714A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:11031563 G>C maps to NM_199141.1 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:11031563 G>C maps to NM_199141.1 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:22952080 C>A maps to ENST00000397104 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:22952080 C>A maps to ENST00000397104 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:54314432 G>T maps to ENST00000391773 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:54314432 G>T maps to ENST00000391773 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:55451292 C>G maps to ENST00000446217 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr19:55451292 C>G maps to ENST00000446217 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:46007 G>C maps to NM_001077710.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:46007 G>C maps to NM_001077710.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:112933378 A>G maps to NM_153214.2 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:112933378 A>G maps to NM_153214.2 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:176981710 C>A maps to NM_002148.3 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:176981710 C>A maps to NM_002148.3 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:178936873 G>T maps to NM_016953.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:178936873 G>T maps to NM_016953.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:179466433 G>A maps to NM_133378.4 A15893A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:179466433 G>A maps to NM_133378.4 A15893A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:179597006 T>A maps to NM_133378.4 L4319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:179597006 T>A maps to NM_133378.4 L4319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:179598041 G>A maps to NM_133378.4 H4082H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:179598041 G>A maps to NM_133378.4 H4082H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:189962025 C>A maps to NM_000393.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:189962025 C>A maps to NM_000393.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:230636254 G>A maps to ENST00000389044 Q1903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:230636254 G>A maps to ENST00000389044 Q1903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:233986854 G>A maps to ENST00000359570 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:233986854 G>A maps to ENST00000359570 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:238267207 C>A maps to NM_004369.3 G2143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:238267207 C>A maps to NM_004369.3 G2143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr20:45130307 G>C maps to NM_018102.3 S557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr20:45130307 G>C maps to NM_018102.3 S557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr20:45315595 C>G maps to NM_033550.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr20:45315595 C>G maps to NM_033550.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr20:57766301 G>T maps to NM_178457.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr20:57766301 G>T maps to NM_178457.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr20:61288357 G>A maps to NM_016354.3 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr20:61288357 G>A maps to NM_016354.3 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr21:10920131 T>A maps to NM_199261.2 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr21:10920131 T>A maps to NM_199261.2 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr22:50960668 C>T maps to NM_001185011.1 Q408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr22:50960668 C>T maps to NM_001185011.1 Q408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr3:38622703 A>G maps to NM_001099404.1 C982C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr3:38622703 A>G maps to NM_001099404.1 C982C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr3:48687961 C>T maps to NM_001407.2 Q2141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr3:48687961 C>T maps to NM_001407.2 Q2141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr3:48689418 C>T maps to NM_001407.2 V1938V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr3:48689418 C>T maps to NM_001407.2 V1938V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr3:50127885 T>G did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr3:50127885 T>G did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr3:111797613 G>A maps to ENST00000443106 Q738Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr3:111797613 G>A maps to ENST00000443106 Q738Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr3:123023003 G>C maps to NM_183357.2 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr3:123023003 G>C maps to NM_183357.2 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr4:41984474 T>C maps to NM_001029955.3 D222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr4:41984474 T>C maps to NM_001029955.3 D222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr4:75231039 G>A maps to NM_001432.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr4:75231039 G>A maps to NM_001432.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr4:167983652 G>T maps to NM_016950.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr4:167983652 G>T maps to NM_016950.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr5:1282689 C>A maps to NM_198253.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr5:1282689 C>A maps to NM_198253.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr5:90149124 C>A maps to NM_032119.3 C5743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr5:90149124 C>A maps to NM_032119.3 C5743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr5:134343828 G>A maps to NM_178019.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr5:134343828 G>A maps to NM_178019.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr5:137726868 G>A maps to NM_016604.3 Q516Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr5:137726868 G>A maps to NM_016604.3 Q516Q. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BB-7871-01A-11D-2229-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-BB-7871-01A-11D-2229-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:31691749 C>T maps to NM_138272.1 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:31691749 C>T maps to NM_138272.1 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:40399495 G>A maps to NM_020737.1 Q453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:40399495 G>A maps to NM_020737.1 Q453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:42851352 G>T did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:42851352 G>T did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:74073397 C>T maps to NM_001017361.2 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:74073397 C>T maps to NM_001017361.2 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:90411327 G>A maps to NM_014611.1 F2792F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:90411327 G>A maps to NM_014611.1 F2792F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:152647534 G>A maps to NM_182961.2 I5063I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:152647534 G>A maps to NM_182961.2 I5063I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:160645780 C>A maps to NM_003058.3 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr6:160645780 C>A maps to NM_003058.3 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr7:71743728 C>T maps to NM_031468.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr7:71743728 C>T maps to NM_031468.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr7:83014749 C>T did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr7:83014749 C>T did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr7:111395597 G>T maps to ENST00000428084 R1463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr7:111395597 G>T maps to ENST00000428084 R1463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr7:128640491 A>T maps to ENST00000471166 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr7:128640491 A>T maps to ENST00000471166 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr8:61749498 A>G maps to NM_017780.2 L1371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr8:61749498 A>G maps to NM_017780.2 L1371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr8:100443888 A>T maps to NM_017890.3 L1069L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr8:100443888 A>T maps to NM_017890.3 L1069L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr8:143957719 C>T maps to ENST00000377675 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr8:143957719 C>T maps to ENST00000377675 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr8:146068369 G>A maps to ENST00000446747 K636K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr8:146068369 G>A maps to ENST00000446747 K636K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr9:36677295 A>T maps to NM_014791.2 R640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr9:36677295 A>T maps to NM_014791.2 R640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr9:95018989 G>T maps to ENST00000375660 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr9:95018989 G>T maps to ENST00000375660 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr9:101540675 G>A maps to ENST00000375018 R467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr9:101540675 G>A maps to ENST00000375018 R467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr9:131365868 G>A maps to NM_001130438.2 K1209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr9:131365868 G>A maps to NM_001130438.2 K1209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr9:136641199 C>A maps to NM_001134398.1 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr9:136641199 C>A maps to NM_001134398.1 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chrX:22132679 C>G maps to NM_000444.4 Y426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chrX:22132679 C>G maps to NM_000444.4 Y426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chrX:65417621 T>A maps to NM_138737.3 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chrX:65417621 T>A maps to NM_138737.3 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chrX:91132396 G>C maps to NM_032968.3 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chrX:91132396 G>C maps to NM_032968.3 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chrX:138714491 A>T did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chrX:138714491 A>T did not map to a codon.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr1:100349944 C>T maps to ENST00000311030 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr1:100349944 C>T maps to ENST00000311030 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr1:150337288 G>T maps to NM_015203.3 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr1:150337288 G>T maps to NM_015203.3 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr1:205566947 C>T maps to NM_181644.4 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr1:205566947 C>T maps to NM_181644.4 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr1:242277313 G>C maps to NM_152666.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr1:242277313 G>C maps to NM_152666.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr11:67787206 C>T maps to NM_001161473.1 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr11:67787206 C>T maps to NM_001161473.1 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr11:123513319 C>T maps to NM_018400.3 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr11:123513319 C>T maps to NM_018400.3 Q93Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr13:100635304 C>T maps to NM_007129.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr13:100635304 C>T maps to NM_007129.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr15:41767763 C>G maps to NM_015138.4 S443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr15:41767763 C>G maps to NM_015138.4 S443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr15:75185034 C>T maps to NM_002435.1 Q127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr15:75185034 C>T maps to NM_002435.1 Q127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr17:31322640 C>T maps to NM_173847.3 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr17:31322640 C>T maps to NM_173847.3 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr2:119914518 G>A maps to NM_182528.3 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr2:119914518 G>A maps to NM_182528.3 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr2:242154317 G>A did not map to a codon.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr2:242154317 G>A did not map to a codon.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr4:187539650 C>A maps to ENST00000260147 E2700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr4:187539650 C>A maps to ENST00000260147 E2700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr5:140580942 C>T maps to NM_018931.2 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr5:140580942 C>T maps to NM_018931.2 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr7:15652167 C>T maps to NM_005924.4 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr7:15652167 C>T maps to NM_005924.4 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr7:93055793 C>T maps to NM_001164737.1 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr7:93055793 C>T maps to NM_001164737.1 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr8:37756683 C>T maps to NM_001002814.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr8:37756683 C>T maps to NM_001002814.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr8:101153495 G>C maps to NM_001029860.3 S329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr8:101153495 G>C maps to NM_001029860.3 S329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr9:139407989 C>T did not map to a codon.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chr9:139407989 C>T did not map to a codon.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chrX:79281197 G>A maps to NM_016954.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chrX:79281197 G>A maps to NM_016954.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chrX:117043644 G>A maps to NM_033495.3 Q329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chrX:117043644 G>A maps to NM_033495.3 Q329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chrX:118920676 T>C maps to ENST00000422326 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chrX:118920676 T>C maps to ENST00000422326 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chrX:139585911 G>A maps to NM_005634.2 N438N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7872-01A-11D-2229-08 chrX:139585911 G>A maps to NM_005634.2 N438N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:909867 C>T maps to ENST00000379409 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:909867 C>T maps to ENST00000379409 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:6648383 C>T maps to NM_005341.2 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:6648383 C>T maps to NM_005341.2 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:12726744 G>A maps to NM_001013630.1 *408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:12726744 G>A maps to NM_001013630.1 *408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:12835019 C>T maps to NM_001080830.1 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:12835019 C>T maps to NM_001080830.1 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:21031009 G>A maps to NM_020816.2 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:21031009 G>A maps to NM_020816.2 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:22329568 C>T maps to NM_005747.4 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:22329568 C>T maps to NM_005747.4 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:28806961 G>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:28806961 G>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:34667793 C>G maps to NM_001134734.1 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:34667793 C>G maps to NM_001134734.1 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:38449852 C>T maps to NM_006802.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:38449852 C>T maps to NM_006802.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:39792904 G>A maps to ENST00000361689 E1503E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:39792904 G>A maps to ENST00000361689 E1503E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:40703618 C>G maps to NM_012421.3 S1082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:40703618 C>G maps to NM_012421.3 S1082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:43636429 C>T maps to NM_001159936.1 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:43636429 C>T maps to NM_001159936.1 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:53373582 C>G maps to ENST00000371522 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:53373582 C>G maps to ENST00000371522 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:54269610 G>C maps to NM_018087.4 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:54269610 G>C maps to NM_018087.4 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:55089032 G>C maps to NM_176782.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:55089032 G>C maps to NM_176782.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:67340501 G>A maps to NM_024763.4 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:67340501 G>A maps to NM_024763.4 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:68897199 C>T maps to NM_000329.2 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:68897199 C>T maps to NM_000329.2 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:90401041 G>A maps to NM_001134479.1 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:90401041 G>A maps to NM_001134479.1 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:144882643 C>G maps to NM_014644.4 L1125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:144882643 C>G maps to NM_014644.4 L1125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:146763162 G>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:146763162 G>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:149859410 G>T maps to NM_175065.2 S19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:149859410 G>T maps to NM_175065.2 S19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:150131447 G>A maps to ENST00000443480 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:150131447 G>A maps to ENST00000443480 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:151491281 C>G maps to NM_020770.2 S96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:151491281 C>G maps to NM_020770.2 S96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:152281431 G>C maps to NM_002016.1 S1977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:152281431 G>C maps to NM_002016.1 S1977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:154197668 C>T maps to NM_014847.3 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:154197668 C>T maps to NM_014847.3 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:154223668 C>T maps to NM_014847.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:154223668 C>T maps to NM_014847.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:155034447 G>A maps to NM_207197.1 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:155034447 G>A maps to NM_207197.1 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:158262650 C>T maps to NM_001765.2 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:158262650 C>T maps to NM_001765.2 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:158812161 A>G maps to NM_002432.1 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:158812161 A>G maps to NM_002432.1 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:172539801 G>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:172539801 G>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:180243596 G>C maps to NM_033343.3 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:180243596 G>C maps to NM_033343.3 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:182869252 G>C maps to ENST00000287709 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:182869252 G>C maps to ENST00000287709 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:185143908 A>G maps to NM_001105518.1 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:185143908 A>G maps to NM_001105518.1 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:202861735 G>A maps to NM_021633.2 I544I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:202861735 G>A maps to NM_021633.2 I544I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:208218432 G>A maps to NM_025179.3 L1206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:208218432 G>A maps to NM_025179.3 L1206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:232601013 G>T maps to NM_020808.3 R798R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:232601013 G>T maps to NM_020808.3 R798R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:243504339 G>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr1:243504339 G>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:12162208 G>A maps to NM_018706.5 Q867Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:12162208 G>A maps to NM_018706.5 Q867Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:15115167 G>A maps to NM_018324.2 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:15115167 G>A maps to NM_018324.2 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:17747603 C>G maps to NM_003473.2 S358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:17747603 C>G maps to NM_003473.2 S358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:34649065 G>C maps to NM_019619.3 S610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:34649065 G>C maps to NM_019619.3 S610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:45498927 C>T maps to NM_006963.4 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:45498927 C>T maps to NM_006963.4 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:95372754 C>G maps to NM_006204.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:95372754 C>G maps to NM_006204.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:105209671 G>A maps to NM_015916.4 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:105209671 G>A maps to NM_015916.4 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:121436716 C>T maps to NM_004281.3 Q551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:121436716 C>T maps to NM_004281.3 Q551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:124800175 C>G maps to NM_001609.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:124800175 C>G maps to NM_001609.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:126681774 G>A maps to NM_022802.2 I885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:126681774 G>A maps to NM_022802.2 I885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:133930804 C>G maps to NM_001105521.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:133930804 C>G maps to NM_001105521.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:135106654 C>T maps to NM_006659.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:135106654 C>T maps to NM_006659.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:135212702 G>C maps to NM_138384.2 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr10:135212702 G>C maps to NM_138384.2 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:407114 G>A maps to NM_021805.2 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:407114 G>A maps to NM_021805.2 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:691545 G>A maps to NM_021008.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:691545 G>A maps to NM_021008.2 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:1774753 G>A maps to NM_001909.3 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:1774753 G>A maps to NM_001909.3 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:5142421 C>T maps to NM_001005222.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:5142421 C>T maps to NM_001005222.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:5701230 C>G maps to NM_033034.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:5701230 C>G maps to NM_033034.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:6587844 G>C maps to NM_144666.2 L3745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:6587844 G>C maps to NM_144666.2 L3745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:6866954 C>T maps to ENST00000379831 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:6866954 C>T maps to ENST00000379831 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:31312292 C>T maps to NM_181807.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:31312292 C>T maps to NM_181807.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:32676498 G>C maps to NM_001008391.2 S222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:32676498 G>C maps to NM_001008391.2 S222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:46801863 C>G maps to ENST00000415402 V771V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:46801863 C>G maps to ENST00000415402 V771V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:47176812 G>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:47176812 G>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:55135370 G>A maps to NM_001005275.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:55135370 G>A maps to NM_001005275.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:55579556 G>A maps to NM_001004738.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:55579556 G>A maps to NM_001004738.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:55659077 C>T maps to NM_032681.3 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:55659077 C>T maps to NM_032681.3 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:57982932 G>A maps to NM_001004458.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:57982932 G>A maps to NM_001004458.1 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:62364200 C>A maps to NM_004739.2 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:62364200 C>A maps to NM_004739.2 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:62444319 G>C maps to NM_015853.3 S270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:62444319 G>C maps to NM_015853.3 S270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:66985206 C>T maps to NM_012308.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:66985206 C>T maps to NM_012308.2 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:68575045 C>G maps to NM_001876.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:68575045 C>G maps to NM_001876.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:76062411 G>A maps to NM_004705.2 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:76062411 G>A maps to NM_004705.2 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:77378292 G>C maps to NM_016578.3 S1332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:77378292 G>C maps to NM_016578.3 S1332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:93523942 G>A maps to NM_004268.4 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:93523942 G>A maps to NM_004268.4 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:99786822 C>T maps to NM_014361.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:99786822 C>T maps to NM_014361.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:113816675 C>T maps to NM_006028.3 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:113816675 C>T maps to NM_006028.3 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:116730263 G>A maps to ENST00000445177 Q821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:116730263 G>A maps to ENST00000445177 Q821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:117098988 C>T maps to NM_004716.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:117098988 C>T maps to NM_004716.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:118499168 C>T maps to NM_015157.2 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:118499168 C>T maps to NM_015157.2 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:119185720 G>A maps to NM_006500.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:119185720 G>A maps to NM_006500.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:125830979 C>A maps to ENST00000392693 E1241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:125830979 C>A maps to ENST00000392693 E1241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:134182364 C>T maps to NM_001080407.2 H470H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr11:134182364 C>T maps to NM_001080407.2 H470H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:1943842 G>T maps to NM_001163926.1 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:1943842 G>T maps to NM_001163926.1 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:6952354 C>A maps to NM_002075.2 S74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:6952354 C>A maps to NM_002075.2 S74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:8906663 G>C maps to NM_020734.2 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:8906663 G>C maps to NM_020734.2 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:9227269 G>C maps to NM_000014.4 L1214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:9227269 G>C maps to NM_000014.4 L1214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:9751249 C>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:9751249 C>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:10251524 G>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:10251524 G>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:10783758 T>C maps to NM_018423.2 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:10783758 T>C maps to NM_018423.2 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:10959147 G>C maps to NM_023918.1 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:10959147 G>C maps to NM_023918.1 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:39713803 G>C maps to ENST00000395670 S1228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:39713803 G>C maps to ENST00000395670 S1228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:49942876 C>T maps to NM_012284.1 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:49942876 C>T maps to NM_012284.1 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:64818848 G>T maps to NM_007235.3 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:64818848 G>T maps to NM_007235.3 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:77216298 G>A maps to NM_015336.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:77216298 G>A maps to NM_015336.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:108134780 G>A maps to NM_012406.3 F622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:108134780 G>A maps to NM_012406.3 F622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:112711539 G>A maps to NM_001109662.2 Q439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:112711539 G>A maps to NM_001109662.2 Q439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:114837438 T>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:114837438 T>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:21729930 G>C maps to NM_145061.5 S380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:21729930 G>C maps to NM_145061.5 S380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:25448362 C>A maps to ENST00000381927 S1569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:25448362 C>A maps to ENST00000381927 S1569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:32776557 C>G maps to NM_023037.2 L1304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:32776557 C>G maps to NM_023037.2 L1304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:38153455 C>T maps to NM_006475.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:38153455 C>T maps to NM_006475.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:42393494 G>A maps to NM_015058.1 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:42393494 G>A maps to NM_015058.1 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:45008998 C>T maps to NM_183422.2 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:45008998 C>T maps to NM_183422.2 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:52348131 C>T maps to NM_001031719.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:52348131 C>T maps to NM_001031719.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:96743703 C>G maps to NM_153456.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:96743703 C>G maps to NM_153456.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:111927982 C>T maps to NM_001113511.1 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr13:111927982 C>T maps to NM_001113511.1 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:23882970 C>G maps to NM_000257.2 T1929T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:23882970 C>G maps to NM_000257.2 T1929T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:47120417 C>T maps to NM_080746.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:47120417 C>T maps to NM_080746.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:52182161 C>G maps to ENST00000344768 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:52182161 C>G maps to ENST00000344768 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:53513590 C>T maps to NM_001160148.1 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:53513590 C>T maps to NM_001160148.1 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:57052605 C>G maps to NM_017799.3 S107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:57052605 C>G maps to NM_017799.3 S107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:60619716 G>A maps to NM_016029.2 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:60619716 G>A maps to NM_016029.2 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:68043189 G>T maps to NM_020715.2 G811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:68043189 G>T maps to NM_020715.2 G811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:74125576 G>T maps to NM_031427.2 E24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:74125576 G>T maps to NM_031427.2 E24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:77269771 G>A maps to NM_015305.3 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:77269771 G>A maps to NM_015305.3 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:78374174 G>A maps to NM_020421.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:78374174 G>A maps to NM_020421.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:95235375 G>A maps to NM_173849.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:95235375 G>A maps to NM_173849.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:96848582 G>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:96848582 G>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:104129087 C>T maps to ENST00000445352 Y379Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:104129087 C>T maps to ENST00000445352 Y379Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:22993079 G>A maps to NM_014608.2 L989L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:22993079 G>A maps to NM_014608.2 L989L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:44058970 C>G maps to NM_005313.4 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:44058970 C>G maps to NM_005313.4 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:65499132 G>A maps to NM_003613.3 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:65499132 G>A maps to NM_003613.3 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:72582345 C>T maps to NM_052840.4 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:72582345 C>T maps to NM_052840.4 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:75189513 C>G maps to NM_002435.1 S336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:75189513 C>G maps to NM_002435.1 S336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:75668137 C>T maps to NM_001145357.1 K1153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:75668137 C>T maps to NM_001145357.1 K1153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:85360148 G>T maps to NM_020778.4 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:85360148 G>T maps to NM_020778.4 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:91488218 C>T maps to NM_018671.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:91488218 C>T maps to NM_018671.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:102264440 G>C maps to NM_152334.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr15:102264440 G>C maps to NM_152334.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:4797505 C>G maps to NM_139170.2 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:4797505 C>G maps to NM_139170.2 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:14755858 C>T maps to NM_016561.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:14755858 C>T maps to NM_016561.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:19087179 C>T maps to NM_016138.4 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:19087179 C>T maps to NM_016138.4 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:20570613 C>G maps to NM_182617.3 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:20570613 C>G maps to NM_182617.3 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:30712175 C>T maps to NM_006662.2 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:30712175 C>T maps to NM_006662.2 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:46763018 G>A maps to NM_182493.2 I563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:46763018 G>A maps to NM_182493.2 I563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:47488013 G>A maps to NM_030790.3 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:47488013 G>A maps to NM_030790.3 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:48596100 C>T maps to NM_153029.3 Q151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:48596100 C>T maps to NM_153029.3 Q151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:55899898 C>T maps to NM_001143685.1 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:55899898 C>T maps to NM_001143685.1 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:56996943 G>C maps to NM_000078.2 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:56996943 G>C maps to NM_000078.2 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:69148600 G>A maps to NM_005329.2 W365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:69148600 G>A maps to NM_005329.2 W365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:71054109 C>T maps to NM_032821.2 E1099E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:71054109 C>T maps to NM_032821.2 E1099E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:71418696 G>A maps to NM_001740.4 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr16:71418696 G>A maps to NM_001740.4 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:1635681 C>T maps to NM_001163809.1 L1407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:1635681 C>T maps to NM_001163809.1 L1407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:5086385 G>C maps to NM_032530.1 S389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:5086385 G>C maps to NM_032530.1 S389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:7128358 C>T maps to ENST00000356839 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:7128358 C>T maps to ENST00000356839 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:10415429 G>A maps to NM_005963.3 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:10415429 G>A maps to NM_005963.3 V409V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CN-4723-01A-01D-1434-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CN-4723-01A-01D-1434-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:11631205 C>T maps to NM_001372.3 I1927I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:11631205 C>T maps to NM_001372.3 I1927I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:11835354 G>T maps to NM_001372.3 E4044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:11835354 G>T maps to NM_001372.3 E4044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:19470500 C>T maps to ENST00000395585 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:19470500 C>T maps to ENST00000395585 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:34499236 G>A maps to NM_001001417.5 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:34499236 G>A maps to NM_001001417.5 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:36104542 G>A maps to NM_000458.2 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:36104542 G>A maps to NM_000458.2 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:39503387 C>G maps to NM_004138.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:39503387 C>G maps to NM_004138.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:45787868 G>C maps to NM_014726.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:45787868 G>C maps to NM_014726.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:48050614 C>T maps to NM_138281.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:48050614 C>T maps to NM_138281.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:48649386 G>A maps to NM_018896.3 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:48649386 G>A maps to NM_018896.3 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:56540555 G>A maps to NM_001080439.1 Q377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:56540555 G>A maps to NM_001080439.1 Q377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:60088193 G>A maps to NM_005121.2 Q562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:60088193 G>A maps to NM_005121.2 Q562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:65156471 G>A maps to NM_014877.3 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:65156471 G>A maps to NM_014877.3 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:76121047 C>T maps to NM_007267.6 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr17:76121047 C>T maps to NM_007267.6 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr18:5410588 G>A maps to NM_012307.2 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr18:5410588 G>A maps to NM_012307.2 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr18:9570205 C>A maps to NM_001042388.1 E508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr18:9570205 C>A maps to NM_001042388.1 E508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr18:46905006 G>A maps to NM_017653.3 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr18:46905006 G>A maps to NM_017653.3 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr18:72343889 A>G maps to NM_017757.2 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr18:72343889 A>G maps to NM_017757.2 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:900135 G>C maps to NM_138774.3 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:900135 G>C maps to NM_138774.3 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:1254428 C>T maps to NM_177401.4 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:1254428 C>T maps to NM_177401.4 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:5456014 G>A maps to NM_181710.3 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:5456014 G>A maps to NM_181710.3 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:6427440 G>A maps to NM_173637.3 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:6427440 G>A maps to NM_173637.3 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:9062945 G>C maps to NM_024690.2 S8167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:9062945 G>C maps to NM_024690.2 S8167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:9578056 C>T maps to NM_152476.2 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:9578056 C>T maps to NM_152476.2 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:10675659 C>T maps to NM_023008.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:10675659 C>T maps to NM_023008.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:10689576 G>A maps to ENST00000453102 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:10689576 G>A maps to ENST00000453102 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:12721449 G>C maps to NM_020714.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:12721449 G>C maps to NM_020714.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:15547893 G>A maps to ENST00000389282 F773F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:15547893 G>A maps to ENST00000389282 F773F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:37383091 G>A maps to NM_001171979.1 R282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:37383091 G>A maps to NM_001171979.1 R282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:40430301 A>G maps to NM_003890.2 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:40430301 A>G maps to NM_003890.2 V547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:42600359 G>C maps to ENST00000342301 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:42600359 G>C maps to ENST00000342301 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:43268173 C>T maps to NM_182707.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:43268173 C>T maps to NM_182707.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:45579001 G>C maps to NM_145288.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:45579001 G>C maps to NM_145288.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:50549103 C>T maps to NM_015428.1 F468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:50549103 C>T maps to NM_015428.1 F468F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:51022333 G>A maps to NM_001080457.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:51022333 G>A maps to NM_001080457.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:52724382 C>A maps to NM_014225.5 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:52724382 C>A maps to NM_014225.5 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:52941052 C>T maps to NM_001143939.1 Q127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:52941052 C>T maps to NM_001143939.1 Q127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:53117231 G>A maps to NM_018300.3 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:53117231 G>A maps to NM_018300.3 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:55340900 C>G maps to NM_013289.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:55340900 C>G maps to NM_013289.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:55756737 G>A maps to ENST00000443936 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:55756737 G>A maps to ENST00000443936 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:55853366 C>T maps to NM_032701.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:55853366 C>T maps to NM_032701.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:56423802 G>A maps to NM_176810.2 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:56423802 G>A maps to NM_176810.2 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:57883218 C>T maps to NM_173631.2 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:57883218 C>T maps to NM_173631.2 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:20818830 C>T maps to NM_022460.3 Q365Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:20818830 C>T maps to NM_022460.3 Q365Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:24985572 G>A maps to NM_003743.4 L1361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:24985572 G>A maps to NM_003743.4 L1361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:33752313 G>A maps to NM_170672.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:33752313 G>A maps to NM_170672.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:44161340 C>T maps to NM_133259.3 K908K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:44161340 C>T maps to NM_133259.3 K908K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:44549939 C>G maps to NM_001171603.1 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:44549939 C>G maps to NM_001171603.1 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:48698495 C>T maps to NM_001135629.2 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:48698495 C>T maps to NM_001135629.2 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:48809195 C>G maps to NM_172311.2 S475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:48809195 C>G maps to NM_172311.2 S475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:73470150 C>G maps to NM_006429.3 S96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:73470150 C>G maps to NM_006429.3 S96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:73651681 C>T maps to NM_015120.4 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:73651681 C>T maps to NM_015120.4 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:96690535 G>T maps to NM_207328.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:96690535 G>T maps to NM_207328.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:103068541 C>T maps to NM_003853.2 F567F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:103068541 C>T maps to NM_003853.2 F567F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:128366311 G>A maps to ENST00000389524 Q891Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:128366311 G>A maps to ENST00000389524 Q891Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:133541611 C>T maps to NM_207363.2 V924V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:133541611 C>T maps to NM_207363.2 V924V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:135745718 G>C maps to NM_025052.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:135745718 G>C maps to NM_025052.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:153415271 G>C maps to NM_052905.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:153415271 G>C maps to NM_052905.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:158399268 G>C maps to NM_145259.2 S350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:158399268 G>C maps to NM_145259.2 S350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:164466132 G>A maps to NM_018086.2 Q737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:164466132 G>A maps to NM_018086.2 Q737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:175006585 C>G maps to ENST00000409546 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:175006585 C>G maps to ENST00000409546 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:178977395 G>C maps to ENST00000456670 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:178977395 G>C maps to ENST00000456670 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:179616569 T>C maps to ENST00000375038 E3521E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:179616569 T>C maps to ENST00000375038 E3521E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:179650576 G>A maps to NM_133378.4 Q790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:179650576 G>A maps to NM_133378.4 Q790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:190927052 C>G maps to NM_005259.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:190927052 C>G maps to NM_005259.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:191929549 G>A maps to NM_003151.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:191929549 G>A maps to NM_003151.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:196661352 G>A maps to NM_018897.2 Q3488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:196661352 G>A maps to NM_018897.2 Q3488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:212530142 T>C maps to NM_005235.2 K592K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:212530142 T>C maps to NM_005235.2 K592K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:219529907 C>G maps to NM_022453.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:219529907 C>G maps to NM_022453.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:228128541 G>C maps to NM_000091.4 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:228128541 G>C maps to NM_000091.4 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:234591191 C>T maps to ENST00000373460 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:234591191 C>T maps to ENST00000373460 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:234669409 C>T maps to NM_000463.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:234669409 C>T maps to NM_000463.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:239342303 C>T maps to NM_001040445.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:239342303 C>T maps to NM_001040445.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:241534073 C>G maps to NM_023083.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:241534073 C>G maps to NM_023083.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr20:2464517 G>A maps to NM_024325.4 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr20:2464517 G>A maps to NM_024325.4 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr20:2640907 C>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr20:2640907 C>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr20:3581668 C>G maps to NM_139321.2 S1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr20:3581668 C>G maps to NM_139321.2 S1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr20:10653357 G>A maps to NM_000214.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr20:10653357 G>A maps to NM_000214.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr20:44512004 C>G maps to NM_080603.4 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr20:44512004 C>G maps to NM_080603.4 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr20:61594628 C>T maps to NM_022082.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr20:61594628 C>T maps to NM_022082.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr20:62234365 G>T maps to NM_012384.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr20:62234365 G>T maps to NM_012384.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr21:28338536 G>A maps to NM_007038.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr21:28338536 G>A maps to NM_007038.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr21:33671365 G>A maps to ENST00000445271 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr21:33671365 G>A maps to ENST00000445271 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr21:40574318 G>C maps to NM_018963.3 S1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr21:40574318 G>C maps to NM_018963.3 S1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr21:42823124 G>A maps to NM_001144925.1 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr21:42823124 G>A maps to NM_001144925.1 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr21:44841566 G>C maps to NM_173354.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr21:44841566 G>C maps to NM_173354.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr21:45107739 G>A maps to NM_015056.2 E495E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr21:45107739 G>A maps to NM_015056.2 E495E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr21:45838390 C>T maps to ENST00000397932 F1138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr21:45838390 C>T maps to ENST00000397932 F1138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr22:17601078 G>A maps to NM_031890.3 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr22:17601078 G>A maps to NM_031890.3 F313F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr22:31091252 C>T maps to NM_030758.3 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr22:31091252 C>T maps to NM_030758.3 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr22:35817334 C>T maps to NM_006739.3 I619I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr22:35817334 C>T maps to NM_006739.3 I619I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr22:36708219 G>A maps to NM_002473.4 F534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr22:36708219 G>A maps to NM_002473.4 F534F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr22:37888525 G>A maps to NM_014550.3 S889S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr22:37888525 G>A maps to NM_014550.3 S889S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr22:43287097 G>T maps to NM_001184970.1 S103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr22:43287097 G>T maps to NM_001184970.1 S103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr22:50718103 G>C maps to NM_012401.2 L1448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr22:50718103 G>C maps to NM_012401.2 L1448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:10291084 G>A maps to NM_014760.3 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:10291084 G>A maps to NM_014760.3 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:17056234 C>T maps to NM_001144382.1 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:17056234 C>T maps to NM_001144382.1 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:39184824 G>C maps to NM_033027.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:39184824 G>C maps to NM_033027.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:47045663 C>T maps to NM_015175.1 I1993I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:47045663 C>T maps to NM_015175.1 I1993I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:50145725 C>G maps to NM_005778.2 S394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:50145725 C>G maps to NM_005778.2 S394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:52240615 C>T maps to ENST00000441729 N355N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:52240615 C>T maps to ENST00000441729 N355N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:63982083 G>A maps to NM_001177387.1 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:63982083 G>A maps to NM_001177387.1 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:107520041 G>C maps to NM_001142568.1 R884R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:107520041 G>C maps to NM_001142568.1 R884R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:124951512 G>C maps to NM_021964.2 S686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:124951512 G>C maps to NM_021964.2 S686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:130281984 G>A maps to NM_001102608.1 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:130281984 G>A maps to NM_001102608.1 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:130686023 G>C maps to NM_001001486.1 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:130686023 G>C maps to NM_001001486.1 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:151155739 C>T maps to NM_178822.4 V2203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:151155739 C>T maps to NM_178822.4 V2203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:183756392 C>T maps to NM_001145143.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:183756392 C>T maps to NM_001145143.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:183777426 C>T maps to NM_130770.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:183777426 C>T maps to NM_130770.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:184026288 G>A maps to NM_002808.3 Q826Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:184026288 G>A maps to NM_002808.3 Q826Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:184033994 C>T maps to NM_001194947.1 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:184033994 C>T maps to NM_001194947.1 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:194140609 G>A maps to NM_024524.3 Q1134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:194140609 G>A maps to NM_024524.3 Q1134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:196656541 C>G maps to NM_152699.4 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr3:196656541 C>G maps to NM_152699.4 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:651153 C>T maps to NM_000283.3 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:651153 C>T maps to NM_000283.3 F424F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:6114559 C>G maps to NM_001099433.1 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:6114559 C>G maps to NM_001099433.1 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:9784234 A>G maps to NM_000798.4 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:9784234 A>G maps to NM_000798.4 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:55136803 C>T maps to NM_006206.4 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:55136803 C>T maps to NM_006206.4 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:56225582 C>T maps to NM_024592.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:56225582 C>T maps to NM_024592.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:70361537 C>T maps to NM_021139.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:70361537 C>T maps to NM_021139.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:79321967 C>T maps to NM_025074.6 I1352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:79321967 C>T maps to NM_025074.6 I1352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:81188025 C>T maps to NM_004464.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:81188025 C>T maps to NM_004464.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:104054925 G>A maps to NM_001813.2 Q2216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:104054925 G>A maps to NM_001813.2 Q2216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:119256646 G>C maps to NM_003619.3 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:119256646 G>C maps to NM_003619.3 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:126329824 C>T maps to NM_024582.4 F1932F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:126329824 C>T maps to NM_024582.4 F1932F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:148944412 G>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:148944412 G>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:151186874 C>A maps to NM_006726.3 *2864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:151186874 C>A maps to NM_006726.3 *2864L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:151509250 G>C maps to NM_006726.3 L2104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:151509250 G>C maps to NM_006726.3 L2104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:174449900 C>T maps to NM_021973.2 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:174449900 C>T maps to NM_021973.2 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:174449905 C>A maps to NM_021973.2 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr4:174449905 C>A maps to NM_021973.2 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:1239638 C>T maps to NM_182632.2 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:1239638 C>T maps to NM_182632.2 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:5461060 G>A maps to NM_015325.1 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:5461060 G>A maps to NM_015325.1 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:9044560 G>T maps to NM_003966.2 S1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:9044560 G>T maps to NM_003966.2 S1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:35010166 C>A maps to NM_031900.3 E426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:35010166 C>A maps to NM_031900.3 E426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:35910093 G>A maps to NM_144647.3 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:35910093 G>A maps to NM_144647.3 I133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:37302929 G>C maps to NM_153485.1 S1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:37302929 G>C maps to NM_153485.1 S1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:43659376 C>T maps to NM_182977.2 L853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:43659376 C>T maps to NM_182977.2 L853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:45396680 G>C maps to NM_021072.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:45396680 G>C maps to NM_021072.2 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:54569132 T>A maps to NM_019030.2 P921P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:54569132 T>A maps to NM_019030.2 P921P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:64910039 G>C maps to NM_001656.3 S84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:64910039 G>C maps to NM_001656.3 S84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:76700609 C>T maps to NM_003719.3 R426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:76700609 C>T maps to NM_003719.3 R426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:79034790 C>T maps to NM_153610.3 I3401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:79034790 C>T maps to NM_153610.3 I3401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:115361748 G>A maps to NM_173800.4 K969K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:115361748 G>A maps to NM_173800.4 K969K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:118176650 G>C maps to NM_173666.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:118176650 G>C maps to NM_173666.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:120021839 G>A maps to NM_016644.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:120021839 G>A maps to NM_016644.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:123983565 C>A maps to NM_020747.2 G837G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:123983565 C>A maps to NM_020747.2 G837G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:140348752 C>G maps to NM_018899.5 S801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:140348752 C>G maps to NM_018899.5 S801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:140481672 A>G maps to NM_018937.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:140481672 A>G maps to NM_018937.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:140604129 G>A maps to NM_018934.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:140604129 G>A maps to NM_018934.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:140720877 C>T maps to NM_018915.2 I780I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:140720877 C>T maps to NM_018915.2 I780I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:150415256 G>A maps to NM_006058.3 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:150415256 G>A maps to NM_006058.3 F469F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:150664218 C>T maps to NM_001145017.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:150664218 C>T maps to NM_001145017.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:153755895 C>T maps to NM_198321.3 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr5:153755895 C>T maps to NM_198321.3 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:28097415 C>T maps to NM_025231.1 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:28097415 C>T maps to NM_025231.1 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:31797592 C>T maps to NM_005346.4 F622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:31797592 C>T maps to NM_005346.4 F622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:33135223 C>G maps to NM_080680.2 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:33135223 C>G maps to NM_080680.2 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:33662852 C>G maps to ENST00000374316 L2646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:33662852 C>G maps to ENST00000374316 L2646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:33995957 C>T maps to NM_000841.1 K876K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:33995957 C>T maps to NM_000841.1 K876K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:41767598 G>A maps to ENST00000373009 Q547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:41767598 G>A maps to ENST00000373009 Q547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:43015984 C>T maps to NM_001168370.1 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:43015984 C>T maps to NM_001168370.1 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:46657052 G>A maps to NM_001010870.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:46657052 G>A maps to NM_001010870.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:52133881 A>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:52133881 A>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:97246863 G>C maps to NM_030784.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:97246863 G>C maps to NM_030784.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:99282854 G>T maps to NM_005604.2 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:99282854 G>T maps to NM_005604.2 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:117232166 C>T maps to NM_173560.3 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:117232166 C>T maps to NM_173560.3 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:130425590 C>G maps to NM_032438.2 S586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:130425590 C>G maps to NM_032438.2 S586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:146673563 C>T maps to NM_000838.3 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:146673563 C>T maps to NM_000838.3 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:159654084 C>T maps to NM_032532.2 S847S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:159654084 C>T maps to NM_032532.2 S847S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:160977187 C>T maps to NM_005577.2 R1614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:160977187 C>T maps to NM_005577.2 R1614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:161157958 G>A maps to NM_000301.3 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:161157958 G>A maps to NM_000301.3 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:161470019 C>G maps to NM_005922.2 S239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:161470019 C>G maps to NM_005922.2 S239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:166918076 G>A maps to ENST00000510118 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:166918076 G>A maps to ENST00000510118 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:167787922 G>C maps to NM_004610.3 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr6:167787922 G>C maps to NM_004610.3 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:794331 G>A maps to NM_017802.3 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:794331 G>A maps to NM_017802.3 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:912961 C>G maps to ENST00000456758 V973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:912961 C>G maps to ENST00000456758 V973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:1486398 C>G maps to NM_182924.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:1486398 C>G maps to NM_182924.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:5340093 G>C maps to NM_153247.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:5340093 G>C maps to NM_153247.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:5662574 G>A maps to NM_207111.2 V896V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:5662574 G>A maps to NM_207111.2 V896V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:18624935 G>T maps to NM_178425.2 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:18624935 G>T maps to NM_178425.2 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:24703279 G>A maps to ENST00000409253 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:24703279 G>A maps to ENST00000409253 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:35242186 G>T maps to NM_001077653.2 S400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:35242186 G>T maps to NM_001077653.2 S400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:40134275 C>T maps to NM_003718.4 L1412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:40134275 C>T maps to NM_003718.4 L1412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:73523308 C>G maps to NM_002314.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:73523308 C>G maps to NM_002314.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:82474790 C>T maps to NM_033026.5 A4614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:82474790 C>T maps to NM_033026.5 A4614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:86468290 A>T maps to NM_000840.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:86468290 A>T maps to NM_000840.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:100683465 T>C maps to NM_001040105.1 P2923P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:100683465 T>C maps to NM_001040105.1 P2923P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:100684032 C>G maps to NM_001040105.1 V3112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:100684032 C>G maps to NM_001040105.1 V3112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:105624677 C>T maps to NM_152750.4 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:105624677 C>T maps to NM_152750.4 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:117243762 G>A maps to NM_000492.3 S945S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:117243762 G>A maps to NM_000492.3 S945S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:137028319 G>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:137028319 G>C did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:138235860 G>A maps to NM_015905.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:138235860 G>A maps to NM_015905.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:141752581 A>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:141752581 A>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:150916224 C>T maps to NM_005692.3 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr7:150916224 C>T maps to NM_005692.3 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:8560294 C>A maps to NM_194284.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:8560294 C>A maps to NM_194284.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:16850802 G>T maps to NM_019851.2 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:16850802 G>T maps to NM_019851.2 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:21891773 G>A maps to NM_182795.1 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:21891773 G>A maps to NM_182795.1 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:56015533 C>T maps to NM_052898.1 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:56015533 C>T maps to NM_052898.1 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:67547414 G>C maps to NM_025054.4 S997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:67547414 G>C maps to NM_025054.4 S997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:72942204 C>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:72942204 C>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:72981314 G>A maps to NM_007332.2 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:72981314 G>A maps to NM_007332.2 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:87242047 C>G maps to NM_138817.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:87242047 C>G maps to NM_138817.2 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:90965507 G>A maps to NM_002485.4 F603F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:90965507 G>A maps to NM_002485.4 F603F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:92032431 G>A maps to NM_018710.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:92032431 G>A maps to NM_018710.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:103289201 G>A maps to NM_015902.4 F2169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:103289201 G>A maps to NM_015902.4 F2169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:110397820 T>A maps to ENST00000426474 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:110397820 T>A maps to ENST00000426474 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:113421232 C>T maps to NM_198123.1 Q1808Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:113421232 C>T maps to NM_198123.1 Q1808Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:143695305 G>C maps to NM_015193.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:143695305 G>C maps to NM_015193.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:146108150 C>T maps to NM_021061.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:146108150 C>T maps to NM_021061.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:69423575 G>C maps to NM_001098805.1 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:69423575 G>C maps to NM_001098805.1 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:71628519 G>A maps to NM_002732.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:71628519 G>A maps to NM_002732.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:74365159 G>A maps to NM_013390.2 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:74365159 G>A maps to NM_013390.2 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:75435902 C>T maps to NM_138691.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:75435902 C>T maps to NM_138691.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:91606128 G>A maps to NM_001001938.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:91606128 G>A maps to NM_001001938.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:114304422 C>G maps to NM_133464.2 S403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:114304422 C>G maps to NM_133464.2 S403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:114886645 G>A maps to NM_022486.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:114886645 G>A maps to NM_022486.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:115567234 G>A maps to NM_001012994.1 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:115567234 G>A maps to NM_001012994.1 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:128268676 C>T maps to NM_001006617.1 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:128268676 C>T maps to NM_001006617.1 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:138719359 G>A maps to ENST00000409386 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr9:138719359 G>A maps to ENST00000409386 F383F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chrX:1508131 A>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chrX:1508131 A>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chrX:6069471 C>T maps to ENST00000381093 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chrX:6069471 C>T maps to ENST00000381093 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chrX:69420190 C>A maps to NM_198512.1 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chrX:69420190 C>A maps to NM_198512.1 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chrX:102528930 C>G maps to NM_001012979.2 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chrX:102528930 C>G maps to NM_001012979.2 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chrX:103267304 G>A maps to NM_001002916.3 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chrX:103267304 G>A maps to NM_001002916.3 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chrX:117773417 C>G maps to ENST00000276204 S1341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chrX:117773417 C>G maps to ENST00000276204 S1341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chrX:148586601 G>A maps to NM_000202.5 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chrX:148586601 G>A maps to NM_000202.5 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr1:6880242 C>T maps to NM_015215.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr1:6880242 C>T maps to NM_015215.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr1:19992530 G>A maps to NM_000871.1 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr1:19992530 G>A maps to NM_000871.1 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr1:33235952 C>T maps to NM_020888.2 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr1:33235952 C>T maps to NM_020888.2 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr1:169529960 G>A maps to ENST00000367796 D139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr1:169529960 G>A maps to ENST00000367796 D139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr11:65298218 C>T maps to NM_020680.3 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr11:65298218 C>T maps to NM_020680.3 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr11:102987415 C>T maps to NM_001080463.1 R247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr11:102987415 C>T maps to NM_001080463.1 R247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr12:11420569 C>A maps to NM_006249.4 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr12:11420569 C>A maps to NM_006249.4 E205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr12:31586166 C>G maps to NM_144973.3 R676R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr12:31586166 C>G maps to NM_144973.3 R676R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr13:103441562 A>C maps to NM_024089.2 Y364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr13:103441562 A>C maps to NM_024089.2 Y364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr14:58605803 C>T maps to ENST00000438670 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr14:58605803 C>T maps to ENST00000438670 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr14:74968147 G>A maps to NM_000428.2 C1772C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr14:74968147 G>A maps to NM_000428.2 C1772C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr15:85447465 C>T maps to NM_004213.3 C200C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr15:85447465 C>T maps to NM_004213.3 C200C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr16:4432461 C>T maps to NM_138440.2 N528N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr16:4432461 C>T maps to NM_138440.2 N528N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr19:18968193 C>T maps to ENST00000418384 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr19:18968193 C>T maps to ENST00000418384 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr2:1652572 G>A maps to NM_012293.1 R993R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr2:1652572 G>A maps to NM_012293.1 R993R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr2:119739967 G>T maps to NM_006770.3 G349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr2:119739967 G>T maps to NM_006770.3 G349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr20:44641090 G>A maps to NM_004994.2 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr20:44641090 G>A maps to NM_004994.2 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr20:60900575 G>T maps to NM_005560.3 R1775R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr20:60900575 G>T maps to NM_005560.3 R1775R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr20:62421366 G>A maps to NM_025224.2 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr20:62421366 G>A maps to NM_025224.2 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr21:44837481 G>A maps to NM_173354.3 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr21:44837481 G>A maps to NM_173354.3 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr6:26157169 G>T maps to NM_005321.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr6:26157169 G>T maps to NM_005321.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr6:131917291 C>T maps to ENST00000403834 E936E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr6:131917291 C>T maps to ENST00000403834 E936E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr8:134474116 C>A did not map to a codon.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr8:134474116 C>A did not map to a codon.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr9:135273708 G>A maps to NM_007344.2 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr9:135273708 G>A maps to NM_007344.2 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr9:139995565 C>G maps to NM_016219.3 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4725-01A-01D-1434-08 chr9:139995565 C>G maps to NM_016219.3 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr1:151260749 G>A maps to NM_020832.1 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr1:151260749 G>A maps to NM_020832.1 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr1:228480266 C>T maps to NM_001098623.1 A3549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr1:228480266 C>T maps to NM_001098623.1 A3549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr11:56345152 T>C maps to NM_001004741.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr11:56345152 T>C maps to NM_001004741.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr11:56380882 A>C maps to NM_001004740.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr11:56380882 A>C maps to NM_001004740.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr11:56380888 T>C maps to NM_001004740.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr11:56380888 T>C maps to NM_001004740.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr11:62557443 G>A maps to NM_199337.2 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr11:62557443 G>A maps to NM_199337.2 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr12:13717096 G>A maps to NM_000834.3 I1025I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr12:13717096 G>A maps to NM_000834.3 I1025I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr12:49391989 C>T maps to NM_015086.1 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr12:49391989 C>T maps to NM_015086.1 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr14:36783736 A>G maps to NM_016586.2 N184N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr14:36783736 A>G maps to NM_016586.2 N184N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr15:85384097 C>A maps to NM_020778.4 R732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr15:85384097 C>A maps to NM_020778.4 R732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr16:30537132 G>A maps to NM_024671.3 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr16:30537132 G>A maps to NM_024671.3 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr16:77387770 C>A maps to NM_199355.2 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr16:77387770 C>A maps to NM_199355.2 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr17:7579309 A>T did not map to a codon.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr17:7579309 A>T did not map to a codon.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr17:33772743 G>C did not map to a codon.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr17:33772743 G>C did not map to a codon.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr17:36485439 G>A maps to ENST00000398597 Q1339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr17:36485439 G>A maps to ENST00000398597 Q1339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr17:66518979 C>A maps to NM_212472.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr17:66518979 C>A maps to NM_212472.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr18:20833899 C>T maps to NM_001100619.2 D587D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr18:20833899 C>T maps to NM_001100619.2 D587D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr18:21098935 C>T maps to NM_013326.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr18:21098935 C>T maps to NM_013326.3 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr19:13366019 C>A maps to NM_023035.2 P1552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr19:13366019 C>A maps to NM_023035.2 P1552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr19:44536828 C>G maps to NM_001129996.1 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr19:44536828 C>G maps to NM_001129996.1 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr2:3391501 C>T maps to NM_016030.5 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr2:3391501 C>T maps to NM_016030.5 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr2:27278586 C>T maps to NM_021831.5 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr2:27278586 C>T maps to NM_021831.5 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr2:49190546 G>T maps to NM_000145.3 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr2:49190546 G>T maps to NM_000145.3 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr2:80620388 T>C maps to ENST00000402739 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr2:80620388 T>C maps to ENST00000402739 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr2:105858866 G>T maps to NM_007227.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr2:105858866 G>T maps to NM_007227.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr5:90106532 T>C maps to NM_032119.3 P5152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr5:90106532 T>C maps to NM_032119.3 P5152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr5:140176609 G>T maps to NM_018905.2 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr5:140176609 G>T maps to NM_018905.2 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr6:26251970 A>G maps to NM_003524.2 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr6:26251970 A>G maps to NM_003524.2 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr7:132192726 G>T maps to NM_020911.1 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr7:132192726 G>T maps to NM_020911.1 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr7:143088774 G>T maps to NM_005232.4 Y930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr7:143088774 G>T maps to NM_005232.4 Y930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr8:141678370 C>T maps to NM_005607.4 V976V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr8:141678370 C>T maps to NM_005607.4 V976V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr8:141856356 A>G did not map to a codon.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chr8:141856356 A>G did not map to a codon.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chrX:125685919 C>T maps to NM_178470.4 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4726-01A-01D-1434-08 chrX:125685919 C>T maps to NM_178470.4 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:1267465 C>A maps to NM_152228.1 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:1267465 C>A maps to NM_152228.1 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:25254160 C>A maps to NM_001031680.2 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:25254160 C>A maps to NM_001031680.2 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:35350637 G>C maps to NM_001080418.1 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:35350637 G>C maps to NM_001080418.1 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:44685698 G>A maps to NM_019100.4 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:44685698 G>A maps to NM_019100.4 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:74833000 T>C maps to NM_001112808.2 C514C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:74833000 T>C maps to NM_001112808.2 C514C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:102312601 C>G did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:102312601 C>G did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:155851055 G>A maps to NM_152280.4 K351K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:155851055 G>A maps to NM_152280.4 K351K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:158582744 G>T maps to NM_003126.2 G2332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:158582744 G>T maps to NM_003126.2 G2332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:166974631 A>T maps to NM_032858.1 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:166974631 A>T maps to NM_032858.1 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:166987196 G>T did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:166987196 G>T did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:172357711 G>T did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:172357711 G>T did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:183177136 G>A maps to NM_005562.2 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:183177136 G>A maps to NM_005562.2 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:214170735 C>T maps to NM_002763.3 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:214170735 C>T maps to NM_002763.3 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:240964754 C>G maps to ENST00000407727 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:240964754 C>G maps to ENST00000407727 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:248636986 G>T maps to NM_001005495.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:248636986 G>T maps to NM_001005495.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:248737449 G>T maps to NM_001001821.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr1:248737449 G>T maps to NM_001001821.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:7773949 G>A maps to NM_002216.2 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:7773949 G>A maps to NM_002216.2 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:16955851 C>A maps to NM_001081.3 L2497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:16955851 C>A maps to NM_001081.3 L2497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:28030396 C>T maps to NM_173576.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:28030396 C>T maps to NM_173576.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:29762805 C>G maps to NM_021738.2 A1830A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:29762805 C>G maps to NM_021738.2 A1830A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:99215801 G>C did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:99215801 G>C did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:100219420 A>T maps to NM_021828.4 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:100219420 A>T maps to NM_021828.4 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:101658518 T>C did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:101658518 T>C did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:117486769 G>T maps to NM_207303.2 E1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr10:117486769 G>T maps to NM_207303.2 E1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:5291130 C>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:5291130 C>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:6220866 T>A maps to NM_001005178.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:6220866 T>A maps to NM_001005178.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:16071442 G>C maps to NM_001145819.1 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:16071442 G>C maps to NM_001145819.1 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:20673941 C>T maps to NM_004211.3 V726V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:20673941 C>T maps to NM_004211.3 V726V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:62437248 C>G maps to ENST00000431002 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:62437248 C>G maps to ENST00000431002 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:62751492 G>A maps to NM_004790.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:62751492 G>A maps to NM_004790.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:71942178 G>A maps to NM_001567.3 W481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:71942178 G>A maps to NM_001567.3 W481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:84996410 T>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr11:84996410 T>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:1995442 G>T maps to NM_172364.4 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:1995442 G>T maps to NM_172364.4 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:21375294 C>T maps to NM_006446.4 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:21375294 C>T maps to NM_006446.4 L582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:53045401 C>T maps to NM_000423.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:53045401 C>T maps to NM_000423.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:57974824 G>A maps to NM_004984.2 L875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:57974824 G>A maps to NM_004984.2 L875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:93873223 G>C maps to NM_172177.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:93873223 G>C maps to NM_172177.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:108051314 T>A maps to NM_001018072.1 Y1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:108051314 T>A maps to NM_001018072.1 Y1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:118198937 C>T maps to ENST00000339824 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:118198937 C>T maps to ENST00000339824 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:126138490 G>A maps to NM_052907.2 Q824Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr12:126138490 G>A maps to NM_052907.2 Q824Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr13:31233366 A>G maps to NM_005800.4 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr13:31233366 A>G maps to NM_005800.4 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr13:36700075 G>T maps to NM_004734.4 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr13:36700075 G>T maps to NM_004734.4 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr13:58208416 C>T maps to NM_001040429.2 N579N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr13:58208416 C>T maps to NM_001040429.2 N579N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:20928403 A>T maps to NM_001100814.1 C136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:20928403 A>T maps to NM_001100814.1 C136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:21831309 T>G did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:21831309 T>G did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:23567115 T>C maps to NM_017924.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:23567115 T>C maps to NM_017924.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:74371736 G>A maps to NM_021188.1 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:74371736 G>A maps to NM_021188.1 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:89041108 G>T maps to NM_024824.4 G312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:89041108 G>T maps to NM_024824.4 G312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:95080960 C>A maps to ENST00000393080 Y86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:95080960 C>A maps to ENST00000393080 Y86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:102453803 G>T maps to NM_001376.4 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:102453803 G>T maps to NM_001376.4 L851L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:104474747 A>C did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr14:104474747 A>C did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr15:22382672 C>A maps to NM_001005241.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr15:22382672 C>A maps to NM_001005241.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr15:25959217 G>A maps to NM_024490.3 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr15:25959217 G>A maps to NM_024490.3 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr15:37388488 C>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr15:37388488 C>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr15:54307971 C>T maps to ENST00000260323 Q958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr15:54307971 C>T maps to ENST00000260323 Q958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr15:76588078 C>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr15:76588078 C>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr15:83335613 C>A maps to NM_004644.3 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr15:83335613 C>A maps to NM_004644.3 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr15:97327403 A>G maps to NM_173499.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr15:97327403 A>G maps to NM_173499.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr16:632904 G>T maps to NM_148920.1 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr16:632904 G>T maps to NM_148920.1 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr16:72094423 C>A maps to NM_005143.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr16:72094423 C>A maps to NM_005143.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:4442814 C>G maps to NM_001105538.1 A1294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:4442814 C>G maps to NM_001105538.1 A1294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:11895760 C>T maps to NM_144680.2 W129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:11895760 C>T maps to NM_144680.2 W129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:47589373 G>A maps to NM_002507.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:47589373 G>A maps to NM_002507.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:62049719 G>A maps to NM_000334.4 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:62049719 G>A maps to NM_000334.4 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:62049988 G>T maps to NM_000334.4 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:62049988 G>T maps to NM_000334.4 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:70120398 C>A maps to NM_000346.3 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:70120398 C>A maps to NM_000346.3 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:77914882 G>A maps to NM_019020.2 F693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr17:77914882 G>A maps to NM_019020.2 F693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:5768220 C>G maps to NM_152784.3 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:5768220 C>G maps to NM_152784.3 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:6686811 G>A maps to NM_000064.2 A1197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:6686811 G>A maps to NM_000064.2 A1197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:15299971 G>A maps to NM_000435.2 C402C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:15299971 G>A maps to NM_000435.2 C402C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:15918352 G>A maps to NM_013940.2 H165H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:15918352 G>A maps to NM_013940.2 H165H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:16001225 C>T maps to NM_001082.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:16001225 C>T maps to NM_001082.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:22940816 G>A maps to ENST00000397104 Q541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:22940816 G>A maps to ENST00000397104 Q541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:41009735 G>T did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:41009735 G>T did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:46268860 C>A maps to NM_175875.4 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr19:46268860 C>A maps to NM_175875.4 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr2:1677463 G>A maps to NM_012293.1 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr2:1677463 G>A maps to NM_012293.1 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr2:11741111 C>T maps to NM_014668.3 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr2:11741111 C>T maps to NM_014668.3 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr2:12880595 C>T maps to NM_021643.3 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr2:12880595 C>T maps to NM_021643.3 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr2:58276055 A>T maps to NM_001130480.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr2:58276055 A>T maps to NM_001130480.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr2:115200369 C>A maps to NM_020868.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr2:115200369 C>A maps to NM_020868.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr2:138376010 C>T maps to ENST00000272643 V1208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr2:138376010 C>T maps to ENST00000272643 V1208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr2:212488769 C>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr2:212488769 C>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr20:1961151 G>A maps to NM_024411.4 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr20:1961151 G>A maps to NM_024411.4 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr20:39317052 C>A maps to NM_005461.3 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr20:39317052 C>A maps to NM_005461.3 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr20:57767408 C>A maps to NM_178457.1 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr20:57767408 C>A maps to NM_178457.1 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr21:28338239 C>A maps to NM_007038.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr21:28338239 C>A maps to NM_007038.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr21:30391544 C>T maps to NM_016940.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr21:30391544 C>T maps to NM_016940.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr21:32127483 G>T maps to NM_181619.1 C71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr21:32127483 G>T maps to NM_181619.1 C71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr22:17451083 C>G did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr22:17451083 C>G did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr22:19127504 G>A maps to NM_022719.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr22:19127504 G>A maps to NM_022719.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr22:32889194 G>C maps to NM_012179.3 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr22:32889194 G>C maps to NM_012179.3 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr3:32933212 G>A maps to NM_001039111.1 G839G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr3:32933212 G>A maps to NM_001039111.1 G839G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr3:74334567 G>C maps to NM_020872.1 A864A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr3:74334567 G>C maps to NM_020872.1 A864A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr3:99514874 C>A maps to ENST00000429802 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr3:99514874 C>A maps to ENST00000429802 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr3:127783718 G>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr3:127783718 G>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr3:130285859 C>A maps to NM_001102608.1 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr3:130285859 C>A maps to NM_001102608.1 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr3:169546665 G>T maps to NM_001080460.1 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr3:169546665 G>T maps to NM_001080460.1 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr3:170912382 C>G maps to NM_015028.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr3:170912382 C>G maps to NM_015028.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:25256887 G>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:25256887 G>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:25780750 G>A maps to NM_015187.3 Y844Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:25780750 G>A maps to NM_015187.3 Y844Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:145039885 G>T maps to NM_002099.6 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:145039885 G>T maps to NM_002099.6 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:155256094 T>A maps to NM_017639.3 K381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:155256094 T>A maps to NM_017639.3 K381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:169348296 A>G maps to NM_001012967.1 N618N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:169348296 A>G maps to NM_001012967.1 N618N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:175896750 C>T maps to NM_014269.4 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:175896750 C>T maps to NM_014269.4 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:178283594 G>T maps to NM_018248.2 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr4:178283594 G>T maps to NM_018248.2 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:1474682 C>A maps to NM_024830.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:1474682 C>A maps to NM_024830.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:13792156 A>G maps to NM_001369.2 S2798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:13792156 A>G maps to NM_001369.2 S2798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:38486047 G>A maps to NM_002310.5 D790D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:38486047 G>A maps to NM_002310.5 D790D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:39135035 C>T maps to ENST00000263405 K541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:39135035 C>T maps to ENST00000263405 K541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:80168933 G>T did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:80168933 G>T did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:101597727 G>T maps to NM_180991.4 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:101597727 G>T maps to NM_180991.4 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:131630516 C>A maps to NM_003059.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:131630516 C>A maps to NM_003059.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:140175844 G>A maps to NM_018905.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:140175844 G>A maps to NM_018905.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:140215374 G>T maps to NM_018910.2 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:140215374 G>T maps to NM_018910.2 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:140589726 G>A maps to NM_018932.3 E416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:140589726 G>A maps to NM_018932.3 E416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:140711621 C>A maps to NM_018912.2 Y457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:140711621 C>A maps to NM_018912.2 Y457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:158750295 C>A maps to NM_002187.2 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:158750295 C>A maps to NM_002187.2 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:176638274 G>T maps to NM_022455.4 G959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:176638274 G>T maps to NM_022455.4 G959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:29408400 C>A maps to NM_013941.2 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:29408400 C>A maps to NM_013941.2 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:32805815 C>G maps to ENST00000452392 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:32805815 C>G maps to ENST00000452392 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:97053871 C>A maps to NM_020482.4 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:97053871 C>A maps to NM_020482.4 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:97562023 C>A maps to NM_052904.3 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:97562023 C>A maps to NM_052904.3 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:106987307 G>A maps to NM_001624.2 Q1175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:106987307 G>A maps to NM_001624.2 Q1175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:134305617 G>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:134305617 G>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:146865141 C>G maps to NM_006834.3 Y45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:146865141 C>G maps to NM_006834.3 Y45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:155578188 C>G maps to ENST00000456144 V1709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr6:155578188 C>G maps to ENST00000456144 V1709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:6066484 C>A maps to NM_014413.3 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:6066484 C>A maps to NM_014413.3 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:38530703 C>G maps to NM_001635.3 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:38530703 C>G maps to NM_001635.3 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:44880521 C>A maps to ENST00000421098 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:44880521 C>A maps to ENST00000421098 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:47870816 G>C maps to NM_138295.3 Y2157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:47870816 G>C maps to NM_138295.3 Y2157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:75174441 C>T maps to NM_005338.4 W868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:75174441 C>T maps to NM_005338.4 W868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:81620520 A>T maps to NM_000722.2 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:81620520 A>T maps to NM_000722.2 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:93106954 A>G maps to NM_001164737.1 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:93106954 A>G maps to NM_001164737.1 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:93628606 C>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:93628606 C>A did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:158445167 C>T maps to NM_017760.5 K917K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr7:158445167 C>T maps to NM_017760.5 K917K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:54669196 C>A maps to NM_015941.2 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:54669196 C>A maps to NM_015941.2 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:110535589 C>T maps to ENST00000426474 Y4154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:110535589 C>T maps to ENST00000426474 Y4154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:117658758 G>C maps to ENST00000411422 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:117658758 G>C maps to ENST00000411422 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:121823956 C>A maps to NM_021021.3 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:121823956 C>A maps to NM_021021.3 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:144900182 T>G maps to NM_078480.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:144900182 T>G maps to NM_078480.1 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:144994358 C>G maps to NM_201380.2 L3347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:144994358 C>G maps to NM_201380.2 L3347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:145058521 C>A maps to NM_032789.3 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr8:145058521 C>A maps to NM_032789.3 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr9:84607716 G>T maps to NM_001001670.2 E778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr9:84607716 G>T maps to NM_001001670.2 E778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr9:90317990 G>T maps to NM_004938.2 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr9:90317990 G>T maps to NM_004938.2 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr9:101608272 G>A maps to NM_024642.3 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr9:101608272 G>A maps to NM_024642.3 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chrX:56296752 A>T maps to NM_007250.4 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chrX:56296752 A>T maps to NM_007250.4 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chrX:83128537 G>A maps to NM_021118.1 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chrX:83128537 G>A maps to NM_021118.1 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chrX:83351276 C>T maps to NM_014496.4 E632E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chrX:83351276 C>T maps to NM_014496.4 E632E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chrX:105855462 G>A maps to NM_018015.5 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chrX:105855462 G>A maps to NM_018015.5 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr1:37949127 G>C maps to NM_025079.2 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr1:37949127 G>C maps to NM_025079.2 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr1:66833699 T>C maps to NM_001037341.1 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr1:66833699 T>C maps to NM_001037341.1 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr1:151512817 G>A did not map to a codon.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr1:151512817 G>A did not map to a codon.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr10:71707079 C>T maps to ENST00000356340 P669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr10:71707079 C>T maps to ENST00000356340 P669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr10:94824175 G>A maps to NM_183374.2 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr10:94824175 G>A maps to NM_183374.2 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr10:102781635 G>A maps to NM_001195263.1 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr10:102781635 G>A maps to NM_001195263.1 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr11:14282158 A>T maps to NM_006108.2 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr11:14282158 A>T maps to NM_006108.2 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr11:69457890 C>T maps to NM_053056.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr11:69457890 C>T maps to NM_053056.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr12:56815187 C>A maps to NM_003920.3 E939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr12:56815187 C>A maps to NM_003920.3 E939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr12:57992918 C>T maps to NM_024779.4 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr12:57992918 C>T maps to NM_024779.4 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr12:83251022 C>A maps to NM_152588.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr12:83251022 C>A maps to NM_152588.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr12:120597954 C>T maps to NM_006836.1 R847R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr12:120597954 C>T maps to NM_006836.1 R847R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr13:50054402 C>T maps to NM_031915.2 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr13:50054402 C>T maps to NM_031915.2 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr14:77269771 G>A maps to NM_015305.3 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr14:77269771 G>A maps to NM_015305.3 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr15:74427050 C>T maps to NM_001130137.1 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr15:74427050 C>T maps to NM_001130137.1 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr17:12812248 G>C maps to NM_014859.4 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr17:12812248 G>C maps to NM_014859.4 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr17:46627998 C>T maps to NM_002146.4 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr17:46627998 C>T maps to NM_002146.4 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr17:65688859 C>T maps to NM_012417.2 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr17:65688859 C>T maps to NM_012417.2 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr19:1043250 G>A did not map to a codon.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr19:1043250 G>A did not map to a codon.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr19:16687956 C>T maps to NM_004831.3 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr19:16687956 C>T maps to NM_004831.3 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr19:45860922 T>C maps to NM_000400.3 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr19:45860922 T>C maps to NM_000400.3 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr19:57065935 C>T maps to NM_020828.1 C594C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr19:57065935 C>T maps to NM_020828.1 C594C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr19:58489923 G>A maps to NM_025027.3 Y708Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr19:58489923 G>A maps to NM_025027.3 Y708Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr2:25062773 T>A maps to NM_004036.3 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr2:25062773 T>A maps to NM_004036.3 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr2:99012565 C>T maps to NM_001298.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr2:99012565 C>T maps to NM_001298.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr2:209138377 G>T maps to NM_015040.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr2:209138377 G>T maps to NM_015040.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr2:219314034 C>G maps to NM_007127.2 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr2:219314034 C>G maps to NM_007127.2 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr20:10393769 G>C maps to NM_170784.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr20:10393769 G>C maps to NM_170784.1 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr20:10393970 G>C maps to NM_170784.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr20:10393970 G>C maps to NM_170784.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr20:43882276 C>T maps to NM_003064.2 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr20:43882276 C>T maps to NM_003064.2 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr3:44437945 C>T maps to NM_173826.3 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr3:44437945 C>T maps to NM_173826.3 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr3:44635867 G>A maps to NM_173658.1 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr3:44635867 G>A maps to NM_173658.1 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr3:48336721 C>T maps to NM_005793.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr3:48336721 C>T maps to NM_005793.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr3:108147436 G>A maps to NM_014981.1 L1222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr3:108147436 G>A maps to NM_014981.1 L1222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr3:167742807 G>A maps to NM_014498.3 Q567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr3:167742807 G>A maps to NM_014498.3 Q567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr3:184023707 C>G maps to NM_002808.3 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr3:184023707 C>G maps to NM_002808.3 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr4:85538788 C>T maps to NM_001263.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr4:85538788 C>T maps to NM_001263.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr5:63257048 G>A maps to NM_000524.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr5:63257048 G>A maps to NM_000524.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr6:56505115 G>C maps to ENST00000361203 S561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr6:56505115 G>C maps to ENST00000361203 S561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr6:152469387 A>G maps to NM_182961.2 N8256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr6:152469387 A>G maps to NM_182961.2 N8256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr6:165715309 G>A maps to NM_144980.3 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr6:165715309 G>A maps to NM_144980.3 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr7:157160130 C>T maps to NM_058246.3 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr7:157160130 C>T maps to NM_058246.3 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr8:59409509 G>A maps to NM_000780.3 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr8:59409509 G>A maps to NM_000780.3 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr8:125076787 G>T maps to NM_001039112.2 E1177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr8:125076787 G>T maps to NM_001039112.2 E1177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr8:125498930 G>A maps to NM_007218.3 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr8:125498930 G>A maps to NM_007218.3 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr9:138714637 G>A maps to ENST00000409386 I634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chr9:138714637 G>A maps to ENST00000409386 I634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chrX:78217000 C>T maps to NM_198333.1 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chrX:78217000 C>T maps to NM_198333.1 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chrX:118604390 G>A maps to NM_001152.4 Q218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4728-01A-01D-1434-08 chrX:118604390 G>A maps to NM_001152.4 Q218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr1:21928277 C>T maps to NM_001145658.1 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr1:21928277 C>T maps to NM_001145658.1 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr1:29475407 C>T maps to NM_005626.4 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr1:29475407 C>T maps to NM_005626.4 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr1:247608111 G>C maps to NM_004895.4 L1000L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr1:247608111 G>C maps to NM_004895.4 L1000L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr1:249142663 C>T maps to NM_024836.1 C397C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr1:249142663 C>T maps to NM_024836.1 C397C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:4409646 C>T maps to NM_003141.3 E206E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:4409646 C>T maps to NM_003141.3 E206E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:57261526 G>A maps to NM_003627.5 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:57261526 G>A maps to NM_003627.5 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:64893284 C>A maps to NM_004927.3 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:64893284 C>A maps to NM_004927.3 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:92534059 C>T maps to ENST00000298047 P2627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:92534059 C>T maps to ENST00000298047 P2627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:99690440 G>A maps to NM_014361.2 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:99690440 G>A maps to NM_014361.2 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:114392968 G>A maps to ENST00000424269 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:114392968 G>A maps to ENST00000424269 I455I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:125301234 C>T maps to NM_022062.2 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr11:125301234 C>T maps to NM_022062.2 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr12:247992 C>T maps to NM_001170738.1 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr12:247992 C>T maps to NM_001170738.1 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr12:2659196 G>T maps to NM_199460.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr12:2659196 G>T maps to NM_199460.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr13:58207105 G>A maps to NM_001040429.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr13:58207105 G>A maps to NM_001040429.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr14:52194512 C>T maps to ENST00000344768 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr14:52194512 C>T maps to ENST00000344768 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr15:65114582 C>T maps to ENST00000333425 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr15:65114582 C>T maps to ENST00000333425 G233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr15:74707065 C>T maps to NM_003612.3 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr15:74707065 C>T maps to NM_003612.3 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr15:79231499 G>A maps to NM_004390.3 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr15:79231499 G>A maps to NM_004390.3 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr15:90229777 C>G did not map to a codon.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr15:90229777 C>G did not map to a codon.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr16:28856349 G>A maps to NM_003321.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr16:28856349 G>A maps to NM_003321.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr16:57088720 C>T maps to NM_032206.3 L1189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr16:57088720 C>T maps to NM_032206.3 L1189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr16:58030906 G>A maps to NM_020807.1 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr16:58030906 G>A maps to NM_020807.1 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr17:6939687 C>A did not map to a codon.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr17:6939687 C>A did not map to a codon.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr17:7604803 G>T maps to NM_018081.2 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr17:7604803 G>T maps to NM_018081.2 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr17:8049768 G>A maps to NM_002616.2 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr17:8049768 G>A maps to NM_002616.2 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr17:78321812 C>T maps to NM_020914.4 C3275C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr17:78321812 C>T maps to NM_020914.4 C3275C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr18:72999254 G>A maps to NM_005786.4 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr18:72999254 G>A maps to NM_005786.4 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr19:36883702 C>T maps to NM_133466.2 K513K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr19:36883702 C>T maps to NM_133466.2 K513K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr2:29249762 C>G maps to NM_199280.2 S633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr2:29249762 C>G maps to NM_199280.2 S633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr2:96690175 G>A maps to NM_207328.2 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr2:96690175 G>A maps to NM_207328.2 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr2:141533691 T>C maps to NM_018557.2 K1825K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr2:141533691 T>C maps to NM_018557.2 K1825K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr2:171573746 C>T maps to NM_001003845.2 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr2:171573746 C>T maps to NM_001003845.2 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr2:212589878 G>A maps to NM_005235.2 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr2:212589878 G>A maps to NM_005235.2 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr2:242277150 C>T maps to ENST00000391972 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr2:242277150 C>T maps to ENST00000391972 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr20:398253 C>G maps to NM_031229.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr20:398253 C>G maps to NM_031229.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr22:20127355 C>T maps to NM_013373.3 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr22:20127355 C>T maps to NM_013373.3 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr22:24135758 G>T maps to NM_003073.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr22:24135758 G>T maps to NM_003073.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr22:37770533 C>T maps to NM_052906.3 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr22:37770533 C>T maps to NM_052906.3 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr22:41623202 C>T maps to NM_031488.4 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr22:41623202 C>T maps to NM_031488.4 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr3:97806282 C>T maps to NM_054106.1 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr3:97806282 C>T maps to NM_054106.1 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr3:124515328 G>A maps to NM_002213.3 C533C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr3:124515328 G>A maps to NM_002213.3 C533C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr3:147108848 C>T maps to NM_001168379.1 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr3:147108848 C>T maps to NM_001168379.1 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr3:151105632 G>A maps to NM_053002.4 P1673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr3:151105632 G>A maps to NM_053002.4 P1673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr3:190362142 C>T maps to NM_002182.3 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr3:190362142 C>T maps to NM_002182.3 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr3:196198800 C>T maps to NM_152617.3 K535K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr3:196198800 C>T maps to NM_152617.3 K535K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr4:26422342 T>C maps to NM_005349.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr4:26422342 T>C maps to NM_005349.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr4:103949912 G>A maps to NM_178833.4 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr4:103949912 G>A maps to NM_178833.4 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr5:9108254 A>G maps to NM_003966.2 N690N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr5:9108254 A>G maps to NM_003966.2 N690N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr5:10414542 A>T did not map to a codon.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr5:10414542 A>T did not map to a codon.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr5:52347332 G>A maps to NM_002203.3 Q241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr5:52347332 G>A maps to NM_002203.3 Q241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr5:169031116 C>G maps to NM_017785.4 S575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr5:169031116 C>G maps to NM_017785.4 S575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr6:18207750 C>T maps to ENST00000388870 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr6:18207750 C>T maps to ENST00000388870 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr7:98248962 C>G maps to NM_002523.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr7:98248962 C>G maps to NM_002523.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr8:35608197 C>A maps to ENST00000416672 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr8:35608197 C>A maps to ENST00000416672 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr8:139180195 G>T maps to NM_015912.3 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr8:139180195 G>T maps to NM_015912.3 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr9:111745496 C>T maps to NM_003798.2 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr9:111745496 C>T maps to NM_003798.2 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chrX:18234752 T>A maps to NM_153346.4 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chrX:18234752 T>A maps to NM_153346.4 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr1:26349619 C>T maps to NM_004455.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr1:26349619 C>T maps to NM_004455.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr1:63789385 G>A maps to NM_012183.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr1:63789385 G>A maps to NM_012183.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr1:75037805 C>T maps to NM_001002912.4 L1196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr1:75037805 C>T maps to NM_001002912.4 L1196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr1:226127191 C>T maps to NM_003240.3 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr1:226127191 C>T maps to NM_003240.3 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr1:237829846 G>T maps to NM_001035.2 R2824R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr1:237829846 G>T maps to NM_001035.2 R2824R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr10:30749692 C>T maps to NM_005204.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr10:30749692 C>T maps to NM_005204.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr10:131640455 C>T maps to ENST00000355311 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr10:131640455 C>T maps to ENST00000355311 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr10:134004264 G>A maps to NM_006426.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr10:134004264 G>A maps to NM_006426.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr11:60234504 G>A maps to NM_152866.2 W216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr11:60234504 G>A maps to NM_152866.2 W216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr11:64519901 G>A maps to NM_005609.2 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr11:64519901 G>A maps to NM_005609.2 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr11:94038882 C>T maps to NM_001080486.1 C27C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr11:94038882 C>T maps to NM_001080486.1 C27C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr12:5021956 C>G maps to NM_000217.2 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr12:5021956 C>G maps to NM_000217.2 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr12:50500209 G>C did not map to a codon.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr12:50500209 G>C did not map to a codon.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr14:20692281 T>A maps to NM_001004480.1 Y138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr14:20692281 T>A maps to NM_001004480.1 Y138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr16:4519401 C>T maps to NM_020677.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr16:4519401 C>T maps to NM_020677.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr16:30122797 C>T maps to NM_024307.2 W206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr16:30122797 C>T maps to NM_024307.2 W206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr16:55846956 T>A did not map to a codon.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr16:55846956 T>A did not map to a codon.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr17:27837970 G>A maps to NM_020791.2 Q555Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr17:27837970 G>A maps to NM_020791.2 Q555Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr17:61901557 G>C maps to NM_017647.3 S347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr17:61901557 G>C maps to NM_017647.3 S347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr17:61902697 G>A maps to NM_017647.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr17:61902697 G>A maps to NM_017647.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr18:7231915 C>T maps to NM_001105581.1 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr18:7231915 C>T maps to NM_001105581.1 I260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr19:9271902 A>T maps to NM_020933.4 K528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr19:9271902 A>T maps to NM_020933.4 K528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr19:22363090 A>G maps to NM_001001411.2 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr19:22363090 A>G maps to NM_001001411.2 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr2:31483526 G>C maps to NM_014600.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr2:31483526 G>C maps to NM_014600.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr2:170103910 G>T maps to NM_004525.2 S962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr2:170103910 G>T maps to NM_004525.2 S962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr2:175742726 T>A maps to NM_001822.4 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr2:175742726 T>A maps to NM_001822.4 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr2:202050585 C>G maps to NM_032977.3 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr2:202050585 C>G maps to NM_032977.3 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr20:42694518 G>A maps to ENST00000348077 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr20:42694518 G>A maps to ENST00000348077 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr21:30315990 G>C maps to NM_015565.2 Y1452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr21:30315990 G>C maps to NM_015565.2 Y1452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr3:47037918 C>T maps to NM_015175.1 S770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr3:47037918 C>T maps to NM_015175.1 S770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr3:111688637 A>G maps to NM_001134438.1 V1139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr3:111688637 A>G maps to NM_001134438.1 V1139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr3:119396194 A>T did not map to a codon.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr3:119396194 A>T did not map to a codon.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr3:154018466 T>C maps to NM_020865.2 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr3:154018466 T>C maps to NM_020865.2 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr3:189349234 A>G did not map to a codon.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr3:189349234 A>G did not map to a codon.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr4:37633099 C>T maps to NM_001085399.1 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr4:37633099 C>T maps to NM_001085399.1 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr4:57843127 C>G maps to NM_032313.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr4:57843127 C>G maps to NM_032313.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr4:96091408 G>A maps to NM_003728.3 F842F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr4:96091408 G>A maps to NM_003728.3 F842F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr4:153250882 G>A maps to NM_033632.2 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr4:153250882 G>A maps to NM_033632.2 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr5:139060914 C>T maps to NM_016463.7 C269C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr5:139060914 C>T maps to NM_016463.7 C269C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr5:141019627 G>C maps to NM_173828.4 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr5:141019627 G>C maps to NM_173828.4 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr6:41773476 G>C maps to ENST00000373009 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr6:41773476 G>C maps to ENST00000373009 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr7:158529771 G>C maps to NM_020728.2 S816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr7:158529771 G>C maps to NM_020728.2 S816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:56015392 C>T maps to NM_052898.1 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:56015392 C>T maps to NM_052898.1 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:67796028 C>T maps to NM_173518.4 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:67796028 C>T maps to NM_173518.4 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:88885611 C>T maps to NM_152418.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:88885611 C>T maps to NM_152418.3 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:100115241 C>G maps to NM_017890.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:100115241 C>G maps to NM_017890.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:144993497 C>T maps to NM_201380.2 E3634E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:144993497 C>T maps to NM_201380.2 E3634E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:144995837 C>T maps to NM_201380.2 Q2854Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:144995837 C>T maps to NM_201380.2 Q2854Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:144997460 C>T maps to NM_201380.2 L2349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:144997460 C>T maps to NM_201380.2 L2349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:144997544 C>T maps to NM_201380.2 V2321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:144997544 C>T maps to NM_201380.2 V2321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:144997568 C>T maps to NM_201380.2 Q2313Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:144997568 C>T maps to NM_201380.2 Q2313Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:144998345 C>G maps to NM_201380.2 L2054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:144998345 C>G maps to NM_201380.2 L2054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:144998528 G>A maps to NM_201380.2 L1993L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr8:144998528 G>A maps to NM_201380.2 L1993L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr9:20346500 C>A maps to NM_004529.2 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr9:20346500 C>A maps to NM_004529.2 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr9:131260796 G>A maps to NM_153435.1 R770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4730-01A-01D-1434-08 chr9:131260796 G>A maps to NM_153435.1 R770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr1:891547 T>A maps to NM_015658.3 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr1:891547 T>A maps to NM_015658.3 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr1:155240699 C>T maps to ENST00000368361 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr1:155240699 C>T maps to ENST00000368361 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr1:248059226 G>T maps to NM_001001957.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr1:248059226 G>T maps to NM_001001957.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr10:53459123 G>A maps to NM_015235.2 C62C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr10:53459123 G>A maps to NM_015235.2 C62C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr10:70531027 A>G maps to NM_018237.2 K788K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr10:70531027 A>G maps to NM_018237.2 K788K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr10:95995856 G>A maps to ENST00000371380 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr10:95995856 G>A maps to ENST00000371380 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr11:56043908 G>C maps to NM_001004745.1 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr11:56043908 G>C maps to NM_001004745.1 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr11:61042027 G>C maps to NM_152718.2 Y508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr11:61042027 G>C maps to NM_152718.2 Y508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr11:69062838 C>A maps to NM_138768.2 C6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr11:69062838 C>A maps to NM_138768.2 C6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr12:49435774 T>C did not map to a codon.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr12:49435774 T>C did not map to a codon.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr12:52201176 C>T maps to NM_014191.2 A1969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr12:52201176 C>T maps to NM_014191.2 A1969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr12:52378995 C>T maps to NM_020328.3 R375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr12:52378995 C>T maps to NM_020328.3 R375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr12:57571368 C>T maps to NM_002332.2 D1452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr12:57571368 C>T maps to NM_002332.2 D1452D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr14:50736049 T>G did not map to a codon.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr14:50736049 T>G did not map to a codon.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr14:95033333 C>G maps to NM_006215.2 S226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr14:95033333 C>G maps to NM_006215.2 S226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr16:29923280 C>T maps to NM_178863.2 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr16:29923280 C>T maps to NM_178863.2 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr16:31332572 C>A maps to NM_001145808.1 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr16:31332572 C>A maps to NM_001145808.1 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr16:53639438 G>A maps to NM_015272.2 A1263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr16:53639438 G>A maps to NM_015272.2 A1263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr16:78133747 A>T maps to NM_016373.1 R25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr16:78133747 A>T maps to NM_016373.1 R25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr16:89257809 C>T maps to NM_004933.2 H435H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr16:89257809 C>T maps to NM_004933.2 H435H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr17:7415499 C>T maps to NM_000937.4 A1443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr17:7415499 C>T maps to NM_000937.4 A1443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr17:7578418 C>A maps to NM_001126112.1 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr17:7578418 C>A maps to NM_001126112.1 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr17:7734484 C>T maps to NM_020877.2 G4104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr17:7734484 C>T maps to NM_020877.2 G4104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr17:17079759 A>G maps to NM_015134.2 E910E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr17:17079759 A>G maps to NM_015134.2 E910E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr17:27075533 C>T maps to NM_004295.3 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr17:27075533 C>T maps to NM_004295.3 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr17:59115301 C>A maps to ENST00000407086 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr17:59115301 C>A maps to ENST00000407086 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr19:11363490 G>A maps to ENST00000319867 C92C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr19:11363490 G>A maps to ENST00000319867 C92C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr19:17412026 G>A maps to NM_024527.4 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr19:17412026 G>A maps to NM_024527.4 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr19:37038094 A>G maps to NM_001145649.1 C455C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr19:37038094 A>G maps to NM_001145649.1 C455C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr19:55087421 G>T maps to NM_001130917.1 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr19:55087421 G>T maps to NM_001130917.1 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr2:26717899 C>T maps to NM_194248.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr2:26717899 C>T maps to NM_194248.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr2:120128363 G>A maps to NM_001178017.1 W120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr2:120128363 G>A maps to NM_001178017.1 W120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr2:136418926 C>T maps to ENST00000409606 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr2:136418926 C>T maps to ENST00000409606 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr20:25262776 C>A maps to NM_002862.3 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr20:25262776 C>A maps to NM_002862.3 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr20:30497541 G>T maps to NM_001008409.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr20:30497541 G>T maps to NM_001008409.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr20:43726836 C>T maps to NM_002251.3 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr20:43726836 C>T maps to NM_002251.3 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr22:34046370 C>A maps to NM_133642.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr22:34046370 C>A maps to NM_133642.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr3:45636952 A>G maps to NM_014240.2 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr3:45636952 A>G maps to NM_014240.2 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr3:122287598 T>A maps to NM_138287.3 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr3:122287598 T>A maps to NM_138287.3 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr3:160395541 C>T maps to NM_025047.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr3:160395541 C>T maps to NM_025047.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr3:173993198 C>T maps to NM_014932.2 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr3:173993198 C>T maps to NM_014932.2 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr4:7056306 C>G maps to NM_152293.2 Y263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr4:7056306 C>G maps to NM_152293.2 Y263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr4:41749527 G>A maps to NM_003924.3 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr4:41749527 G>A maps to NM_003924.3 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr4:114264271 G>T maps to NM_001148.4 E1408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr4:114264271 G>T maps to NM_001148.4 E1408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr4:123305080 A>G maps to NM_139243.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr4:123305080 A>G maps to NM_139243.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr5:801278 C>T maps to NM_024786.2 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr5:801278 C>T maps to NM_024786.2 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr5:16616783 G>A maps to NM_001034850.1 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr5:16616783 G>A maps to NM_001034850.1 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr5:33576200 G>A maps to NM_030955.2 N1310N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr5:33576200 G>A maps to NM_030955.2 N1310N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr6:26056368 C>G maps to NM_005319.3 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr6:26056368 C>G maps to NM_005319.3 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr6:54254653 A>G maps to NM_014464.3 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr6:54254653 A>G maps to NM_014464.3 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr6:56394428 C>T maps to ENST00000361203 E5593E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr6:56394428 C>T maps to ENST00000361203 E5593E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr6:129674410 C>T maps to NM_000426.3 V1542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr6:129674410 C>T maps to NM_000426.3 V1542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr7:142836665 T>G maps to NM_002652.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr7:142836665 T>G maps to NM_002652.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr8:55539812 C>A maps to NM_006269.1 S1124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr8:55539812 C>A maps to NM_006269.1 S1124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr8:100533239 T>A did not map to a codon.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr8:100533239 T>A did not map to a codon.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr8:118552147 G>A maps to NM_080651.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chr8:118552147 G>A maps to NM_080651.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chrX:152956768 C>T maps to NM_005629.3 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4731-01A-01D-1434-08 chrX:152956768 C>T maps to NM_005629.3 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr1:12819313 C>T maps to NM_152290.2 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr1:12819313 C>T maps to NM_152290.2 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr1:19166790 G>A maps to NM_152232.2 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr1:19166790 G>A maps to NM_152232.2 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr1:27089710 C>T maps to NM_006015.4 G889G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr1:27089710 C>T maps to NM_006015.4 G889G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr12:100784776 A>G did not map to a codon.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr12:100784776 A>G did not map to a codon.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr14:23884263 G>A maps to NM_000257.2 N1833N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr14:23884263 G>A maps to NM_000257.2 N1833N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr14:64656946 C>T maps to NM_182914.2 I6010I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr14:64656946 C>T maps to NM_182914.2 I6010I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr15:91433124 C>T maps to NM_002005.3 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr15:91433124 C>T maps to NM_002005.3 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr16:15718916 C>T maps to NM_014647.3 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr16:15718916 C>T maps to NM_014647.3 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr16:71898870 T>A maps to ENST00000425432 K83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr16:71898870 T>A maps to ENST00000425432 K83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr17:40716510 C>G maps to NM_001042532.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr17:40716510 C>G maps to NM_001042532.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr17:46847447 G>A maps to NM_001130918.1 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr17:46847447 G>A maps to NM_001130918.1 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr17:63554318 C>T maps to NM_004655.3 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr17:63554318 C>T maps to NM_004655.3 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr22:19028790 G>A maps to NM_005137.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr22:19028790 G>A maps to NM_005137.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr4:114290864 G>A maps to NM_001148.4 E3838E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr4:114290864 G>A maps to NM_001148.4 E3838E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr4:126241840 T>C maps to NM_024582.4 I1425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr4:126241840 T>C maps to NM_024582.4 I1425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr6:46661018 G>A maps to NM_001010870.2 Q1718Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4733-01A-02D-1870-08 chr6:46661018 G>A maps to NM_001010870.2 Q1718Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr1:11728955 C>T maps to NM_018438.5 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr1:11728955 C>T maps to NM_018438.5 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr1:12251957 G>A maps to NM_001066.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr1:12251957 G>A maps to NM_001066.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr1:16464403 G>C maps to NM_004431.3 S419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr1:16464403 G>C maps to NM_004431.3 S419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr1:55089014 G>T maps to NM_176782.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr1:55089014 G>T maps to NM_176782.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr1:154898893 C>T maps to NM_006556.3 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr1:154898893 C>T maps to NM_006556.3 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr1:155057800 G>A maps to ENST00000505139 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr1:155057800 G>A maps to ENST00000505139 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr1:158650471 G>A maps to NM_003126.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr1:158650471 G>A maps to NM_003126.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr10:128974487 C>A maps to NM_001039762.2 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr10:128974487 C>A maps to NM_001039762.2 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr11:58034970 C>T maps to NM_207374.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr11:58034970 C>T maps to NM_207374.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr12:5941700 C>T maps to ENST00000356134 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr12:5941700 C>T maps to ENST00000356134 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr12:6659914 C>T maps to NM_001193457.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr12:6659914 C>T maps to NM_001193457.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr12:8374609 G>A maps to NM_018088.3 N401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr12:8374609 G>A maps to NM_018088.3 N401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr12:81101863 C>T maps to NM_002469.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr12:81101863 C>T maps to NM_002469.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr12:88589181 C>G maps to NM_181783.3 S834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr12:88589181 C>G maps to NM_181783.3 S834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr12:95927269 G>A maps to NM_032147.2 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr12:95927269 G>A maps to NM_032147.2 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr12:116457050 G>A maps to NM_015335.4 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr12:116457050 G>A maps to NM_015335.4 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr13:43180975 G>A maps to NM_003701.3 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr13:43180975 G>A maps to NM_003701.3 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr14:90770701 G>A maps to NM_017970.2 C194C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr14:90770701 G>A maps to NM_017970.2 C194C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr14:100119153 C>T maps to NM_001127258.1 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr14:100119153 C>T maps to NM_001127258.1 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr14:102509075 G>A maps to NM_001376.4 R4168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr14:102509075 G>A maps to NM_001376.4 R4168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr15:30018666 A>G maps to NM_003257.3 N776N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr15:30018666 A>G maps to NM_003257.3 N776N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr15:78454628 G>A maps to NM_005530.2 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr15:78454628 G>A maps to NM_005530.2 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr16:31404707 G>A maps to ENST00000444228 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr16:31404707 G>A maps to ENST00000444228 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr16:47694702 C>G maps to NM_000293.2 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr16:47694702 C>G maps to NM_000293.2 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr16:56878442 C>G maps to NM_014669.3 T794T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr16:56878442 C>G maps to NM_014669.3 T794T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr16:69681024 C>T maps to NM_138713.2 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr16:69681024 C>T maps to NM_138713.2 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr17:3658513 G>T maps to NM_002208.4 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr17:3658513 G>T maps to NM_002208.4 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr17:7329024 G>A maps to NM_175734.4 W6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr17:7329024 G>A maps to NM_175734.4 W6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr17:27889908 G>A maps to NM_198147.2 D359D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr17:27889908 G>A maps to NM_198147.2 D359D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr17:39019388 G>A maps to NM_000223.3 D434D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr17:39019388 G>A maps to NM_000223.3 D434D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr17:40842781 G>A maps to NM_003632.2 R627R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr17:40842781 G>A maps to NM_003632.2 R627R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr17:78182029 C>T maps to NM_024110.2 Y967Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr17:78182029 C>T maps to NM_024110.2 Y967Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr18:22805214 G>A maps to NM_015461.2 D889D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr18:22805214 G>A maps to NM_015461.2 D889D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr18:59888729 G>A maps to NM_020854.3 Q286Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr18:59888729 G>A maps to NM_020854.3 Q286Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr19:9226034 G>A maps to ENST00000293614 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr19:9226034 G>A maps to ENST00000293614 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr19:15918181 G>A maps to NM_013940.2 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr19:15918181 G>A maps to NM_013940.2 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr19:18254653 G>A maps to NM_015016.1 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr19:18254653 G>A maps to NM_015016.1 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr19:19230816 G>A maps to NM_017814.1 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr19:19230816 G>A maps to NM_017814.1 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr19:43530464 G>C maps to ENST00000306308 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr19:43530464 G>C maps to ENST00000306308 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr19:44341278 G>A maps to NM_181845.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr19:44341278 G>A maps to NM_181845.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr2:25467434 G>A maps to NM_175629.1 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr2:25467434 G>A maps to NM_175629.1 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr2:97526458 G>A maps to NM_017789.4 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr2:97526458 G>A maps to NM_017789.4 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr2:202151269 C>T maps to NM_001080125.1 Q524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr2:202151269 C>T maps to NM_001080125.1 Q524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr2:220081143 C>T maps to NM_005689.2 W304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr2:220081143 C>T maps to NM_005689.2 W304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr20:31812909 C>T maps to NM_178466.3 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr20:31812909 C>T maps to NM_178466.3 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr20:44515722 C>T maps to NM_080608.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr20:44515722 C>T maps to NM_080608.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr21:10951320 G>A maps to NM_199261.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr21:10951320 G>A maps to NM_199261.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr22:30812007 C>T maps to NM_012429.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr22:30812007 C>T maps to NM_012429.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr22:36960637 C>A maps to NM_006078.3 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr22:36960637 C>A maps to NM_006078.3 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr3:9828793 C>T did not map to a codon.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr3:9828793 C>T did not map to a codon.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr3:53844074 G>A maps to NM_001128840.1 W1981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr3:53844074 G>A maps to NM_001128840.1 W1981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr3:111688637 A>G maps to NM_001134438.1 V1139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr3:111688637 A>G maps to NM_001134438.1 V1139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr4:89583678 C>G maps to NM_014606.1 S415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr4:89583678 C>G maps to NM_014606.1 S415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr4:119059258 G>T maps to NM_004784.2 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr4:119059258 G>T maps to NM_004784.2 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr4:185311903 C>G did not map to a codon.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr4:185311903 C>G did not map to a codon.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr5:36986386 A>G maps to NM_133433.3 P1035P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr5:36986386 A>G maps to NM_133433.3 P1035P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr5:137802444 G>C did not map to a codon.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr5:137802444 G>C did not map to a codon.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr5:147796564 T>G maps to NM_205836.1 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr5:147796564 T>G maps to NM_205836.1 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr5:156895763 C>T maps to NM_001099287.1 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr5:156895763 C>T maps to NM_001099287.1 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr6:26156773 G>A maps to NM_005321.2 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr6:26156773 G>A maps to NM_005321.2 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr6:56443678 C>T maps to ENST00000361203 T4109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr6:56443678 C>T maps to ENST00000361203 T4109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr7:21469032 C>T maps to NM_003112.3 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr7:21469032 C>T maps to NM_003112.3 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr7:44185250 G>A maps to NM_000162.3 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr7:44185250 G>A maps to NM_000162.3 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr7:44924865 C>A maps to NM_033224.3 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr7:44924865 C>A maps to NM_033224.3 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr7:99917322 G>A maps to NM_001004351.4 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr7:99917322 G>A maps to NM_001004351.4 P494P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CN-4734-01A-01D-1434-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-CN-4734-01A-01D-1434-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr7:122033248 C>T did not map to a codon.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr7:122033248 C>T did not map to a codon.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr7:141672667 G>A maps to NM_176817.4 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr7:141672667 G>A maps to NM_176817.4 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr8:119938850 G>A maps to NM_002546.3 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr8:119938850 G>A maps to NM_002546.3 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr8:133144492 G>C maps to NM_004519.2 A606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr8:133144492 G>C maps to NM_004519.2 A606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr9:2039805 G>A maps to NM_003070.3 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr9:2039805 G>A maps to NM_003070.3 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr9:22451197 C>G maps to NM_022160.2 S268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr9:22451197 C>G maps to NM_022160.2 S268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr9:139701273 C>T maps to NM_001039374.4 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4734-01A-01D-1434-08 chr9:139701273 C>T maps to NM_001039374.4 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr1:21808092 C>A maps to NM_032264.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr1:21808092 C>A maps to NM_032264.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr1:22313043 C>T maps to NM_007352.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr1:22313043 C>T maps to NM_007352.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr1:68153399 C>T maps to NM_001924.3 C147C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr1:68153399 C>T maps to NM_001924.3 C147C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr1:90049933 G>T maps to NM_015350.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr1:90049933 G>T maps to NM_015350.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr1:149879360 T>C maps to NM_014849.3 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr1:149879360 T>C maps to NM_014849.3 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr1:198721487 G>A maps to ENST00000271610 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr1:198721487 G>A maps to ENST00000271610 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr10:46322370 G>A maps to ENST00000355953 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr10:46322370 G>A maps to ENST00000355953 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr10:72324151 G>A maps to NM_014431.2 R765R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr10:72324151 G>A maps to NM_014431.2 R765R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr11:1858220 G>A maps to NM_138567.3 Q289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr11:1858220 G>A maps to NM_138567.3 Q289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr11:56344939 G>A maps to NM_001004741.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr11:56344939 G>A maps to NM_001004741.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr11:71906661 C>T maps to NM_016729.2 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr11:71906661 C>T maps to NM_016729.2 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr11:88911534 C>T maps to NM_000372.4 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr11:88911534 C>T maps to NM_000372.4 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr12:49445125 G>T maps to NM_003482.3 C780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr12:49445125 G>T maps to NM_003482.3 C780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr12:58018674 C>A maps to NM_133489.2 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr12:58018674 C>A maps to NM_133489.2 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr12:130184677 G>A maps to NM_133448.2 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr12:130184677 G>A maps to NM_133448.2 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr14:24808259 C>T maps to NM_006871.3 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr14:24808259 C>T maps to NM_006871.3 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr14:39716524 C>T maps to NM_054024.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr14:39716524 C>T maps to NM_054024.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr14:52781580 G>A maps to NM_000956.3 E105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr14:52781580 G>A maps to NM_000956.3 E105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr14:73959251 C>T maps to NM_024644.2 C510C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr14:73959251 C>T maps to NM_024644.2 C510C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr15:33359986 G>A maps to NM_001103184.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr15:33359986 G>A maps to NM_001103184.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr16:2376443 C>T maps to NM_001089.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr16:2376443 C>T maps to NM_001089.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr16:52497887 G>A maps to ENST00000407228 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr16:52497887 G>A maps to ENST00000407228 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr17:39522832 G>A maps to ENST00000394004 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr17:39522832 G>A maps to ENST00000394004 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr17:73915955 C>T did not map to a codon.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr17:73915955 C>T did not map to a codon.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr17:76167594 C>T maps to NM_004710.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr17:76167594 C>T maps to NM_004710.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr18:70461639 C>G did not map to a codon.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr18:70461639 C>G did not map to a codon.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr18:71797838 C>T maps to NM_001142958.1 W129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr18:71797838 C>T maps to NM_001142958.1 W129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:4817883 G>T maps to NM_182919.2 S169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:4817883 G>T maps to NM_182919.2 S169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:11283761 G>A maps to NM_015493.6 Y710Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:11283761 G>A maps to NM_015493.6 Y710Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:12976158 C>T maps to NM_014975.2 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:12976158 C>T maps to NM_014975.2 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:21300357 C>T maps to NM_182515.3 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:21300357 C>T maps to NM_182515.3 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:22170087 C>T maps to NM_007153.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:22170087 C>T maps to NM_007153.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:45528912 C>T maps to ENST00000221452 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:45528912 C>T maps to ENST00000221452 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:51742807 T>A maps to NM_001772.3 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:51742807 T>A maps to NM_001772.3 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:54692108 G>C maps to NM_024298.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr19:54692108 G>C maps to NM_024298.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr2:56419778 G>A maps to NM_001080433.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr2:56419778 G>A maps to NM_001080433.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr2:135745304 G>A maps to NM_025052.3 N379N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr2:135745304 G>A maps to NM_025052.3 N379N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr2:141072661 G>T maps to NM_018557.2 S4216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr2:141072661 G>T maps to NM_018557.2 S4216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr2:187626380 C>T maps to NM_177454.3 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr2:187626380 C>T maps to NM_177454.3 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr2:198570719 C>G maps to NM_138395.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr2:198570719 C>G maps to NM_138395.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr2:220404982 G>A maps to NM_024536.5 R484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr2:220404982 G>A maps to NM_024536.5 R484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr2:241535794 C>T maps to NM_023083.3 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr2:241535794 C>T maps to NM_023083.3 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr20:377163 C>A maps to ENST00000422053 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr20:377163 C>A maps to ENST00000422053 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr20:2443870 C>T maps to ENST00000339610 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr20:2443870 C>T maps to ENST00000339610 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr20:33999834 C>T did not map to a codon.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr20:33999834 C>T did not map to a codon.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr21:47851583 G>T maps to NM_006031.5 E2736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr21:47851583 G>T maps to NM_006031.5 E2736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr3:33481235 G>A maps to NM_001128161.1 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr3:33481235 G>A maps to NM_001128161.1 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr3:38888754 C>A maps to ENST00000302328 V1602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr3:38888754 C>A maps to ENST00000302328 V1602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr3:152554041 C>T maps to NM_002563.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr3:152554041 C>T maps to NM_002563.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr3:167167166 G>A maps to NM_006217.3 Q330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr3:167167166 G>A maps to NM_006217.3 Q330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr3:183225975 G>A maps to NM_130446.2 N260N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr3:183225975 G>A maps to NM_130446.2 N260N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr4:57785988 C>G maps to NM_005612.4 S312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr4:57785988 C>G maps to NM_005612.4 S312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr5:7802383 G>A maps to NM_020546.2 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr5:7802383 G>A maps to NM_020546.2 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr5:113831872 T>C maps to NM_021614.2 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr5:113831872 T>C maps to NM_021614.2 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr6:22570124 G>A maps to NM_138574.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr6:22570124 G>A maps to NM_138574.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr6:33402926 A>T did not map to a codon.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr6:33402926 A>T did not map to a codon.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr8:8748456 G>A maps to NM_004225.2 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr8:8748456 G>A maps to NM_004225.2 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr9:140708935 C>T maps to NM_024757.4 L1078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chr9:140708935 C>T maps to NM_024757.4 L1078L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chrX:79281104 C>T maps to NM_016954.2 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4735-01A-01D-1434-08 chrX:79281104 C>T maps to NM_016954.2 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr1:60309253 C>T maps to NM_015888.4 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr1:60309253 C>T maps to NM_015888.4 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr1:149902779 C>T maps to NM_001145862.1 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr1:149902779 C>T maps to NM_001145862.1 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr1:161011573 C>T maps to NM_007122.3 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr1:161011573 C>T maps to NM_007122.3 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr11:5142406 C>A maps to NM_001005222.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr11:5142406 C>A maps to NM_001005222.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr11:56380078 G>A maps to NM_001004740.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr11:56380078 G>A maps to NM_001004740.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr11:58189993 G>T maps to NM_001005566.2 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr11:58189993 G>T maps to NM_001005566.2 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr12:14659875 G>A maps to NM_024829.5 R455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr12:14659875 G>A maps to NM_024829.5 R455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr12:125270877 G>A did not map to a codon.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr12:125270877 G>A did not map to a codon.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr13:20000606 A>G maps to NM_199254.2 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr13:20000606 A>G maps to NM_199254.2 G451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr17:10351236 C>T maps to NM_017533.2 K1621K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr17:10351236 C>T maps to NM_017533.2 K1621K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr17:12639604 C>T maps to NM_001146312.1 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr17:12639604 C>T maps to NM_001146312.1 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr18:3880017 G>A maps to NM_004746.2 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr18:3880017 G>A maps to NM_004746.2 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr19:16038132 C>A maps to NM_021187.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr19:16038132 C>A maps to NM_021187.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr2:164467455 G>A maps to NM_018086.2 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr2:164467455 G>A maps to NM_018086.2 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr20:18794839 G>A maps to NM_178483.2 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr20:18794839 G>A maps to NM_178483.2 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr3:36899180 G>A maps to NM_014831.2 Q634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr3:36899180 G>A maps to NM_014831.2 Q634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr4:25783862 C>T did not map to a codon.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr4:25783862 C>T did not map to a codon.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr5:115298652 G>A maps to NM_173800.4 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr5:115298652 G>A maps to NM_173800.4 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr5:150930201 C>T maps to NM_001447.2 V1509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr5:150930201 C>T maps to NM_001447.2 V1509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr7:76984547 C>A maps to NM_017439.3 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr7:76984547 C>A maps to NM_017439.3 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr7:91756927 C>T maps to NM_000786.3 K162K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr7:91756927 C>T maps to NM_000786.3 K162K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr7:129679337 C>T maps to NM_016478.3 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr7:129679337 C>T maps to NM_016478.3 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr8:89180108 T>A maps to NM_005941.4 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr8:89180108 T>A maps to NM_005941.4 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr9:21970999 C>A maps to NM_001195132.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chr9:21970999 C>A maps to NM_001195132.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chrX:155227435 C>A maps to NM_002186.2 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4736-01A-01D-1434-08 chrX:155227435 C>A maps to NM_002186.2 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr1:23191379 C>T maps to ENST00000400191 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr1:23191379 C>T maps to ENST00000400191 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr1:60139744 C>A maps to NM_001113411.1 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr1:60139744 C>A maps to NM_001113411.1 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr1:145311784 C>G did not map to a codon.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr1:145311784 C>G did not map to a codon.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr11:46637145 C>A maps to NM_173811.3 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr11:46637145 C>A maps to NM_173811.3 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr11:60561572 C>A maps to NM_206893.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr11:60561572 C>A maps to NM_206893.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr12:6666428 T>A maps to ENST00000382421 T756T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr12:6666428 T>A maps to ENST00000382421 T756T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr12:70956846 G>A maps to NM_001109754.1 S1315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr12:70956846 G>A maps to NM_001109754.1 S1315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr12:109610132 G>A maps to NM_001093.3 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr12:109610132 G>A maps to NM_001093.3 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr13:31205138 C>T maps to NM_005800.4 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr13:31205138 C>T maps to NM_005800.4 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr2:99949493 C>T maps to NM_005783.3 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr2:99949493 C>T maps to NM_005783.3 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr2:179399514 C>A maps to NM_133378.4 E31375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr2:179399514 C>A maps to NM_133378.4 E31375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr2:234652584 C>T did not map to a codon.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr2:234652584 C>T did not map to a codon.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr4:2641514 C>T maps to ENST00000324666 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr4:2641514 C>T maps to ENST00000324666 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr4:66270138 C>T maps to NM_004439.5 V581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr4:66270138 C>T maps to NM_004439.5 V581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr4:77675898 G>A maps to NM_020859.3 S1421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr4:77675898 G>A maps to NM_020859.3 S1421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr4:187518255 G>A maps to ENST00000260147 H4149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr4:187518255 G>A maps to ENST00000260147 H4149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr7:5104737 T>C maps to NM_021163.3 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr7:5104737 T>C maps to NM_021163.3 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr8:61765871 C>T maps to NM_017780.2 T2196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr8:61765871 C>T maps to NM_017780.2 T2196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr9:35107971 C>T maps to NM_025182.2 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr9:35107971 C>T maps to NM_025182.2 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr9:115759474 A>G maps to NM_001101338.1 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4737-01A-01D-1434-08 chr9:115759474 A>G maps to NM_001101338.1 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr1:10207076 G>A maps to NM_001105562.2 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr1:10207076 G>A maps to NM_001105562.2 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr1:23688995 G>A maps to NM_001077195.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr1:23688995 G>A maps to NM_001077195.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr1:44461304 C>T maps to NM_152499.1 C195C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr1:44461304 C>T maps to NM_152499.1 C195C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr1:152326394 T>C maps to NM_001014342.2 S1289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr1:152326394 T>C maps to NM_001014342.2 S1289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr1:217793360 C>T maps to NM_018040.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr1:217793360 C>T maps to NM_018040.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr1:227069673 G>A maps to ENST00000391872 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr1:227069673 G>A maps to ENST00000391872 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr10:106153148 A>G maps to NM_001008723.1 K530K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr10:106153148 A>G maps to NM_001008723.1 K530K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr11:5153038 G>A maps to NM_001005160.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr11:5153038 G>A maps to NM_001005160.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr11:8752203 C>T maps to NM_005418.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr11:8752203 C>T maps to NM_005418.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr11:12229645 C>T maps to NM_014632.2 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr11:12229645 C>T maps to NM_014632.2 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr11:46397932 G>A maps to NM_001105540.1 W904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr11:46397932 G>A maps to NM_001105540.1 W904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr11:66473194 G>A maps to NM_006946.2 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr11:66473194 G>A maps to NM_006946.2 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr11:102272785 G>C maps to NM_052932.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr11:102272785 G>C maps to NM_052932.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr12:111311765 G>A did not map to a codon.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr12:111311765 G>A did not map to a codon.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr15:88483889 G>T maps to NM_001012338.1 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr15:88483889 G>T maps to NM_001012338.1 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr16:21693073 G>T maps to ENST00000286149 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr16:21693073 G>T maps to ENST00000286149 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr17:27209177 G>A maps to ENST00000394906 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr17:27209177 G>A maps to ENST00000394906 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr17:37933963 G>A maps to NM_012481.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr17:37933963 G>A maps to NM_012481.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr17:74538649 G>A maps to NM_001077620.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr17:74538649 G>A maps to NM_001077620.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr2:25038609 G>A maps to NM_024322.2 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr2:25038609 G>A maps to NM_024322.2 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr2:32730181 G>T maps to NM_016252.3 E3204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr2:32730181 G>T maps to NM_016252.3 E3204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr2:73676155 T>A maps to NM_015120.4 A833A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr2:73676155 T>A maps to NM_015120.4 A833A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr2:201750419 C>T did not map to a codon.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr2:201750419 C>T did not map to a codon.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr20:333906 C>T maps to NM_024958.2 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr20:333906 C>T maps to NM_024958.2 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr20:23731350 G>A maps to NM_001898.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr20:23731350 G>A maps to NM_001898.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr20:60906172 G>A maps to NM_005560.3 L1189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr20:60906172 G>A maps to NM_005560.3 L1189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr22:19340888 G>A maps to NM_003325.3 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr22:19340888 G>A maps to NM_003325.3 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr3:49724468 G>A maps to NM_020998.3 Y213Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr3:49724468 G>A maps to NM_020998.3 Y213Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr3:50290577 C>T maps to NM_002070.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr3:50290577 C>T maps to NM_002070.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr3:118866241 C>T maps to NM_152539.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr3:118866241 C>T maps to NM_152539.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr4:104062021 G>C maps to NM_001813.2 L1901L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr4:104062021 G>C maps to NM_001813.2 L1901L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr6:93967233 T>A maps to NM_004440.3 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr6:93967233 T>A maps to NM_004440.3 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr6:99283870 C>G maps to NM_005604.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr6:99283870 C>G maps to NM_005604.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr6:102074477 G>A maps to NM_021956.4 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr6:102074477 G>A maps to NM_021956.4 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr6:123377031 C>T maps to NM_001010852.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr6:123377031 C>T maps to NM_001010852.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr7:11441596 T>A did not map to a codon.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr7:11441596 T>A did not map to a codon.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr7:19765250 G>A maps to NM_152774.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr7:19765250 G>A maps to NM_152774.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr7:77531082 T>C maps to ENST00000427986 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr7:77531082 T>C maps to ENST00000427986 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr8:124253496 G>C maps to NM_032847.1 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr8:124253496 G>C maps to NM_032847.1 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr9:100412849 C>T maps to NM_002486.4 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chr9:100412849 C>T maps to NM_002486.4 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chrX:15792451 A>T maps to NM_007220.3 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chrX:15792451 A>T maps to NM_007220.3 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chrX:91133548 G>T maps to NM_032968.3 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4738-01A-02D-1512-08 chrX:91133548 G>T maps to NM_032968.3 L770L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CN-4739-01A-02D-1512-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:40229410 G>T maps to NM_203456.2 T296T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CN-4739-01A-02D-1512-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:40229410 G>T maps to NM_203456.2 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:102270396 C>A maps to ENST00000338858 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:102270396 C>A maps to ENST00000338858 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:154459000 A>T did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:154459000 A>T did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:159850409 T>C maps to NM_012337.2 K326K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:159850409 T>C maps to NM_012337.2 K326K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:196971750 T>A maps to ENST00000367414 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:196971750 T>A maps to ENST00000367414 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:197396746 T>A maps to NM_201253.2 R764R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:197396746 T>A maps to NM_201253.2 R764R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:242277262 T>A maps to NM_152666.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:242277262 T>A maps to NM_152666.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:246704440 T>C maps to NM_022366.2 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr1:246704440 T>C maps to NM_022366.2 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr10:87482887 A>G maps to NM_017551.2 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr10:87482887 A>G maps to NM_017551.2 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr10:90122453 C>T maps to NM_001031709.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr10:90122453 C>T maps to NM_001031709.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr10:99343355 G>C maps to NM_020349.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr10:99343355 G>C maps to NM_020349.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr10:104860860 T>C did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr10:104860860 T>C did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr10:115895717 T>A maps to NM_018017.2 K482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr10:115895717 T>A maps to NM_018017.2 K482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr10:117226685 G>T maps to NM_207303.2 S1140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr10:117226685 G>T maps to NM_207303.2 S1140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr11:108160405 T>C maps to NM_000051.3 I1438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr11:108160405 T>C maps to NM_000051.3 I1438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr11:119243869 G>T maps to NM_004205.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr11:119243869 G>T maps to NM_004205.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr11:121016544 C>A maps to NM_005422.2 T1275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr11:121016544 C>A maps to NM_005422.2 T1275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr12:41961613 G>A maps to NM_001164595.1 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr12:41961613 G>A maps to NM_001164595.1 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr12:89918284 C>T maps to NM_003774.4 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr12:89918284 C>T maps to NM_003774.4 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr12:113515367 C>T maps to NM_004416.2 Y133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr12:113515367 C>T maps to NM_004416.2 Y133Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr14:105932763 G>A maps to NM_004689.3 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr14:105932763 G>A maps to NM_004689.3 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr15:99467896 C>T maps to NM_000875.3 F922F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr15:99467896 C>T maps to NM_000875.3 F922F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr16:19612992 C>G maps to NM_020314.5 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr16:19612992 C>G maps to NM_020314.5 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr16:24580863 A>T maps to NM_006910.4 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr16:24580863 A>T maps to NM_006910.4 P951P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr16:50763773 G>T maps to NM_022162.1 L1004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr16:50763773 G>T maps to NM_022162.1 L1004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr16:53708988 C>T maps to NM_015272.2 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr16:53708988 C>T maps to NM_015272.2 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr16:85822626 G>A maps to NM_006067.4 Y87Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr16:85822626 G>A maps to NM_006067.4 Y87Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr17:27185505 T>C did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr17:27185505 T>C did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr17:67218722 A>G maps to NM_080282.3 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr17:67218722 A>G maps to NM_080282.3 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr18:12325642 C>A maps to NM_032525.1 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr18:12325642 C>A maps to NM_032525.1 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr18:32345947 C>T maps to NM_001390.4 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr18:32345947 C>T maps to NM_001390.4 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr19:1042122 G>T maps to NM_019112.3 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr19:1042122 G>T maps to NM_019112.3 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr19:2717399 C>G maps to NM_145173.3 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr19:2717399 C>G maps to NM_145173.3 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr19:3009611 C>A maps to NM_003260.4 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr19:3009611 C>A maps to NM_003260.4 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr19:4292862 G>A maps to NM_144615.2 N194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr19:4292862 G>A maps to NM_144615.2 N194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr19:48908442 A>C maps to NM_000836.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr19:48908442 A>C maps to NM_000836.2 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr19:56466302 T>A maps to NM_176811.2 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr19:56466302 T>A maps to NM_176811.2 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr19:56552286 G>T did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr19:56552286 G>T did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr2:39934300 G>A maps to NM_152390.2 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr2:39934300 G>A maps to NM_152390.2 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr2:85581596 G>A maps to NM_017750.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr2:85581596 G>A maps to NM_017750.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr2:141643800 T>A maps to NM_018557.2 T1290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr2:141643800 T>A maps to NM_018557.2 T1290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr2:158283871 C>T maps to NM_004288.4 Q179Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr2:158283871 C>T maps to NM_004288.4 Q179Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr2:220369976 G>A maps to ENST00000373917 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr2:220369976 G>A maps to ENST00000373917 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr2:223158888 G>T maps to NM_181459.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr2:223158888 G>T maps to NM_181459.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr20:485835 G>A maps to NM_177559.2 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr20:485835 G>A maps to NM_177559.2 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr20:3209784 G>A maps to NM_001174090.1 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr20:3209784 G>A maps to NM_001174090.1 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr20:54824141 G>A maps to ENST00000371389 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr20:54824141 G>A maps to ENST00000371389 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr21:39755447 G>A maps to NM_001136154.1 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr21:39755447 G>A maps to NM_001136154.1 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr22:21989392 G>A maps to NM_152612.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr22:21989392 G>A maps to NM_152612.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr22:37769204 G>A maps to NM_052906.3 H790H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr22:37769204 G>A maps to NM_052906.3 H790H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr3:65350390 G>A maps to NM_001033057.1 T1100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr3:65350390 G>A maps to NM_001033057.1 T1100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr3:72495695 C>A maps to ENST00000477973 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr3:72495695 C>A maps to ENST00000477973 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr3:160095272 G>A maps to ENST00000326448 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr3:160095272 G>A maps to ENST00000326448 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr4:41983734 C>T did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr4:41983734 C>T did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr4:109681434 C>T maps to NM_031279.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr4:109681434 C>T maps to NM_031279.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr4:118974942 A>G did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr4:118974942 A>G did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr5:24488014 C>A maps to NM_006727.3 T708T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr5:24488014 C>A maps to NM_006727.3 T708T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr5:39341763 A>G maps to NM_001737.3 N74N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr5:39341763 A>G maps to NM_001737.3 N74N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr5:101795456 T>C maps to NM_173488.3 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr5:101795456 T>C maps to NM_173488.3 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr5:145979964 C>A maps to ENST00000394414 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr5:145979964 C>A maps to ENST00000394414 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr7:2559806 C>T maps to NM_001040167.1 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr7:2559806 C>T maps to NM_001040167.1 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr7:34724267 C>T maps to NM_207172.1 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr7:34724267 C>T maps to NM_207172.1 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr7:37780084 C>T maps to NM_181791.1 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr7:37780084 C>T maps to NM_181791.1 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr8:3059158 G>A maps to NM_033225.5 L1691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr8:3059158 G>A maps to NM_033225.5 L1691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr8:41530293 G>A maps to ENST00000415018 D1558D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr8:41530293 G>A maps to ENST00000415018 D1558D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr8:55540809 A>G maps to NM_006269.1 T1456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr8:55540809 A>G maps to NM_006269.1 T1456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr8:63492236 T>C did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr8:63492236 T>C did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr9:2718221 C>G maps to NM_133497.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr9:2718221 C>G maps to NM_133497.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr9:125797358 G>T maps to NM_005294.1 G172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr9:125797358 G>T maps to NM_005294.1 G172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr9:127089615 G>A did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr9:127089615 G>A did not map to a codon.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr9:138377301 G>T maps to NM_014811.3 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chr9:138377301 G>T maps to NM_014811.3 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chrX:130416469 C>T maps to NM_001170961.1 W398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chrX:130416469 C>T maps to NM_001170961.1 W398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chrX:139866495 G>A maps to NM_004065.2 D12D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4739-01A-02D-1512-08 chrX:139866495 G>A maps to NM_004065.2 D12D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:985676 G>C maps to NM_198576.2 L1648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:985676 G>C maps to NM_198576.2 L1648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:1277123 G>A maps to ENST00000378888 D176D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:1277123 G>A maps to ENST00000378888 D176D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:21560051 G>A maps to NM_001397.2 Q557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:21560051 G>A maps to NM_001397.2 Q557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:33292422 C>A maps to NM_022753.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:33292422 C>A maps to NM_022753.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:111738608 G>A maps to NM_024901.3 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:111738608 G>A maps to NM_024901.3 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:183532570 C>T maps to NM_001127651.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:183532570 C>T maps to NM_001127651.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:203311479 G>A maps to NM_002023.3 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:203311479 G>A maps to NM_002023.3 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr10:6139142 C>T maps to NM_001145547.1 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr10:6139142 C>T maps to NM_001145547.1 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr10:88988215 C>T maps to NM_001099338.1 C193C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr10:88988215 C>T maps to NM_001099338.1 C193C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr11:2434716 G>A maps to ENST00000452833 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr11:2434716 G>A maps to ENST00000452833 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr12:39696847 G>A maps to ENST00000395670 T1551T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr12:39696847 G>A maps to ENST00000395670 T1551T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr12:56975651 T>C maps to NM_002898.3 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr12:56975651 T>C maps to NM_002898.3 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr12:57858618 C>T maps to NM_005269.2 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr12:57858618 C>T maps to NM_005269.2 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr14:34145430 C>G maps to NM_001164749.1 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr14:34145430 C>G maps to NM_001164749.1 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr14:55457984 C>T maps to NM_007086.3 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr14:55457984 C>T maps to NM_007086.3 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr15:42116701 C>T maps to NM_001128608.1 Q1418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr15:42116701 C>T maps to NM_001128608.1 Q1418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr15:42457993 C>T maps to ENST00000348544 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr15:42457993 C>T maps to ENST00000348544 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr16:3820843 G>C maps to NM_004380.2 L869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr16:3820843 G>C maps to NM_004380.2 L869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr16:57829030 G>C maps to NM_005550.3 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr16:57829030 G>C maps to NM_005550.3 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr16:70841773 C>T maps to NM_032821.2 K5024K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr16:70841773 C>T maps to NM_032821.2 K5024K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr16:84093016 C>T maps to NM_003791.2 R907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr16:84093016 C>T maps to NM_003791.2 R907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr17:7578523 G>A maps to NM_001126112.1 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr17:7578523 G>A maps to NM_001126112.1 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr17:67149443 A>T did not map to a codon.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr17:67149443 A>T did not map to a codon.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr17:79058641 C>T maps to NM_017451.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr17:79058641 C>T maps to NM_017451.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr18:55218579 A>G maps to NM_001012515.2 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr18:55218579 A>G maps to NM_001012515.2 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr18:56203583 G>A maps to NM_052947.3 L1279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr18:56203583 G>A maps to NM_052947.3 L1279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr19:7809919 G>A maps to NM_021155.3 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr19:7809919 G>A maps to NM_021155.3 F269F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr19:10664770 C>T maps to NM_023008.3 R662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr19:10664770 C>T maps to NM_023008.3 R662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr19:36562558 C>T maps to NM_001083961.1 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr19:36562558 C>T maps to NM_001083961.1 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr2:128865572 C>G maps to NM_020120.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr2:128865572 C>G maps to NM_020120.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr2:179497063 C>T maps to NM_133378.4 E11951E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr2:179497063 C>T maps to NM_133378.4 E11951E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr2:219736444 C>T maps to NM_006522.3 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr2:219736444 C>T maps to NM_006522.3 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr20:31572919 C>T maps to NM_080675.3 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr20:31572919 C>T maps to NM_080675.3 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr22:20049074 G>A maps to NM_152906.4 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr22:20049074 G>A maps to NM_152906.4 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr22:30953271 C>T maps to NM_004861.1 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr22:30953271 C>T maps to NM_004861.1 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr4:5862864 G>A maps to NM_001014809.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr4:5862864 G>A maps to NM_001014809.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr4:41748273 G>A maps to NM_003924.3 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr4:41748273 G>A maps to NM_003924.3 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr4:57190421 G>A maps to NM_020722.1 T1177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr4:57190421 G>A maps to NM_020722.1 T1177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr4:68725341 G>A maps to NM_004262.2 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr4:68725341 G>A maps to NM_004262.2 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr4:71507742 T>C maps to NM_031889.2 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr4:71507742 T>C maps to NM_031889.2 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr4:166254490 G>T did not map to a codon.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr4:166254490 G>T did not map to a codon.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr5:140530096 G>T maps to NM_018939.2 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr5:140530096 G>T maps to NM_018939.2 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr5:167674087 C>T maps to NM_001122679.1 V2039V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr5:167674087 C>T maps to NM_001122679.1 V2039V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr6:28333969 C>T maps to NM_024493.2 Q509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr6:28333969 C>T maps to NM_024493.2 Q509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr6:31918537 C>T maps to ENST00000437789 G1091G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr6:31918537 C>T maps to ENST00000437789 G1091G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr6:88127959 C>T maps to NM_001031743.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr6:88127959 C>T maps to NM_001031743.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr7:99707582 C>T maps to ENST00000472509 Q481Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr7:99707582 C>T maps to ENST00000472509 Q481Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr7:99711568 C>T maps to ENST00000472509 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr7:99711568 C>T maps to ENST00000472509 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr7:99711748 G>A maps to ENST00000472509 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr7:99711748 G>A maps to ENST00000472509 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr7:150325562 C>A maps to ENST00000438845 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr7:150325562 C>A maps to ENST00000438845 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chrX:38156555 G>T maps to NM_001034853.1 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chrX:38156555 G>T maps to NM_001034853.1 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chrX:104464802 C>A maps to NM_031274.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chrX:104464802 C>A maps to NM_031274.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr1:46471916 C>G maps to NM_015112.2 S251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr1:46471916 C>G maps to NM_015112.2 S251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr1:62954603 C>A did not map to a codon.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr1:62954603 C>A did not map to a codon.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr1:74492541 C>T maps to NM_001105659.1 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr1:74492541 C>T maps to NM_001105659.1 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr1:102312597 G>A did not map to a codon.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr1:102312597 G>A did not map to a codon.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr1:109794494 G>C maps to NM_001408.2 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr1:109794494 G>C maps to NM_001408.2 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr1:198701642 C>T maps to ENST00000271610 N700N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr1:198701642 C>T maps to ENST00000271610 N700N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr1:231064750 G>A maps to NM_024525.4 H463H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr1:231064750 G>A maps to NM_024525.4 H463H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr10:74645513 C>T maps to NM_138357.1 D330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr10:74645513 C>T maps to NM_138357.1 D330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr10:105330707 C>T maps to NM_004210.4 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr10:105330707 C>T maps to NM_004210.4 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr11:118376146 C>T maps to NM_001197104.1 I3180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr11:118376146 C>T maps to NM_001197104.1 I3180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr12:6833911 C>T maps to NM_001164093.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr12:6833911 C>T maps to NM_001164093.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr12:13224218 C>T maps to NM_020853.1 Y471Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr12:13224218 C>T maps to NM_020853.1 Y471Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr12:49443898 C>A maps to NM_003482.3 E1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr12:49443898 C>A maps to NM_003482.3 E1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr12:49719905 C>T maps to NM_005480.3 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr12:49719905 C>T maps to NM_005480.3 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr12:121206201 C>T maps to NM_139015.3 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr12:121206201 C>T maps to NM_139015.3 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr13:36241641 C>T maps to ENST00000400445 R2845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr13:36241641 C>T maps to ENST00000400445 R2845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr15:40241350 C>G maps to NM_001013703.2 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr15:40241350 C>G maps to NM_001013703.2 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr15:91454653 C>T maps to NM_006122.2 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr15:91454653 C>T maps to NM_006122.2 F661F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr16:2288403 C>T maps to NM_001374.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr16:2288403 C>T maps to NM_001374.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr16:22344978 C>T maps to NM_018119.2 S695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr16:22344978 C>T maps to NM_018119.2 S695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr16:75512967 G>A maps to NM_021615.4 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr16:75512967 G>A maps to NM_021615.4 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr16:78064471 G>T maps to NM_005752.3 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr16:78064471 G>T maps to NM_005752.3 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr17:33343398 G>C maps to NM_001017368.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr17:33343398 G>C maps to NM_001017368.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr17:34068185 C>T maps to NM_033315.3 C158C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr17:34068185 C>T maps to NM_033315.3 C158C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr17:57165710 T>C maps to NM_015294.3 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr17:57165710 T>C maps to NM_015294.3 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr17:71166309 C>T maps to NM_001050.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr17:71166309 C>T maps to NM_001050.2 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:2213554 C>T maps to ENST00000221482 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:2213554 C>T maps to ENST00000221482 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:17845128 C>T maps to NM_018174.4 Y1024Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:17845128 C>T maps to NM_018174.4 Y1024Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:37903738 T>C maps to NM_152484.2 E607E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:37903738 T>C maps to NM_152484.2 E607E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:39297124 G>A maps to NM_006149.3 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:39297124 G>A maps to NM_006149.3 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:46206183 C>T maps to NM_017659.3 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:46206183 C>T maps to NM_017659.3 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:54803658 C>T maps to ENST00000251375 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:54803658 C>T maps to ENST00000251375 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:55494890 C>T maps to NM_017852.3 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:55494890 C>T maps to NM_017852.3 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr2:61597494 C>T maps to NM_014709.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr2:61597494 C>T maps to NM_014709.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr2:220116385 G>A maps to NM_006000.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr2:220116385 G>A maps to NM_006000.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr2:220338271 C>T maps to NM_005876.4 I1398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr2:220338271 C>T maps to NM_005876.4 I1398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr2:220501430 C>G maps to NM_201574.2 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr2:220501430 C>G maps to NM_201574.2 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr20:62839235 C>T maps to NM_004535.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr20:62839235 C>T maps to NM_004535.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr21:46074246 G>A maps to NM_198698.1 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr21:46074246 G>A maps to NM_198698.1 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr22:21138320 G>A maps to NM_000185.3 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr22:21138320 G>A maps to NM_000185.3 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr22:43275153 G>A maps to NM_001184970.1 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr22:43275153 G>A maps to NM_001184970.1 R310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:45744941 T>C maps to NM_014016.3 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:45744941 T>C maps to NM_014016.3 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:46399947 G>A maps to NM_001123041.2 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:46399947 G>A maps to NM_001123041.2 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:52404530 C>T maps to ENST00000273600 I2099I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:52404530 C>T maps to ENST00000273600 I2099I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:52867432 C>T maps to ENST00000504329 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:52867432 C>T maps to ENST00000504329 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:97887884 C>G maps to NM_001005515.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:97887884 C>G maps to NM_001005515.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:111769614 T>C maps to ENST00000443106 C384C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:111769614 T>C maps to ENST00000443106 C384C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:184008347 G>A maps to NM_014693.3 W671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:184008347 G>A maps to NM_014693.3 W671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:195486031 G>A maps to NM_018406.5 F4983F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:195486031 G>A maps to NM_018406.5 F4983F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:195517518 G>C maps to NM_018406.5 S311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr3:195517518 G>C maps to NM_018406.5 S311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr4:40936490 G>A maps to NM_004307.1 N412N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr4:40936490 G>A maps to NM_004307.1 N412N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr4:96762281 C>T maps to NM_005390.4 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr4:96762281 C>T maps to NM_005390.4 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr4:157771473 C>G maps to NM_016205.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr4:157771473 C>G maps to NM_016205.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr5:41199908 C>A maps to NM_001115131.1 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr5:41199908 C>A maps to NM_001115131.1 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr5:113699623 C>T maps to NM_021614.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr5:113699623 C>T maps to NM_021614.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr5:179201800 C>T maps to NM_014757.4 L992L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr5:179201800 C>T maps to NM_014757.4 L992L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr6:41162431 G>C maps to ENST00000373108 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr6:41162431 G>C maps to ENST00000373108 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr6:82923969 T>C maps to NM_015525.2 K726K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr6:82923969 T>C maps to NM_015525.2 K726K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr8:86389458 G>A maps to NM_000067.2 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr8:86389458 G>A maps to NM_000067.2 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr9:115760137 G>A maps to NM_001101338.1 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr9:115760137 G>A maps to NM_001101338.1 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chrX:1409268 C>T maps to NM_001161530.1 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chrX:1409268 C>T maps to NM_001161530.1 D171D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chrX:21875243 G>A maps to NM_206923.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chrX:21875243 G>A maps to NM_206923.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chrX:70823702 C>T maps to NM_052957.4 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chrX:70823702 C>T maps to NM_052957.4 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr1:27690422 G>A maps to NM_004672.3 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr1:27690422 G>A maps to NM_004672.3 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr1:102290780 G>A maps to ENST00000338858 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr1:102290780 G>A maps to ENST00000338858 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr1:152192430 A>G maps to NM_001009931.1 Y558Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr1:152192430 A>G maps to NM_001009931.1 Y558Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr11:40137211 C>A maps to NM_020929.1 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr11:40137211 C>A maps to NM_020929.1 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr11:111731327 C>T maps to ENST00000428306 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr11:111731327 C>T maps to ENST00000428306 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr12:56380869 A>G maps to NM_002868.2 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr12:56380869 A>G maps to NM_002868.2 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr12:78598822 C>T maps to NM_014903.4 R2293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr12:78598822 C>T maps to NM_014903.4 R2293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr12:130184665 C>T maps to NM_133448.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr12:130184665 C>T maps to NM_133448.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr16:15122789 G>A maps to NM_015027.2 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr16:15122789 G>A maps to NM_015027.2 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr16:47117172 G>A maps to NM_018092.3 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr16:47117172 G>A maps to NM_018092.3 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr17:5357157 G>A maps to ENST00000457531 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr17:5357157 G>A maps to ENST00000457531 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr17:7577057 C>A maps to NM_001126112.1 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr17:7577057 C>A maps to NM_001126112.1 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr17:30815309 C>T maps to NM_003885.2 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr17:30815309 C>T maps to NM_003885.2 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr17:59946708 G>A maps to NM_020748.2 V1029V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr17:59946708 G>A maps to NM_020748.2 V1029V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr19:9064690 T>A maps to NM_024690.2 T7585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr19:9064690 T>A maps to NM_024690.2 T7585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr19:10602731 C>T maps to NM_203500.1 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr19:10602731 C>T maps to NM_203500.1 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr19:37880351 A>G maps to NM_032453.1 E467E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr19:37880351 A>G maps to NM_032453.1 E467E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr2:176958145 C>T maps to NM_000523.3 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr2:176958145 C>T maps to NM_000523.3 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr2:238253406 G>A maps to NM_004369.3 F2418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr2:238253406 G>A maps to NM_004369.3 F2418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr20:3052919 C>T maps to NM_000915.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr20:3052919 C>T maps to NM_000915.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr22:29730293 G>A maps to NM_001127.3 Q757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr22:29730293 G>A maps to NM_001127.3 Q757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr3:9547693 C>T maps to NM_198560.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr3:9547693 C>T maps to NM_198560.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr3:51979164 G>A maps to NM_001003931.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr3:51979164 G>A maps to NM_001003931.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr3:122354764 C>T maps to NM_001113523.1 R619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr3:122354764 C>T maps to NM_001113523.1 R619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr4:178272609 A>T maps to NM_018248.2 K316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr4:178272609 A>T maps to NM_018248.2 K316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr5:145641353 C>T maps to NM_018989.1 H725H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr5:145641353 C>T maps to NM_018989.1 H725H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr7:4856926 C>T maps to NM_018059.4 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr7:4856926 C>T maps to NM_018059.4 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr7:11630168 C>T maps to ENST00000423059 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr7:11630168 C>T maps to ENST00000423059 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr7:86826066 C>T maps to NM_024315.2 W81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr7:86826066 C>T maps to NM_024315.2 W81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chrX:99917201 C>T maps to NM_014467.2 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chrX:99917201 C>T maps to NM_014467.2 Q65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chrX:134305096 G>A did not map to a codon.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chrX:134305096 G>A did not map to a codon.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chrX:153130402 G>A maps to NM_000425.3 P973P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chrX:153130402 G>A maps to NM_000425.3 P973P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr1:196205129 C>T maps to NM_198503.2 E1094E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr1:196205129 C>T maps to NM_198503.2 E1094E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr10:45480279 G>A maps to NM_032023.3 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr10:45480279 G>A maps to NM_032023.3 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr10:46121635 C>T maps to NM_001128324.1 E545E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr10:46121635 C>T maps to NM_001128324.1 E545E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr10:60546841 G>C did not map to a codon.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr10:60546841 G>C did not map to a codon.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr11:57176683 G>A maps to ENST00000428603 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr11:57176683 G>A maps to ENST00000428603 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr12:9256906 G>A maps to NM_000014.4 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr12:9256906 G>A maps to NM_000014.4 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr12:73014919 T>C maps to NM_013381.2 Y789Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr12:73014919 T>C maps to NM_013381.2 Y789Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr15:52672047 G>A maps to ENST00000358212 I690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr15:52672047 G>A maps to ENST00000358212 I690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr15:54919299 G>T maps to ENST00000260323 E2212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr15:54919299 G>T maps to ENST00000260323 E2212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr15:91557071 G>A maps to NM_018668.3 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr15:91557071 G>A maps to NM_018668.3 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr16:86601396 C>A maps to NM_005251.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr16:86601396 C>A maps to NM_005251.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr17:7576852 C>T maps to NM_001126112.1 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr17:7576852 C>T maps to NM_001126112.1 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr17:7755571 G>A maps to NM_001080424.1 V1462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr17:7755571 G>A maps to NM_001080424.1 V1462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr17:7801354 G>T maps to NM_001005271.2 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr17:7801354 G>T maps to NM_001005271.2 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr19:53116710 A>G maps to NM_018300.3 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr19:53116710 A>G maps to NM_018300.3 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr19:54780727 C>G maps to ENST00000391747 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr19:54780727 C>G maps to ENST00000391747 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr2:101087009 A>G maps to NM_001011717.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr2:101087009 A>G maps to NM_001011717.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr2:228173693 A>T maps to NM_000091.4 A1514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr2:228173693 A>T maps to NM_000091.4 A1514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr22:17072996 G>A maps to NM_014406.4 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr22:17072996 G>A maps to NM_014406.4 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr3:53699744 C>A maps to NM_001128840.1 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr3:53699744 C>A maps to NM_001128840.1 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr3:146171941 G>A maps to ENST00000497985 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr3:146171941 G>A maps to ENST00000497985 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr3:172835422 G>C maps to NM_031955.5 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr3:172835422 G>C maps to NM_031955.5 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr3:194062540 G>A maps to NM_001080513.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr3:194062540 G>A maps to NM_001080513.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr4:134071804 C>T maps to NM_032961.1 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr4:134071804 C>T maps to NM_032961.1 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr4:144826670 C>T did not map to a codon.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr4:144826670 C>T did not map to a codon.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr5:54275231 A>G maps to NM_007036.4 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr5:54275231 A>G maps to NM_007036.4 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr5:159821392 C>A maps to NM_022090.3 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr5:159821392 C>A maps to NM_022090.3 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr5:159992485 G>T maps to NM_025153.2 R1454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr5:159992485 G>T maps to NM_025153.2 R1454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr6:80720549 A>G maps to NM_003318.4 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr6:80720549 A>G maps to NM_003318.4 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr7:6731083 C>A maps to ENST00000330442 E554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr7:6731083 C>A maps to ENST00000330442 E554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr8:69028101 T>C maps to NM_024870.2 F1087F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr8:69028101 T>C maps to NM_024870.2 F1087F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr9:6330997 G>A maps to NM_001001874.2 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr9:6330997 G>A maps to NM_001001874.2 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr9:111617802 G>A maps to NM_006686.3 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr9:111617802 G>A maps to NM_006686.3 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr9:139401755 C>T did not map to a codon.
Sequencing variant TCGA-CN-5355-01A-01D-1434-08 chr9:139401755 C>T did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:1572345 C>T maps to ENST00000401097 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:1572345 C>T maps to ENST00000401097 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:36552863 G>T maps to NM_014466.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:36552863 G>T maps to NM_014466.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:104115821 T>C maps to ENST00000305865 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:104115821 T>C maps to ENST00000305865 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:158585169 C>T maps to NM_003126.2 A2208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:158585169 C>T maps to NM_003126.2 A2208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:158669836 G>C maps to NM_001005279.1 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:158669836 G>C maps to NM_001005279.1 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:159897612 G>A maps to NM_001135050.1 L1099L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:159897612 G>A maps to NM_001135050.1 L1099L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:183105650 T>G maps to NM_002293.3 A1415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:183105650 T>G maps to NM_002293.3 A1415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:197128770 C>T maps to NM_194314.2 Q816Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:197128770 C>T maps to NM_194314.2 Q816Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:201839979 C>T maps to NM_018085.4 V801V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:201839979 C>T maps to NM_018085.4 V801V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:216074209 G>A maps to ENST00000366943 A2446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:216074209 G>A maps to ENST00000366943 A2446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:237935318 G>A maps to NM_001035.2 Q3855Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr1:237935318 G>A maps to NM_001035.2 Q3855Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr10:32128564 T>C maps to NM_018287.5 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr10:32128564 T>C maps to NM_018287.5 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr10:56106238 A>T maps to NM_001142763.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr10:56106238 A>T maps to NM_001142763.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr10:56138616 C>A maps to NM_001142763.1 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr10:56138616 C>A maps to NM_001142763.1 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr10:82187165 C>T maps to NM_032333.4 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr10:82187165 C>T maps to NM_032333.4 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:2189384 G>T maps to NM_199292.2 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:2189384 G>T maps to NM_199292.2 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:4608359 G>C maps to NM_001005170.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:4608359 G>C maps to NM_001005170.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:6867338 G>T maps to ENST00000379831 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:6867338 G>T maps to ENST00000379831 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:6867356 T>C maps to ENST00000379831 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:6867356 T>C maps to ENST00000379831 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:6891365 T>A maps to NM_001004460.1 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:6891365 T>A maps to NM_001004460.1 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:20939792 A>G maps to NM_006157.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:20939792 A>G maps to NM_006157.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:21581765 C>T maps to NM_006157.3 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:21581765 C>T maps to NM_006157.3 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:44297070 A>G maps to NM_021926.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:44297070 A>G maps to NM_021926.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:78279725 C>A maps to NM_024678.4 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:78279725 C>A maps to NM_024678.4 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:95564302 G>A maps to NM_014679.3 K462K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:95564302 G>A maps to NM_014679.3 K462K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:102663348 G>A maps to NM_002421.3 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:102663348 G>A maps to NM_002421.3 V340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:124761402 A>G maps to NM_019055.5 T580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr11:124761402 A>G maps to NM_019055.5 T580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr12:48141545 G>T maps to NM_001098531.2 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr12:48141545 G>T maps to NM_001098531.2 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr12:51834518 C>T maps to NM_001039960.1 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr12:51834518 C>T maps to NM_001039960.1 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr12:73056936 G>T maps to NM_013381.2 E1013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr12:73056936 G>T maps to NM_013381.2 E1013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr12:113730844 G>T maps to NM_001143819.1 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr12:113730844 G>T maps to NM_001143819.1 L812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr12:120876215 G>T maps to NM_004373.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr12:120876215 G>T maps to NM_004373.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr12:133266847 G>A did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr12:133266847 G>A did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr13:25265202 G>T maps to NM_001185085.1 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr13:25265202 G>T maps to NM_001185085.1 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr14:20528871 C>A maps to NM_001004717.1 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr14:20528871 C>A maps to NM_001004717.1 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr14:23846489 G>A maps to ENST00000339180 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr14:23846489 G>A maps to ENST00000339180 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr14:37777651 G>A maps to NM_001195296.1 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr14:37777651 G>A maps to NM_001195296.1 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr14:77327046 G>T maps to NM_194287.2 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr14:77327046 G>T maps to NM_194287.2 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr15:43927950 G>A maps to NM_172095.1 D365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr15:43927950 G>A maps to NM_172095.1 D365D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr15:44941066 T>A maps to NM_025137.3 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr15:44941066 T>A maps to NM_025137.3 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr16:1374784 G>T maps to NM_194259.1 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr16:1374784 G>T maps to NM_194259.1 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr16:3487032 G>A maps to NM_152457.1 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr16:3487032 G>A maps to NM_152457.1 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:2238907 C>T maps to NM_018128.4 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:2238907 C>T maps to NM_018128.4 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:3844429 C>T maps to NM_174953.1 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:3844429 C>T maps to NM_174953.1 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:27085473 G>T maps to NM_018182.2 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:27085473 G>T maps to NM_018182.2 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:36483634 T>A maps to ENST00000398597 T1940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:36483634 T>A maps to ENST00000398597 T1940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:37879628 G>T maps to NM_004448.2 G668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:37879628 G>T maps to NM_004448.2 G668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:39502481 G>A maps to NM_004138.2 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:39502481 G>A maps to NM_004138.2 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:41141509 G>C maps to NM_173079.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:41141509 G>C maps to NM_173079.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:45481246 T>A maps to NM_152347.4 L674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:45481246 T>A maps to NM_152347.4 L674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:48601146 T>A did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:48601146 T>A did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:53471829 G>A maps to NM_012329.2 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr17:53471829 G>A maps to NM_012329.2 F194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr18:25585918 C>T maps to NM_001792.3 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr18:25585918 C>T maps to NM_001792.3 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr18:50278743 G>T maps to NM_005215.3 G138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr18:50278743 G>T maps to NM_005215.3 G138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr18:77246596 C>T maps to NM_172387.1 P801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr18:77246596 C>T maps to NM_172387.1 P801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:2109207 T>C did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:2109207 T>C did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:2226521 T>C maps to ENST00000221482 G1334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:2226521 T>C maps to ENST00000221482 G1334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:4504668 C>T maps to NM_001080400.1 R1292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:4504668 C>T maps to NM_001080400.1 R1292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:8138158 C>A maps to NM_032447.3 S2575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:8138158 C>A maps to NM_032447.3 S2575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:22939864 T>C maps to ENST00000397104 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:22939864 T>C maps to ENST00000397104 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:42730363 A>G maps to NM_133444.1 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:42730363 A>G maps to NM_133444.1 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:54849457 G>C maps to NM_012276.3 S135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:54849457 G>C maps to NM_012276.3 S135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:58565247 C>A maps to NM_182572.3 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:58565247 C>A maps to NM_182572.3 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:58864485 G>A maps to NM_130786.3 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr19:58864485 G>A maps to NM_130786.3 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr2:5832930 C>T maps to NM_003108.3 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr2:5832930 C>T maps to NM_003108.3 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr2:45233599 A>G maps to NM_016932.4 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr2:45233599 A>G maps to NM_016932.4 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr2:127957113 G>A maps to NM_001001665.3 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr2:127957113 G>A maps to NM_001001665.3 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr2:160084426 T>A maps to NM_033394.2 L1334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr2:160084426 T>A maps to NM_033394.2 L1334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr2:225651807 T>C maps to NM_014689.2 K1862K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr2:225651807 T>C maps to NM_014689.2 K1862K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr20:36954719 C>A maps to NM_001725.2 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr20:36954719 C>A maps to NM_001725.2 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr22:37708146 C>A maps to NM_013385.3 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr22:37708146 C>A maps to NM_013385.3 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr22:39421331 T>C maps to NM_152426.3 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr22:39421331 T>C maps to NM_152426.3 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr22:39883966 G>A maps to NM_001098270.1 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr22:39883966 G>A maps to NM_001098270.1 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:2778010 A>T maps to NM_175607.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:2778010 A>T maps to NM_175607.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:40275390 C>A maps to NM_015460.2 V649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:40275390 C>A maps to NM_015460.2 V649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:52558126 T>C maps to NM_015136.2 D2518D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:52558126 T>C maps to NM_015136.2 D2518D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:73433787 G>A maps to NM_015009.1 C643C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:73433787 G>A maps to NM_015009.1 C643C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:98217105 C>T maps to NM_001004737.1 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:98217105 C>T maps to NM_001004737.1 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:148558762 G>T did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:148558762 G>T did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:154013096 C>T maps to NM_020865.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:154013096 C>T maps to NM_020865.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:154055727 T>A maps to NM_001038705.1 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr3:154055727 T>A maps to NM_001038705.1 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr4:114278086 C>T maps to NM_001148.4 I2771I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr4:114278086 C>T maps to NM_001148.4 I2771I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr4:123542010 A>G maps to NM_021803.2 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr4:123542010 A>G maps to NM_021803.2 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr4:139981704 A>G maps to ENST00000379550 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr4:139981704 A>G maps to ENST00000379550 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr4:149357709 T>C maps to ENST00000511528 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr4:149357709 T>C maps to ENST00000511528 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr4:155156537 G>C maps to NM_017639.3 S2634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr4:155156537 G>C maps to NM_017639.3 S2634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr4:158065103 G>T maps to NM_001166060.1 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr4:158065103 G>T maps to NM_001166060.1 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr4:165118777 G>T maps to NM_012403.1 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr4:165118777 G>T maps to NM_012403.1 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:5235235 G>T maps to NM_139056.2 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:5235235 G>T maps to NM_139056.2 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:23527818 C>T maps to NM_020227.2 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:23527818 C>T maps to NM_020227.2 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:26890581 C>A maps to NM_016279.3 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:26890581 C>A maps to NM_016279.3 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:68473451 G>A maps to NM_031966.2 K432K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:68473451 G>A maps to NM_031966.2 K432K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:76607879 T>A did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:76607879 T>A did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:79029871 A>T maps to NM_153610.3 K1762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:79029871 A>T maps to NM_153610.3 K1762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:80363997 G>A maps to NM_006909.1 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:80363997 G>A maps to NM_006909.1 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:130815437 C>A maps to ENST00000514667 E667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:130815437 C>A maps to ENST00000514667 E667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:137496707 G>A maps to NM_139199.1 R767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:137496707 G>A maps to NM_139199.1 R767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:140250499 G>T maps to NM_018902.3 A604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:140250499 G>T maps to NM_018902.3 A604A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:140516464 C>T maps to NM_015669.2 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:140516464 C>T maps to NM_015669.2 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:141974898 G>A maps to NM_001144935.1 Q142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:141974898 G>A maps to NM_001144935.1 Q142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:150925208 C>A maps to NM_001447.2 E1827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:150925208 C>A maps to NM_001447.2 E1827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:176666860 A>T maps to NM_022455.4 K1433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:176666860 A>T maps to NM_022455.4 K1433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:178410114 G>A maps to NM_000843.3 C744C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr5:178410114 G>A maps to NM_000843.3 C744C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:7569463 G>T maps to NM_004415.2 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:7569463 G>T maps to NM_004415.2 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:26027336 G>A maps to NM_003544.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:26027336 G>A maps to NM_003544.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:29638475 A>G did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:29638475 A>G did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:30166208 C>T maps to NM_003449.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:30166208 C>T maps to NM_003449.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:35438520 A>G maps to NM_007104.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:35438520 A>G maps to NM_007104.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:39855275 C>T maps to ENST00000398904 S656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:39855275 C>T maps to ENST00000398904 S656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:111588222 C>G maps to NM_153369.2 Y486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:111588222 C>G maps to NM_153369.2 Y486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:152702404 C>G maps to NM_182961.2 G2915G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr6:152702404 C>G maps to NM_182961.2 G2915G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr7:31378426 G>A maps to NM_022728.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr7:31378426 G>A maps to NM_022728.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr7:86817561 C>T maps to NM_021145.3 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr7:86817561 C>T maps to NM_021145.3 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr7:103126771 G>T maps to ENST00000428762 T3285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr7:103126771 G>T maps to ENST00000428762 T3285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr7:139030440 G>A maps to NM_197964.3 W111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr7:139030440 G>A maps to NM_197964.3 W111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr7:143573296 T>C maps to NM_014719.1 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr7:143573296 T>C maps to NM_014719.1 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr7:144096937 G>T maps to ENST00000467773 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr7:144096937 G>T maps to ENST00000467773 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr8:8235564 G>C maps to NM_001080826.1 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr8:8235564 G>C maps to NM_001080826.1 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr8:24771548 G>T maps to NM_005382.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr8:24771548 G>T maps to NM_005382.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr8:30889547 G>A maps to NM_013357.2 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr8:30889547 G>A maps to NM_013357.2 R251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr8:52336291 C>G did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr8:52336291 C>G did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr8:68123820 A>G maps to NM_006421.3 I1572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr8:68123820 A>G maps to NM_006421.3 I1572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr8:91937822 C>T maps to NM_022351.4 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr8:91937822 C>T maps to NM_022351.4 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr8:133622459 A>G maps to ENST00000250173 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr8:133622459 A>G maps to ENST00000250173 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr9:5763585 A>G maps to ENST00000414202 T853T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr9:5763585 A>G maps to ENST00000414202 T853T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr9:117848971 G>T maps to NM_002160.2 C346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr9:117848971 G>T maps to NM_002160.2 C346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr9:126776322 G>T maps to NM_004789.3 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr9:126776322 G>T maps to NM_004789.3 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr9:139748461 C>T maps to ENST00000392881 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chr9:139748461 C>T maps to ENST00000392881 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chrX:30260455 C>G maps to NM_002367.3 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chrX:30260455 C>G maps to NM_002367.3 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chrX:129171508 G>A did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chrX:129171508 G>A did not map to a codon.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chrX:140994506 C>T maps to NM_005462.4 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chrX:140994506 C>T maps to NM_005462.4 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chrX:148037157 G>A maps to NM_002025.3 W528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chrX:148037157 G>A maps to NM_002025.3 W528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chrY:16953105 A>T maps to ENST00000382868 T862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5356-01A-01D-1434-08 chrY:16953105 A>T maps to ENST00000382868 T862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr1:23520601 G>C maps to NM_000864.4 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr1:23520601 G>C maps to NM_000864.4 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr10:105176372 C>T maps to NM_014976.1 F548F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr10:105176372 C>T maps to NM_014976.1 F548F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr12:56527376 C>T maps to NM_001184796.1 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr12:56527376 C>T maps to NM_001184796.1 F433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr13:31037727 C>T maps to NM_002128.4 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr13:31037727 C>T maps to NM_002128.4 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr14:21052159 G>T maps to NM_145250.3 C158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr14:21052159 G>T maps to NM_145250.3 C158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr15:40591134 C>T maps to NM_004573.2 K238K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr15:40591134 C>T maps to NM_004573.2 K238K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr16:21136513 G>A maps to NM_017539.1 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr16:21136513 G>A maps to NM_017539.1 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr19:39200968 C>G maps to NM_004924.3 S269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr19:39200968 C>G maps to NM_004924.3 S269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr2:37410657 C>G did not map to a codon.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr2:37410657 C>G did not map to a codon.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr2:86374881 A>G maps to NM_006839.2 D492D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr2:86374881 A>G maps to NM_006839.2 D492D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr2:179436107 G>C maps to NM_133378.4 V22349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr2:179436107 G>C maps to NM_133378.4 V22349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr4:786391 G>A maps to NM_006651.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr4:786391 G>A maps to NM_006651.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr4:38138874 G>A maps to NM_015173.2 T1142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr4:38138874 G>A maps to NM_015173.2 T1142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr4:114279448 C>T maps to NM_001148.4 L3225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr4:114279448 C>T maps to NM_001148.4 L3225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr5:38944563 C>A maps to ENST00000296782 E1657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr5:38944563 C>A maps to ENST00000296782 E1657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr6:150240359 G>C maps to NM_001001788.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr6:150240359 G>C maps to NM_001001788.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr7:88964687 A>T maps to NM_181646.2 K798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr7:88964687 A>T maps to NM_181646.2 K798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr7:92761231 G>T maps to NM_152703.2 Y1351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5358-01A-01D-1512-08 chr7:92761231 G>T maps to NM_152703.2 Y1351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr1:28862413 G>A maps to NM_001048194.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr1:28862413 G>A maps to NM_001048194.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr1:211654484 G>A maps to NM_183059.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr1:211654484 G>A maps to NM_183059.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr1:216348687 A>T maps to ENST00000366943 A1511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr1:216348687 A>T maps to ENST00000366943 A1511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr10:86012691 C>A maps to ENST00000358110 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr10:86012691 C>A maps to ENST00000358110 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr10:118100358 C>A maps to NM_198515.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr10:118100358 C>A maps to NM_198515.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr11:22296149 C>A maps to NM_213599.2 P757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr11:22296149 C>A maps to NM_213599.2 P757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr11:62415547 G>A maps to NM_030628.1 A668A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr11:62415547 G>A maps to NM_030628.1 A668A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr11:78176975 T>C maps to NM_024678.4 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr11:78176975 T>C maps to NM_024678.4 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr11:120352146 C>T maps to NM_015313.2 P1472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr11:120352146 C>T maps to NM_015313.2 P1472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr11:124524554 G>C maps to NM_170601.3 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr11:124524554 G>C maps to NM_170601.3 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr12:6457161 T>C maps to NM_001159576.1 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr12:6457161 T>C maps to NM_001159576.1 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr12:43944861 G>A maps to ENST00000389420 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr12:43944861 G>A maps to ENST00000389420 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr14:50312959 C>T maps to NM_004713.3 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr14:50312959 C>T maps to NM_004713.3 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr14:69256576 A>T maps to NM_004926.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr14:69256576 A>T maps to NM_004926.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr16:16101761 C>T maps to ENST00000399408 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr16:16101761 C>T maps to ENST00000399408 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr16:24192239 C>A maps to NM_002738.6 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr16:24192239 C>A maps to NM_002738.6 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr17:7578246 A>T maps to NM_001126112.1 L201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr17:7578246 A>T maps to NM_001126112.1 L201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr17:8170876 C>T maps to NM_012393.2 D1092D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr17:8170876 C>T maps to NM_012393.2 D1092D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr17:26691846 C>T maps to NM_001080837.2 W80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr17:26691846 C>T maps to NM_001080837.2 W80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr17:26862067 G>T maps to NM_003593.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr17:26862067 G>T maps to NM_003593.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr17:42428418 C>T maps to NM_002087.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr17:42428418 C>T maps to NM_002087.2 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr17:46673815 G>A maps to NM_018952.4 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr17:46673815 G>A maps to NM_018952.4 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr18:14105332 T>C maps to NM_145287.3 K402K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr18:14105332 T>C maps to NM_145287.3 K402K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr18:29110981 C>T maps to NM_001943.3 D349D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr18:29110981 C>T maps to NM_001943.3 D349D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr19:7964964 C>T maps to NM_025061.3 Q520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr19:7964964 C>T maps to NM_025061.3 Q520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr19:33370187 G>A maps to NM_032816.3 G744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr19:33370187 G>A maps to NM_032816.3 G744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr19:55105659 A>T did not map to a codon.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr19:55105659 A>T did not map to a codon.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr19:57985604 C>T maps to NM_001024596.2 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr19:57985604 C>T maps to NM_001024596.2 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr2:24432686 C>T maps to NM_006277.2 T1491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr2:24432686 C>T maps to NM_006277.2 T1491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr2:33784036 C>T maps to NM_170672.2 D668D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr2:33784036 C>T maps to NM_170672.2 D668D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr2:99279520 G>T maps to NM_012214.2 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr2:99279520 G>T maps to NM_012214.2 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr2:175450339 C>T did not map to a codon.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr2:175450339 C>T did not map to a codon.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr20:25205949 G>T maps to NM_001247.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr20:25205949 G>T maps to NM_001247.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr20:45725800 C>T maps to ENST00000360649 Y299Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr20:45725800 C>T maps to ENST00000360649 Y299Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr3:172365793 G>C maps to NM_001146276.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr3:172365793 G>C maps to NM_001146276.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr4:100232741 C>T maps to NM_000668.4 Q300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr4:100232741 C>T maps to NM_000668.4 Q300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr4:100242500 T>A did not map to a codon.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr4:100242500 T>A did not map to a codon.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr4:114209629 C>T maps to NM_001148.4 N755N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr4:114209629 C>T maps to NM_001148.4 N755N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr4:120190942 A>G maps to NM_019050.2 Q462Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr4:120190942 A>G maps to NM_019050.2 Q462Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr4:187541442 G>A maps to ENST00000260147 V2102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr4:187541442 G>A maps to ENST00000260147 V2102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr5:33576464 G>T maps to NM_030955.2 P1222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr5:33576464 G>T maps to NM_030955.2 P1222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr5:71756159 C>T maps to NM_152625.1 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr5:71756159 C>T maps to NM_152625.1 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr5:132158992 G>A maps to NM_001172700.1 R725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr5:132158992 G>A maps to NM_001172700.1 R725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr5:161116007 G>A maps to NM_000811.2 K93K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr5:161116007 G>A maps to NM_000811.2 K93K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr6:46644142 G>A maps to NM_004277.3 W308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr6:46644142 G>A maps to NM_004277.3 W308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr6:57048921 A>G maps to NM_004282.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr6:57048921 A>G maps to NM_004282.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr6:132649649 G>A maps to NM_015529.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr6:132649649 G>A maps to NM_015529.2 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr6:161139389 C>T maps to NM_000301.3 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr6:161139389 C>T maps to NM_000301.3 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr7:50468216 C>T maps to NM_006060.3 H484H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr7:50468216 C>T maps to NM_006060.3 H484H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr7:115624313 A>G did not map to a codon.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr7:115624313 A>G did not map to a codon.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr9:98238314 C>A did not map to a codon.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr9:98238314 C>A did not map to a codon.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr9:119976895 G>T maps to ENST00000313400 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5359-01A-01D-1434-08 chr9:119976895 G>T maps to ENST00000313400 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:11918860 C>A maps to NM_002521.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:11918860 C>A maps to NM_002521.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:111435055 G>T maps to NM_000560.3 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:111435055 G>T maps to NM_000560.3 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:150131288 C>A maps to ENST00000443480 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:150131288 C>A maps to ENST00000443480 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:158815618 C>A maps to NM_002432.1 Y271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:158815618 C>A maps to NM_002432.1 Y271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:175348703 G>A maps to NM_003285.2 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:175348703 G>A maps to NM_003285.2 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:179587801 A>G maps to ENST00000444136 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:179587801 A>G maps to ENST00000444136 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:181690997 C>A maps to ENST00000357570 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:181690997 C>A maps to ENST00000357570 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:196871596 T>C maps to NM_006684.2 Y36Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:196871596 T>C maps to NM_006684.2 Y36Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:200017864 G>T maps to NM_205860.1 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:200017864 G>T maps to NM_205860.1 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:216373029 C>T maps to ENST00000366943 K1250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:216373029 C>T maps to ENST00000366943 K1250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:241094031 C>A maps to ENST00000407727 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:241094031 C>A maps to ENST00000407727 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:242159635 G>A maps to NM_001004343.2 N91N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr1:242159635 G>A maps to NM_001004343.2 N91N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr10:38406774 A>G maps to NM_003421.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr10:38406774 A>G maps to NM_003421.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr10:128974170 G>C maps to NM_001039762.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr10:128974170 G>C maps to NM_001039762.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:1255444 C>A maps to ENST00000447027 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:1255444 C>A maps to ENST00000447027 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:1268009 A>C maps to ENST00000447027 P3303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:1268009 A>C maps to ENST00000447027 P3303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:1269680 A>C maps to ENST00000447027 P3860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:1269680 A>C maps to ENST00000447027 P3860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:5290722 C>A maps to NM_005330.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:5290722 C>A maps to NM_005330.3 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:5411011 C>T maps to NM_001004756.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:5411011 C>T maps to NM_001004756.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:6024018 G>A maps to NM_001005179.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:6024018 G>A maps to NM_001005179.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:22294480 A>T maps to NM_213599.2 I727I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:22294480 A>T maps to NM_213599.2 I727I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:30033430 G>T maps to NM_002233.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:30033430 G>T maps to NM_002233.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:55735897 G>A maps to NM_001005491.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:55735897 G>A maps to NM_001005491.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:56085892 C>A maps to NM_001005202.1 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:56085892 C>A maps to NM_001005202.1 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:56258069 G>A maps to NM_001005282.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:56258069 G>A maps to NM_001005282.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:59622210 T>C maps to NM_001062.3 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:59622210 T>C maps to NM_001062.3 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:68830380 C>A maps to NM_139075.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:68830380 C>A maps to NM_139075.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:99827583 G>T maps to NM_014361.2 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:99827583 G>T maps to NM_014361.2 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:102646042 C>T maps to NM_002425.2 W314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:102646042 C>T maps to NM_002425.2 W314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:124617496 G>A maps to NM_014312.3 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:124617496 G>A maps to NM_014312.3 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:11139066 C>T maps to NM_176890.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:11139066 C>T maps to NM_176890.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:15475701 C>A maps to NM_030667.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:15475701 C>A maps to NM_030667.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:22013988 C>T maps to NM_005691.2 R780R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:22013988 C>T maps to NM_005691.2 R780R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:22676468 C>A maps to ENST00000446597 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:22676468 C>A maps to ENST00000446597 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:55820375 C>T maps to NM_001005183.1 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:55820375 C>T maps to NM_001005183.1 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:104044338 G>T maps to NM_017564.9 G414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:104044338 G>T maps to NM_017564.9 G414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:114793738 G>T maps to NM_000192.3 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:114793738 G>T maps to NM_000192.3 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:133241049 T>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr12:133241049 T>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr13:49033969 G>T did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr13:49033969 G>T did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr14:52433375 G>T maps to NM_053064.3 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr14:52433375 G>T maps to NM_053064.3 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr15:55669216 T>C maps to ENST00000442196 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr15:55669216 T>C maps to ENST00000442196 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr15:58287337 C>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr15:58287337 C>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr15:67873099 C>T maps to NM_145160.1 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr15:67873099 C>T maps to NM_145160.1 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr15:73659939 G>A maps to NM_005477.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr15:73659939 G>A maps to NM_005477.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr15:100269707 T>A maps to NM_152449.2 K172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr15:100269707 T>A maps to NM_152449.2 K172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr16:3614574 G>T maps to ENST00000448023 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr16:3614574 G>T maps to ENST00000448023 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr16:20410586 G>T maps to NM_174924.1 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr16:20410586 G>T maps to NM_174924.1 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr16:20824540 T>C maps to NM_030941.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr16:20824540 T>C maps to NM_030941.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr16:21038392 G>A maps to NM_017539.1 F1832F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr16:21038392 G>A maps to NM_017539.1 F1832F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CN-5360-01A-01D-1434-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CN-5360-01A-01D-1434-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr16:82131824 G>A maps to NM_002153.2 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr16:82131824 G>A maps to NM_002153.2 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr17:27041919 T>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr17:27041919 T>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr17:56344746 G>A maps to NM_006151.2 Q577Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr17:56344746 G>A maps to NM_006151.2 Q577Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr17:57270974 C>A maps to NM_018304.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr17:57270974 C>A maps to NM_018304.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr17:64225440 T>A maps to NM_000042.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr17:64225440 T>A maps to NM_000042.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr18:5891897 G>A maps to NM_001080209.1 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr18:5891897 G>A maps to NM_001080209.1 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr18:11888678 C>T maps to ENST00000344987 W186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr18:11888678 C>T maps to ENST00000344987 W186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr18:40857289 C>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr18:40857289 C>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr18:43329783 G>A maps to NM_001146037.1 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr18:43329783 G>A maps to NM_001146037.1 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr18:54293688 C>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr18:54293688 C>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr18:61066521 C>T maps to NM_004869.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr18:61066521 C>T maps to NM_004869.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:3207204 G>A maps to NM_020170.3 E503E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:3207204 G>A maps to NM_020170.3 E503E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:9088914 C>T maps to NM_024690.2 W967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:9088914 C>T maps to NM_024690.2 W967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:10464799 C>A maps to NM_003331.4 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:10464799 C>A maps to NM_003331.4 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:12542084 T>A maps to NM_005815.4 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:12542084 T>A maps to NM_005815.4 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:15739138 G>T maps to NM_007253.3 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:15739138 G>T maps to NM_007253.3 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:17015050 G>T maps to ENST00000443236 G1469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:17015050 G>T maps to ENST00000443236 G1469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:17394534 G>A maps to NM_152363.4 W321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:17394534 G>A maps to NM_152363.4 W321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:22155423 G>T maps to NM_007153.3 P804P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:22155423 G>T maps to NM_007153.3 P804P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:37118347 G>T maps to NM_032825.3 E517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:37118347 G>T maps to NM_032825.3 E517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:39972551 T>C maps to NM_001001563.1 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:39972551 T>C maps to NM_001001563.1 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:51919977 A>G maps to NM_033130.4 H216H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:51919977 A>G maps to NM_033130.4 H216H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:53740379 G>A maps to NM_182609.2 Q534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:53740379 G>A maps to NM_182609.2 Q534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:56042590 A>G maps to NM_001101401.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:56042590 A>G maps to NM_001101401.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:57641828 G>T maps to NM_020903.2 E596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:57641828 G>T maps to NM_020903.2 E596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:57666724 G>T maps to NM_001012729.1 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr19:57666724 G>T maps to NM_001012729.1 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:11718541 G>T maps to NM_014668.3 G253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:11718541 G>T maps to NM_014668.3 G253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:27480192 C>G maps to NM_003459.4 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:27480192 C>G maps to NM_003459.4 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:105859166 C>T maps to NM_007227.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:105859166 C>T maps to NM_007227.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:113788709 A>G maps to NM_173178.1 Y12Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:113788709 A>G maps to NM_173178.1 Y12Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:128408389 G>A maps to NM_005291.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:128408389 G>A maps to NM_005291.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:141130601 C>A maps to NM_018557.2 G3581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:141130601 C>A maps to NM_018557.2 G3581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:161223857 G>A maps to NM_016836.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:161223857 G>A maps to NM_016836.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:170136934 A>G maps to NM_004525.2 N422N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:170136934 A>G maps to NM_004525.2 N422N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:175326174 G>A maps to NM_152529.5 H505H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:175326174 G>A maps to NM_152529.5 H505H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:190430078 C>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:190430078 C>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:197943432 C>A maps to NM_001195144.1 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:197943432 C>A maps to NM_001195144.1 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:207989095 C>G maps to NM_003709.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:207989095 C>G maps to NM_003709.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:231249969 G>A maps to NM_138402.4 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:231249969 G>A maps to NM_138402.4 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:238296330 G>T maps to NM_004369.3 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr2:238296330 G>T maps to NM_004369.3 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr20:1286352 C>A maps to ENST00000381876 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr20:1286352 C>A maps to ENST00000381876 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr20:25060073 G>A maps to NM_014588.4 H167H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr20:25060073 G>A maps to NM_014588.4 H167H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr20:35154396 C>A maps to ENST00000339266 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr20:35154396 C>A maps to ENST00000339266 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr22:37273816 G>C maps to NM_000631.4 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr22:37273816 G>C maps to NM_000631.4 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr22:50962504 C>G maps to NM_001169111.1 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr22:50962504 C>G maps to NM_001169111.1 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:14755663 C>A maps to NM_032137.4 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:14755663 C>A maps to NM_032137.4 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:15300344 G>A maps to NM_004844.3 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:15300344 G>A maps to NM_004844.3 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:38921581 G>T maps to ENST00000302328 P1084P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:38921581 G>T maps to ENST00000302328 P1084P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:42132990 C>G maps to NM_001042646.1 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:42132990 C>G maps to NM_001042646.1 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:52977587 C>A maps to NM_016329.3 G49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:52977587 C>A maps to NM_016329.3 G49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:97868306 C>A maps to NM_001005514.1 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:97868306 C>A maps to NM_001005514.1 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:108822765 T>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:108822765 T>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:122247276 T>C maps to NM_031458.2 S833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:122247276 T>C maps to NM_031458.2 S833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:140281732 C>A maps to NM_022131.2 R765R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:140281732 C>A maps to NM_022131.2 R765R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:147131167 C>T maps to NM_003412.3 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:147131167 C>T maps to NM_003412.3 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:147131265 C>A maps to NM_003412.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:147131265 C>A maps to NM_003412.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:159711263 G>A maps to NM_000882.2 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:159711263 G>A maps to NM_000882.2 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:160037640 A>G maps to ENST00000483754 C459C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:160037640 A>G maps to ENST00000483754 C459C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:172046815 G>T maps to NM_022763.3 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:172046815 G>T maps to NM_022763.3 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:182987804 C>T maps to NM_032047.4 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:182987804 C>T maps to NM_032047.4 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:183824075 C>A maps to NM_182589.2 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:183824075 C>A maps to NM_182589.2 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:194336359 T>A maps to NM_001166305.1 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:194336359 T>A maps to NM_001166305.1 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:197665492 C>T maps to NM_001134435.1 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr3:197665492 C>T maps to NM_001134435.1 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:2306179 G>T maps to NM_020972.2 P629P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:2306179 G>T maps to NM_020972.2 P629P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:71275726 C>T maps to NM_021225.4 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:71275726 C>T maps to NM_021225.4 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:77283401 C>A maps to NM_001042784.1 E633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:77283401 C>A maps to NM_001042784.1 E633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:85600084 G>A maps to NM_014991.4 S3378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:85600084 G>A maps to NM_014991.4 S3378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:111397695 G>A maps to NM_001977.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:111397695 G>A maps to NM_001977.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:121828687 C>A maps to NM_018699.2 G40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:121828687 C>A maps to NM_018699.2 G40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:166910617 C>A maps to ENST00000507499 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:166910617 C>A maps to ENST00000507499 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:186295606 C>T maps to ENST00000362004 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr4:186295606 C>T maps to ENST00000362004 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:3600252 C>T maps to NM_024337.3 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:3600252 C>T maps to NM_024337.3 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:13692193 G>T maps to NM_001369.2 R4592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:13692193 G>T maps to NM_001369.2 R4592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:41000407 G>A maps to ENST00000296803 Q1467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:41000407 G>A maps to ENST00000296803 Q1467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:74017518 A>G maps to NM_032380.3 D767D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:74017518 A>G maps to NM_032380.3 D767D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:140176057 G>T maps to NM_018905.2 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:140176057 G>T maps to NM_018905.2 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:140229948 C>T maps to NM_031857.1 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:140229948 C>T maps to NM_031857.1 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:140236299 G>T maps to NM_018901.2 G223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:140236299 G>T maps to NM_018901.2 G223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:140250826 G>T maps to NM_018902.3 T713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:140250826 G>T maps to NM_018902.3 T713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:140772326 A>G did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:140772326 A>G did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:150712871 G>A maps to NM_181776.2 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:150712871 G>A maps to NM_181776.2 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:170720912 T>A maps to NM_022897.3 I990I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:170720912 T>A maps to NM_022897.3 I990I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:176637630 C>G maps to NM_022455.4 S744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr5:176637630 C>G maps to NM_022455.4 S744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:17539516 A>G maps to NM_006366.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:17539516 A>G maps to NM_006366.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:38754682 G>A maps to ENST00000327475 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:38754682 G>A maps to ENST00000327475 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:49754393 T>C maps to NM_138733.4 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:49754393 T>C maps to NM_138733.4 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:76624543 G>T maps to ENST00000428345 E1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:76624543 G>T maps to ENST00000428345 E1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:90402455 C>T maps to NM_014611.1 R3431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:90402455 C>T maps to NM_014611.1 R3431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:127471640 A>G maps to ENST00000368317 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:127471640 A>G maps to ENST00000368317 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:132271471 G>A maps to NM_001901.2 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:132271471 G>A maps to NM_001901.2 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:155450863 G>T maps to ENST00000456144 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr6:155450863 G>T maps to ENST00000456144 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:20762763 C>T maps to NM_001163941.1 A849A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:20762763 C>T maps to NM_001163941.1 A849A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:70881050 T>C did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:70881050 T>C did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:82579580 C>A maps to NM_033026.5 V3441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:82579580 C>A maps to NM_033026.5 V3441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:97822446 T>C maps to NM_014916.3 S890S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:97822446 T>C maps to NM_014916.3 S890S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:105190712 A>G maps to NM_021930.4 E371E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:105190712 A>G maps to NM_021930.4 E371E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:106822944 A>G maps to NM_012257.3 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:106822944 A>G maps to NM_012257.3 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:123152339 C>A maps to NM_178827.4 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:123152339 C>A maps to NM_178827.4 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:124499082 G>A maps to NM_015450.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:124499082 G>A maps to NM_015450.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:132193308 G>T maps to NM_020911.1 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:132193308 G>T maps to NM_020911.1 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:138261115 A>T did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:138261115 A>T did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:150696316 C>A maps to NM_000603.4 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr7:150696316 C>A maps to NM_000603.4 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr8:1513940 C>T maps to ENST00000357934 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr8:1513940 C>T maps to ENST00000357934 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr8:13357322 G>A maps to NM_182643.2 D86D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr8:13357322 G>A maps to NM_182643.2 D86D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr8:53451005 G>C maps to NM_207413.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr8:53451005 G>C maps to NM_207413.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr8:54142036 G>T maps to NM_000912.3 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr8:54142036 G>T maps to NM_000912.3 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr8:86114379 A>T did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr8:86114379 A>T did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr8:144681056 G>T maps to NM_032862.4 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr8:144681056 G>T maps to NM_032862.4 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr9:72459431 G>T did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr9:72459431 G>T did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr9:113261432 C>T maps to ENST00000374463 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr9:113261432 C>T maps to ENST00000374463 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr9:135602854 T>A maps to NM_152572.2 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr9:135602854 T>A maps to NM_152572.2 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr9:137653805 G>C maps to NM_000093.3 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr9:137653805 G>C maps to NM_000093.3 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr9:139889997 G>A maps to NM_004669.2 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr9:139889997 G>A maps to NM_004669.2 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chrX:15349560 C>G maps to NM_002641.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chrX:15349560 C>G maps to NM_002641.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chrX:29414434 A>T maps to NM_014271.3 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chrX:29414434 A>T maps to NM_014271.3 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chrX:30269233 C>A maps to NM_177404.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chrX:30269233 C>A maps to NM_177404.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chrX:73963449 A>G maps to NM_001008537.2 Y314Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chrX:73963449 A>G maps to NM_001008537.2 Y314Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chrX:84258907 G>T did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chrX:84258907 G>T did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chrX:90691136 G>T maps to NM_080832.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chrX:90691136 G>T maps to NM_080832.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chrX:140994308 C>A maps to NM_005462.4 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chrX:140994308 C>A maps to NM_005462.4 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chrX:144337279 C>A maps to NM_001009614.2 C55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chrX:144337279 C>A maps to NM_001009614.2 C55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chrX:153134315 C>A maps to NM_000425.3 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chrX:153134315 C>A maps to NM_000425.3 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr1:9787004 G>A maps to ENST00000361110 L1036L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr1:9787004 G>A maps to ENST00000361110 L1036L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr1:64515513 C>T maps to NM_005012.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr1:64515513 C>T maps to NM_005012.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr1:113189887 A>C maps to NM_006135.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr1:113189887 A>C maps to NM_006135.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr1:196967389 C>G maps to ENST00000367414 S392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr1:196967389 C>G maps to ENST00000367414 S392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr1:230846410 G>C maps to NM_000029.3 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr1:230846410 G>C maps to NM_000029.3 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr10:73553320 C>A maps to ENST00000398860 V2217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr10:73553320 C>A maps to ENST00000398860 V2217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr10:93390208 G>A maps to NM_005398.4 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr10:93390208 G>A maps to NM_005398.4 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr11:67261027 G>A maps to NM_004910.2 V1065V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr11:67261027 G>A maps to NM_004910.2 V1065V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr11:68696780 G>A maps to NM_002180.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr11:68696780 G>A maps to NM_002180.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr12:20833103 C>T maps to NM_000921.3 Q1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr12:20833103 C>T maps to NM_000921.3 Q1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr13:101759853 G>A maps to NM_052867.2 R855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr13:101759853 G>A maps to NM_052867.2 R855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr14:24607451 C>G maps to NM_176783.1 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr14:24607451 C>G maps to NM_176783.1 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr14:61857998 C>T maps to NM_006255.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr14:61857998 C>T maps to NM_006255.3 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr15:41145415 C>A maps to NM_181642.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr15:41145415 C>A maps to NM_181642.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr15:69011052 C>T maps to NM_006091.3 H328H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr15:69011052 C>T maps to NM_006091.3 H328H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr15:90176167 C>T maps to NM_198525.2 R926R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr15:90176167 C>T maps to NM_198525.2 R926R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr16:2762695 G>A maps to NM_031948.3 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr16:2762695 G>A maps to NM_031948.3 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr16:23700658 C>T maps to NM_005030.3 D457D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr16:23700658 C>T maps to NM_005030.3 D457D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr16:88691021 G>A maps to ENST00000452588 V661V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr16:88691021 G>A maps to ENST00000452588 V661V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr17:17716990 C>T maps to NM_001005291.2 Q1028Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr17:17716990 C>T maps to NM_001005291.2 Q1028Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr19:15350542 G>A maps to NM_058243.2 P1124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr19:15350542 G>A maps to NM_058243.2 P1124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr19:40367903 G>T maps to NM_003890.2 C4352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr19:40367903 G>T maps to NM_003890.2 C4352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr19:42128133 G>A maps to NM_001817.2 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr19:42128133 G>A maps to NM_001817.2 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr19:51227676 G>C maps to NM_002975.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr19:51227676 G>C maps to NM_002975.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr19:54664093 G>C maps to NM_001145303.1 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr19:54664093 G>C maps to NM_001145303.1 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr2:61597671 A>G maps to NM_014709.3 N373N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr2:61597671 A>G maps to NM_014709.3 N373N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr2:161030574 G>A maps to NM_000888.3 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr2:161030574 G>A maps to NM_000888.3 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr2:179476144 G>A maps to NM_133378.4 S14369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr2:179476144 G>A maps to NM_133378.4 S14369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr2:238253400 C>G maps to NM_004369.3 R2420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr2:238253400 C>G maps to NM_004369.3 R2420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr20:36850903 G>T maps to NM_001029864.1 T788T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr20:36850903 G>T maps to NM_001029864.1 T788T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr20:47752435 G>C maps to NM_017453.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr20:47752435 G>C maps to NM_017453.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr22:44234791 G>A maps to NM_014351.3 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr22:44234791 G>A maps to NM_014351.3 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr22:50962768 C>T maps to NM_001169111.1 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr22:50962768 C>T maps to NM_001169111.1 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr3:38888754 C>A maps to ENST00000302328 V1602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr3:38888754 C>A maps to ENST00000302328 V1602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr3:48626134 G>A maps to NM_000094.3 R843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr3:48626134 G>A maps to NM_000094.3 R843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr3:189526080 G>T maps to NM_003722.4 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr3:189526080 G>T maps to NM_003722.4 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr3:196434582 T>A maps to NM_032898.3 K115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr3:196434582 T>A maps to NM_032898.3 K115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr4:85731059 T>A maps to NM_014991.4 V775V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr4:85731059 T>A maps to NM_014991.4 V775V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr4:104511030 G>A maps to NM_001059.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr4:104511030 G>A maps to NM_001059.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr5:11384810 G>C maps to NM_001332.2 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr5:11384810 G>C maps to NM_001332.2 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr5:45396671 G>C maps to NM_021072.2 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr5:45396671 G>C maps to NM_021072.2 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr5:176396608 G>T maps to ENST00000377219 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr5:176396608 G>T maps to ENST00000377219 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr6:27925494 G>A maps to NM_012367.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr6:27925494 G>A maps to NM_012367.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr6:56999544 C>T maps to NM_001031623.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr6:56999544 C>T maps to NM_001031623.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr6:63990489 A>G maps to NM_016571.2 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr6:63990489 A>G maps to NM_016571.2 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr6:76527374 A>G maps to ENST00000428345 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr6:76527374 A>G maps to ENST00000428345 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr6:87969023 C>T maps to NM_015021.1 Q1893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr6:87969023 C>T maps to NM_015021.1 Q1893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr6:152129445 G>A maps to NM_001122741.1 E133E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr6:152129445 G>A maps to NM_001122741.1 E133E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr7:44715627 C>A maps to ENST00000444676 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr7:44715627 C>A maps to ENST00000444676 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr7:47385790 G>C maps to NM_022748.11 V815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr7:47385790 G>C maps to NM_022748.11 V815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr7:142460801 G>A maps to ENST00000486171 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr7:142460801 G>A maps to ENST00000486171 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr7:158454899 G>A maps to NM_017760.5 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr7:158454899 G>A maps to NM_017760.5 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr8:101153459 A>T maps to NM_001029860.3 L341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr8:101153459 A>T maps to NM_001029860.3 L341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr8:144358772 C>T maps to NM_138465.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr8:144358772 C>T maps to NM_138465.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr9:140128316 C>A maps to NM_080877.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5361-01A-01D-1434-08 chr9:140128316 C>A maps to NM_080877.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:2938693 C>T maps to NM_080431.4 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:2938693 C>T maps to NM_080431.4 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:17263290 G>A maps to NM_014675.3 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:17263290 G>A maps to NM_014675.3 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:70555456 T>C maps to NM_020794.2 S1462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:70555456 T>C maps to NM_020794.2 S1462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:117208930 C>G maps to NM_001542.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:117208930 C>G maps to NM_001542.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:152800040 A>C maps to NM_178348.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:152800040 A>C maps to NM_178348.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:176668317 G>A maps to NM_020318.2 T943T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:176668317 G>A maps to NM_020318.2 T943T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:183093838 C>T maps to NM_002293.3 C825C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:183093838 C>T maps to NM_002293.3 C825C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:237758917 A>T maps to NM_001035.2 T1519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr1:237758917 A>T maps to NM_001035.2 T1519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr10:95791309 G>A maps to ENST00000371380 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr10:95791309 G>A maps to ENST00000371380 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr10:124339304 C>A maps to ENST00000368915 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr10:124339304 C>A maps to ENST00000368915 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr10:124351998 T>A maps to ENST00000368915 V796V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr10:124351998 T>A maps to ENST00000368915 V796V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr11:5730847 C>T maps to NM_006074.4 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr11:5730847 C>T maps to NM_006074.4 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr12:27467946 G>A did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr12:27467946 G>A did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr12:49883255 G>C maps to NM_023071.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr12:49883255 G>C maps to NM_023071.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr12:120195318 G>C maps to ENST00000392521 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr12:120195318 G>C maps to ENST00000392521 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr12:129694086 G>T maps to NM_133448.2 S474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr12:129694086 G>T maps to NM_133448.2 S474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr13:49281381 C>T maps to NM_020377.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr13:49281381 C>T maps to NM_020377.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr13:58208416 C>T maps to NM_001040429.2 N579N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr13:58208416 C>T maps to NM_001040429.2 N579N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr14:29237741 C>T maps to NM_005249.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr14:29237741 C>T maps to NM_005249.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr14:39517934 T>A did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr14:39517934 T>A did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr14:76249856 C>T maps to NM_015072.4 P990P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr14:76249856 C>T maps to NM_015072.4 P990P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr14:80328090 C>T maps to NM_004796.4 V990V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr14:80328090 C>T maps to NM_004796.4 V990V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr15:29386516 G>T did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr15:29386516 G>T did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr16:50332900 G>C maps to NM_001114.3 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr16:50332900 G>C maps to NM_001114.3 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr16:57597827 C>T maps to ENST00000349457 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr16:57597827 C>T maps to ENST00000349457 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr16:65026866 C>A maps to NM_001797.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr16:65026866 C>A maps to NM_001797.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr16:70863518 A>T did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr16:70863518 A>T did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr17:19315864 G>T maps to NM_007148.4 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr17:19315864 G>T maps to NM_007148.4 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr17:28601108 A>T maps to NM_000386.2 L251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr17:28601108 A>T maps to NM_000386.2 L251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr17:31267869 G>A maps to NM_015544.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr17:31267869 G>A maps to NM_015544.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr17:34308414 G>A maps to NM_004590.2 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr17:34308414 G>A maps to NM_004590.2 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr17:41246659 T>C maps to ENST00000471181 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr17:41246659 T>C maps to ENST00000471181 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr17:48278850 C>A maps to NM_000088.3 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr17:48278850 C>A maps to NM_000088.3 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr18:74154629 C>A maps to ENST00000443185 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr18:74154629 C>A maps to ENST00000443185 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr19:19822313 A>T maps to NM_021030.2 C592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr19:19822313 A>T maps to NM_021030.2 C592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr19:50412641 C>T maps to NM_012346.4 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr19:50412641 C>T maps to NM_012346.4 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr19:56733087 G>A maps to NM_024303.1 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr19:56733087 G>A maps to NM_024303.1 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:50847322 T>A did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:50847322 T>A did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:61508320 C>T maps to NM_014709.3 L1685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:61508320 C>T maps to NM_014709.3 L1685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:79254985 T>C maps to NM_001008387.1 N129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:79254985 T>C maps to NM_001008387.1 N129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:98828425 A>T maps to NM_144992.4 K591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:98828425 A>T maps to NM_144992.4 K591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:166848384 C>T maps to NM_001165963.1 L1800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:166848384 C>T maps to NM_001165963.1 L1800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:169699617 C>T maps to NM_001171631.1 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:169699617 C>T maps to NM_001171631.1 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:220312734 C>T maps to NM_005876.4 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:220312734 C>T maps to NM_005876.4 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:234465563 C>A maps to NM_018218.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr2:234465563 C>A maps to NM_018218.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr3:93781973 C>T maps to NM_022072.3 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr3:93781973 C>T maps to NM_022072.3 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr3:108403091 G>C maps to NM_014648.3 V971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr3:108403091 G>C maps to NM_014648.3 V971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr3:121340296 C>A maps to NM_016298.3 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr3:121340296 C>A maps to NM_016298.3 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr3:156411958 A>T maps to NM_015508.4 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr3:156411958 A>T maps to NM_015508.4 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr3:164905717 G>A maps to NM_014926.2 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr3:164905717 G>A maps to NM_014926.2 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr3:186358266 C>T maps to NM_014375.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr3:186358266 C>T maps to NM_014375.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr4:147561056 C>A maps to NM_004575.2 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr4:147561056 C>A maps to NM_004575.2 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr4:190876257 T>C maps to NM_004477.2 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr4:190876257 T>C maps to NM_004477.2 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr5:1089144 C>T maps to NM_006598.2 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr5:1089144 C>T maps to NM_006598.2 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr5:13716598 G>T maps to NM_001369.2 I4302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr5:13716598 G>T maps to NM_001369.2 I4302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr5:13841179 A>G maps to NM_001369.2 N1848N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr5:13841179 A>G maps to NM_001369.2 N1848N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr5:112917311 G>T maps to NM_022828.3 E1185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr5:112917311 G>T maps to NM_022828.3 E1185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr5:140214168 G>T maps to NM_018910.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr5:140214168 G>T maps to NM_018910.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr5:140720646 C>T maps to NM_018915.2 V703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr5:140720646 C>T maps to NM_018915.2 V703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr5:140777699 G>A maps to NM_018925.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr5:140777699 G>A maps to NM_018925.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:27424700 C>T did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:27424700 C>T did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:28473518 C>A maps to NM_182701.1 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:28473518 C>A maps to NM_182701.1 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:31110479 G>A maps to NM_001105564.1 V835V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:31110479 G>A maps to NM_001105564.1 V835V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:32797313 C>G did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:32797313 C>G did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:42231258 C>A maps to NM_033502.2 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:42231258 C>A maps to NM_033502.2 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:43306785 C>A maps to NM_014345.2 L1650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:43306785 C>A maps to NM_014345.2 L1650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:78172871 C>A maps to NM_000863.1 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:78172871 C>A maps to NM_000863.1 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:146267450 C>T maps to ENST00000367503 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr6:146267450 C>T maps to ENST00000367503 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr7:55874868 G>A maps to NM_207366.2 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr7:55874868 G>A maps to NM_207366.2 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr7:100839227 T>A maps to NM_178176.2 *342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr7:100839227 T>A maps to NM_178176.2 *342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr7:101839912 G>A did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr7:101839912 G>A did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr7:117407110 A>C did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr7:117407110 A>C did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr7:121699857 C>T maps to NM_002851.2 H2241H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr7:121699857 C>T maps to NM_002851.2 H2241H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr7:134635183 A>G maps to NM_033138.3 K618K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr7:134635183 A>G maps to NM_033138.3 K618K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr8:133723205 A>G did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr8:133723205 A>G did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr9:35717215 A>T maps to NM_006289.3 A795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr9:35717215 A>T maps to NM_006289.3 A795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr9:114289920 A>G maps to NM_133464.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr9:114289920 A>G maps to NM_133464.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr9:131140338 C>T maps to NM_001135947.1 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr9:131140338 C>T maps to NM_001135947.1 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chrX:9728792 C>T maps to ENST00000380929 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chrX:9728792 C>T maps to ENST00000380929 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:16203018 C>A maps to NM_015001.2 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:16203018 C>A maps to NM_015001.2 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:27427042 C>A maps to NM_003047.3 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:27427042 C>A maps to NM_003047.3 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:32745440 G>A did not map to a codon.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:32745440 G>A did not map to a codon.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:94037257 G>C maps to NM_003567.2 S648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:94037257 G>C maps to NM_003567.2 S648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:102270140 G>A maps to ENST00000338858 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:102270140 G>A maps to ENST00000338858 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:151734859 C>A maps to NM_031420.2 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:151734859 C>A maps to NM_031420.2 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:186039756 C>T maps to NM_031935.2 I2669I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:186039756 C>T maps to NM_031935.2 I2669I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr11:47594880 C>T maps to NM_018095.4 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr11:47594880 C>T maps to NM_018095.4 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr11:63990912 G>A maps to NM_178443.2 E651E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr11:63990912 G>A maps to NM_178443.2 E651E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr11:66192179 G>T maps to NM_178864.3 E607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr11:66192179 G>T maps to NM_178864.3 E607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr13:99476723 G>C maps to ENST00000428223 V1686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr13:99476723 G>C maps to ENST00000428223 V1686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr14:47504385 C>A maps to NM_001113498.2 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr14:47504385 C>A maps to NM_001113498.2 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr14:100615442 G>A maps to NM_206918.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr14:100615442 G>A maps to NM_206918.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr15:65555577 C>T maps to NM_017851.4 W200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr15:65555577 C>T maps to NM_017851.4 W200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr16:772478 C>T maps to NM_023933.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr16:772478 C>T maps to NM_023933.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr18:21745030 C>T maps to NM_080597.2 T916T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr18:21745030 C>T maps to NM_080597.2 T916T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr19:57723538 C>T maps to NM_003417.4 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr19:57723538 C>T maps to NM_003417.4 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr2:24009038 A>T maps to NM_017552.1 L944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr2:24009038 A>T maps to NM_017552.1 L944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr2:97779538 C>T maps to NM_001164315.1 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr2:97779538 C>T maps to NM_001164315.1 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr2:149247785 C>T maps to ENST00000404807 R1529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr2:149247785 C>T maps to ENST00000404807 R1529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr2:167141151 C>T maps to ENST00000303354 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr2:167141151 C>T maps to ENST00000303354 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr2:187455217 C>T maps to NM_002210.3 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr2:187455217 C>T maps to NM_002210.3 F51F. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CN-5364-01A-01D-1434-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-CN-5364-01A-01D-1434-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr3:185191116 C>T maps to NM_004721.3 C666C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr3:185191116 C>T maps to NM_004721.3 C666C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr3:188590461 G>T maps to NM_005578.3 E541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr3:188590461 G>T maps to NM_005578.3 E541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr4:115767137 G>A maps to NM_022569.1 F652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr4:115767137 G>A maps to NM_022569.1 F652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr4:170042097 T>C maps to NM_020870.3 E463E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr4:170042097 T>C maps to NM_020870.3 E463E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr4:175710092 A>G maps to NM_006529.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr4:175710092 A>G maps to NM_006529.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr5:112458452 G>A maps to NM_001085377.1 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr5:112458452 G>A maps to NM_001085377.1 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr5:140167197 G>T maps to NM_018900.2 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr5:140167197 G>T maps to NM_018900.2 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr6:94120845 G>A maps to NM_004440.3 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr6:94120845 G>A maps to NM_004440.3 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr6:134323169 G>T maps to NM_145176.2 C555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr6:134323169 G>T maps to NM_145176.2 C555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr7:26779554 T>C maps to NM_003930.3 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr7:26779554 T>C maps to NM_003930.3 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr7:50513221 G>A maps to NM_022116.3 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr7:50513221 G>A maps to NM_022116.3 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr7:80439969 G>A maps to NM_006379.2 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr7:80439969 G>A maps to NM_006379.2 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr8:10467545 C>T maps to NM_178857.5 A1354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr8:10467545 C>T maps to NM_178857.5 A1354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr9:86153020 C>A maps to NM_174938.4 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr9:86153020 C>A maps to NM_174938.4 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr9:115760232 C>A maps to NM_001101338.1 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr9:115760232 C>A maps to NM_001101338.1 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr9:138377933 C>T maps to NM_014811.3 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr9:138377933 C>T maps to NM_014811.3 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chrX:63411780 T>C maps to NM_152424.3 E462E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chrX:63411780 T>C maps to NM_152424.3 E462E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr1:66379017 G>T maps to NM_001037341.1 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr1:66379017 G>T maps to NM_001037341.1 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr1:110211612 T>A did not map to a codon.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr1:110211612 T>A did not map to a codon.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr10:124800143 G>T maps to NM_001609.3 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr10:124800143 G>T maps to NM_001609.3 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr12:120651734 T>C maps to NM_001080855.1 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr12:120651734 T>C maps to NM_001080855.1 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr13:67802499 C>A maps to NM_203487.2 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr13:67802499 C>A maps to NM_203487.2 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr14:105412487 G>A maps to NM_138420.2 P3100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr14:105412487 G>A maps to NM_138420.2 P3100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr17:36997561 G>A maps to NM_001080465.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr17:36997561 G>A maps to NM_001080465.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr17:37922444 G>A maps to NM_012481.3 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr17:37922444 G>A maps to NM_012481.3 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr17:56429451 G>A maps to NM_003168.1 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr17:56429451 G>A maps to NM_003168.1 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr17:60657495 T>C maps to ENST00000326270 N459N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr17:60657495 T>C maps to ENST00000326270 N459N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr2:150426655 A>T maps to NM_015702.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr2:150426655 A>T maps to NM_015702.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr2:152580788 G>C maps to NM_001164507.1 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr2:152580788 G>C maps to NM_001164507.1 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr2:172309701 G>T maps to NM_025000.3 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr2:172309701 G>T maps to NM_025000.3 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr2:232263353 C>T maps to NM_145236.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr2:232263353 C>T maps to NM_145236.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr3:123633808 C>T maps to NM_022757.4 V852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr3:123633808 C>T maps to NM_022757.4 V852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr3:155301386 C>T maps to ENST00000340059 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr3:155301386 C>T maps to ENST00000340059 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr4:42145871 G>A maps to NM_207406.3 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr4:42145871 G>A maps to NM_207406.3 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr5:39110491 C>G did not map to a codon.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr5:39110491 C>G did not map to a codon.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr5:79734564 C>T maps to NM_014733.3 I687I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr5:79734564 C>T maps to NM_014733.3 I687I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr5:96503520 C>G maps to NM_018343.2 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr5:96503520 C>G maps to NM_018343.2 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr5:133326806 G>C maps to NM_003374.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr5:133326806 G>C maps to NM_003374.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr6:30954440 C>T maps to NM_001010909.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr6:30954440 C>T maps to NM_001010909.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr6:46802420 C>G maps to NM_005588.2 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr6:46802420 C>G maps to NM_005588.2 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr7:11464387 G>A maps to ENST00000423059 I1106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr7:11464387 G>A maps to ENST00000423059 I1106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr7:83590839 G>A maps to NM_006080.2 F721F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr7:83590839 G>A maps to NM_006080.2 F721F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr9:139413946 G>A maps to NM_017617.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5365-01A-01D-1434-08 chr9:139413946 G>A maps to NM_017617.3 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr1:11985514 G>A maps to ENST00000376576 H260H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr1:11985514 G>A maps to ENST00000376576 H260H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr1:40434297 G>A maps to NM_001136493.1 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr1:40434297 G>A maps to NM_001136493.1 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr1:154303597 T>A maps to NM_020452.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr1:154303597 T>A maps to NM_020452.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr10:68688014 G>C maps to NM_178011.3 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr10:68688014 G>C maps to NM_178011.3 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr10:127412502 C>T maps to ENST00000356792 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr10:127412502 C>T maps to ENST00000356792 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr11:65792842 G>A maps to NM_053054.3 H336H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr11:65792842 G>A maps to NM_053054.3 H336H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr11:71185568 C>T maps to NM_018161.4 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr11:71185568 C>T maps to NM_018161.4 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr12:25308246 G>A maps to NM_018272.3 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr12:25308246 G>A maps to NM_018272.3 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr12:52994828 G>A maps to NM_080747.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr12:52994828 G>A maps to NM_080747.2 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr12:57106905 G>C maps to NM_001113203.1 V2013V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr12:57106905 G>C maps to NM_001113203.1 V2013V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr15:101120723 G>A maps to NM_001040616.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr15:101120723 G>A maps to NM_001040616.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr16:68021882 G>A maps to NM_022355.2 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr16:68021882 G>A maps to NM_022355.2 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr17:26885584 C>A maps to NM_033198.3 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr17:26885584 C>A maps to NM_033198.3 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr18:63526221 C>T maps to NM_004361.2 N478N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr18:63526221 C>T maps to NM_004361.2 N478N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr19:2834411 A>T maps to NM_001102651.1 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr19:2834411 A>T maps to NM_001102651.1 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr19:8387791 A>T maps to NM_198471.2 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr19:8387791 A>T maps to NM_198471.2 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr19:21910042 G>A maps to NM_173531.3 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr19:21910042 G>A maps to NM_173531.3 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr19:44471150 C>A maps to NM_013359.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr19:44471150 C>A maps to NM_013359.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr2:11780420 G>A maps to NM_014668.3 A1897A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr2:11780420 G>A maps to NM_014668.3 A1897A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr22:24982182 G>A maps to NM_207644.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr22:24982182 G>A maps to NM_207644.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr22:39411611 G>A maps to ENST00000396762 K32K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr22:39411611 G>A maps to ENST00000396762 K32K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr3:126255197 T>C did not map to a codon.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr3:126255197 T>C did not map to a codon.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr3:164907435 G>A maps to NM_014926.2 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr3:164907435 G>A maps to NM_014926.2 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr4:106156861 C>A maps to ENST00000513237 S609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr4:106156861 C>A maps to ENST00000513237 S609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr4:115997943 G>A maps to NM_022569.1 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr4:115997943 G>A maps to NM_022569.1 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr5:13883147 G>A maps to NM_001369.2 S1013S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr5:13883147 G>A maps to NM_001369.2 S1013S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr5:40958325 G>A maps to NM_000587.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr5:40958325 G>A maps to NM_000587.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr6:75829168 G>A maps to ENST00000322507 S2369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr6:75829168 G>A maps to ENST00000322507 S2369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr6:139563751 G>A maps to ENST00000358430 R656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr6:139563751 G>A maps to ENST00000358430 R656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr6:169632833 G>A maps to NM_003247.2 C619C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr6:169632833 G>A maps to NM_003247.2 C619C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr7:94052390 C>T maps to NM_000089.3 F842F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr7:94052390 C>T maps to NM_000089.3 F842F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr7:126410116 G>A maps to NM_001127323.1 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr7:126410116 G>A maps to NM_001127323.1 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr8:144940257 G>A maps to NM_031308.1 D2388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chr8:144940257 G>A maps to NM_031308.1 D2388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chrX:73962240 G>C maps to NM_001008537.2 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5366-01A-01D-1434-08 chrX:73962240 G>C maps to NM_001008537.2 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr1:156876576 T>A maps to NM_001080471.1 Y183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr1:156876576 T>A maps to NM_001080471.1 Y183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr1:232942445 T>C maps to NM_019090.2 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr1:232942445 T>C maps to NM_019090.2 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr10:95287807 T>C maps to NM_018131.4 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr10:95287807 T>C maps to NM_018131.4 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr11:7960500 A>G maps to NM_001003745.1 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr11:7960500 A>G maps to NM_001003745.1 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr11:14853184 G>C did not map to a codon.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr11:14853184 G>C did not map to a codon.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr11:61097014 G>T maps to NM_001923.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr11:61097014 G>T maps to NM_001923.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr11:106681088 G>C maps to ENST00000282249 S441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr11:106681088 G>C maps to ENST00000282249 S441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr11:117695378 C>T maps to NM_001127489.1 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr11:117695378 C>T maps to NM_001127489.1 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr14:67671508 G>A maps to NM_173526.3 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr14:67671508 G>A maps to NM_173526.3 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr14:71444273 C>G maps to NM_014982.2 S407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr14:71444273 C>G maps to NM_014982.2 S407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr15:49663514 G>C maps to NM_152647.2 S365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr15:49663514 G>C maps to NM_152647.2 S365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr15:64067316 A>C maps to ENST00000261887 L169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr15:64067316 A>C maps to ENST00000261887 L169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr16:7568363 C>T maps to NM_145891.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr16:7568363 C>T maps to NM_145891.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr16:65016075 A>G maps to NM_001797.2 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr16:65016075 A>G maps to NM_001797.2 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr16:67265093 G>A maps to NM_013241.2 A888A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr16:67265093 G>A maps to NM_013241.2 A888A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr17:34893087 G>A maps to NM_178517.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr17:34893087 G>A maps to NM_178517.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr19:31040059 C>T maps to NM_014717.1 N1178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr19:31040059 C>T maps to NM_014717.1 N1178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr20:9388619 T>C maps to NM_001172646.1 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr20:9388619 T>C maps to NM_001172646.1 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr20:21143677 C>A maps to NM_018474.4 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr20:21143677 C>A maps to NM_018474.4 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr3:51746778 C>T maps to NM_000839.3 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr3:51746778 C>T maps to NM_000839.3 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr3:133486975 A>G maps to NM_001063.3 K530K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr3:133486975 A>G maps to NM_001063.3 K530K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr3:182759448 A>C maps to NM_020166.3 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr3:182759448 A>C maps to NM_020166.3 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr4:6925211 C>T maps to NM_001113361.1 H32H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr4:6925211 C>T maps to NM_001113361.1 H32H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr4:17583957 A>G maps to NM_015907.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr4:17583957 A>G maps to NM_015907.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr5:134724630 G>A maps to NM_138610.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr5:134724630 G>A maps to NM_138610.2 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr5:140755359 C>T maps to NM_018919.2 D570D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr5:140755359 C>T maps to NM_018919.2 D570D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr5:154179560 G>T maps to ENST00000377643 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr5:154179560 G>T maps to ENST00000377643 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr6:27101003 C>T maps to NM_021064.4 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr6:27101003 C>T maps to NM_021064.4 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr6:28294188 G>A maps to NM_030899.4 C325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr6:28294188 G>A maps to NM_030899.4 C325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr6:122744791 A>T maps to NM_004506.3 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr6:122744791 A>T maps to NM_004506.3 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr7:21747447 T>C maps to NM_003777.3 D2233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr7:21747447 T>C maps to NM_003777.3 D2233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr7:82582564 A>C maps to NM_033026.5 S2568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr7:82582564 A>C maps to NM_033026.5 S2568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr7:100876195 C>A did not map to a codon.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr7:100876195 C>A did not map to a codon.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr7:121942224 A>G maps to NM_001024613.2 H418H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr7:121942224 A>G maps to NM_001024613.2 H418H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr7:138827002 T>C maps to NM_024926.2 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chr7:138827002 T>C maps to NM_024926.2 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chrX:18924611 C>T did not map to a codon.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chrX:18924611 C>T did not map to a codon.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chrX:54334450 A>G maps to NM_020922.4 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5367-01A-01D-1434-08 chrX:54334450 A>G maps to NM_020922.4 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:10659376 A>C maps to NM_004565.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:10659376 A>C maps to NM_004565.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:12785335 C>A maps to NM_001103170.1 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:12785335 C>A maps to NM_001103170.1 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:27874900 G>A maps to NM_001029882.2 F1242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:27874900 G>A maps to NM_001029882.2 F1242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:31347179 G>A maps to NM_014654.3 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:31347179 G>A maps to NM_014654.3 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:46655572 G>A maps to ENST00000371986 R580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:46655572 G>A maps to ENST00000371986 R580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:48703349 G>A did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:48703349 G>A did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:66827445 C>G maps to NM_001037341.1 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:66827445 C>G maps to NM_001037341.1 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:110765833 C>T maps to NM_004978.4 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:110765833 C>T maps to NM_004978.4 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:155735585 G>A maps to ENST00000368331 H1226H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:155735585 G>A maps to ENST00000368331 H1226H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:160053930 C>T maps to NM_004983.2 N37N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:160053930 C>T maps to NM_004983.2 N37N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:178414789 C>T maps to ENST00000263528 D522D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:178414789 C>T maps to ENST00000263528 D522D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:180885979 C>T maps to NM_020950.1 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:180885979 C>T maps to NM_020950.1 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:201333479 G>T maps to ENST00000421663 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:201333479 G>T maps to ENST00000421663 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr10:31137575 C>A maps to NM_182755.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr10:31137575 C>A maps to NM_182755.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr10:101715776 G>C maps to ENST00000342239 S485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr10:101715776 G>C maps to ENST00000342239 S485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr10:105172994 G>A maps to NM_014976.1 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr10:105172994 G>A maps to NM_014976.1 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:4112526 C>T maps to NM_003156.3 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:4112526 C>T maps to NM_003156.3 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:5373627 T>C maps to NM_001004750.1 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:5373627 T>C maps to NM_001004750.1 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:7064474 C>T maps to NM_176822.3 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:7064474 C>T maps to NM_176822.3 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:61539101 C>T maps to NM_001127392.1 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:61539101 C>T maps to NM_001127392.1 R291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:66276552 C>G maps to NM_005700.3 S682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:66276552 C>G maps to NM_005700.3 S682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:66411035 G>A maps to NM_001198845.1 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:66411035 G>A maps to NM_001198845.1 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:67262397 C>T maps to NM_004910.2 A887A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:67262397 C>T maps to NM_004910.2 A887A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:71249136 C>T maps to ENST00000422553 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:71249136 C>T maps to ENST00000422553 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:92715106 C>T maps to NM_005959.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:92715106 C>T maps to NM_005959.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:94113677 G>C maps to NM_016540.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:94113677 G>C maps to NM_016540.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:105924128 A>G maps to NM_198439.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:105924128 A>G maps to NM_198439.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:118352584 C>T maps to NM_001197104.1 R1264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr11:118352584 C>T maps to NM_001197104.1 R1264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:6886562 G>A maps to NM_002286.5 W397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:6886562 G>A maps to NM_002286.5 W397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:11214110 G>A maps to ENST00000422992 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:11214110 G>A maps to ENST00000422992 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:12274077 G>A maps to NM_002336.2 P1608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:12274077 G>A maps to NM_002336.2 P1608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:57005680 G>A maps to NM_013449.3 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:57005680 G>A maps to NM_013449.3 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:57348691 G>A maps to NM_003708.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:57348691 G>A maps to NM_003708.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:67699280 A>G maps to NM_018448.3 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:67699280 A>G maps to NM_018448.3 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:106464624 G>A maps to NM_014840.2 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:106464624 G>A maps to NM_014840.2 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:113714795 C>T maps to NM_001143819.1 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:113714795 C>T maps to NM_001143819.1 R411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:120150456 G>A maps to ENST00000392521 D1541D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr12:120150456 G>A maps to ENST00000392521 D1541D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr13:30104748 C>T maps to NM_003045.4 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr13:30104748 C>T maps to NM_003045.4 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr13:73636024 G>C maps to NM_001730.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr13:73636024 G>C maps to NM_001730.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr13:108861663 G>A maps to NM_001098268.1 N651N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr13:108861663 G>A maps to NM_001098268.1 N651N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr13:115089331 G>A maps to NM_032436.2 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr13:115089331 G>A maps to NM_032436.2 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr14:55453968 G>A maps to NM_007086.3 R555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr14:55453968 G>A maps to NM_007086.3 R555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr14:57092098 G>C did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr14:57092098 G>C did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr14:63174447 G>A maps to NM_139318.3 H915H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr14:63174447 G>A maps to NM_139318.3 H915H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr14:74411194 C>T maps to NM_152445.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr14:74411194 C>T maps to NM_152445.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr14:81610459 G>A maps to NM_000369.2 Q686Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr14:81610459 G>A maps to NM_000369.2 Q686Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr14:94187822 G>A maps to NM_178013.3 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr14:94187822 G>A maps to NM_178013.3 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr14:95670572 C>T maps to NM_024734.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr14:95670572 C>T maps to NM_024734.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:42104153 G>A did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:42104153 G>A did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:43940127 G>A maps to NM_172095.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:43940127 G>A maps to NM_172095.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:51221215 C>T maps to NM_007347.3 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:51221215 C>T maps to NM_007347.3 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:64017533 C>T maps to ENST00000261887 T1175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:64017533 C>T maps to ENST00000261887 T1175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:75702242 C>T maps to NM_001145357.1 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:75702242 C>T maps to NM_001145357.1 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:79327553 T>C did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:79327553 T>C did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:83679040 G>A maps to NM_144597.2 C62C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:83679040 G>A maps to NM_144597.2 C62C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:83698894 G>A maps to NM_025238.3 R350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:83698894 G>A maps to NM_025238.3 R350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:90321330 G>A maps to NM_001039958.1 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:90321330 G>A maps to NM_001039958.1 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:90611532 C>T maps to NM_198526.2 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:90611532 C>T maps to NM_198526.2 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:90784557 C>A maps to NM_001013657.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:90784557 C>A maps to NM_001013657.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:1652540 G>A maps to NM_014714.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:1652540 G>A maps to NM_014714.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:2283181 G>T maps to NM_004424.3 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:2283181 G>T maps to NM_004424.3 E352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:2880711 G>T maps to NM_145252.2 G60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:2880711 G>T maps to NM_145252.2 G60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:16103673 C>G maps to ENST00000399408 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:16103673 C>G maps to ENST00000399408 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:27539952 G>A maps to NM_001520.3 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:27539952 G>A maps to NM_001520.3 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:30974856 G>A maps to NM_014712.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:30974856 G>A maps to NM_014712.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:57597803 C>A maps to ENST00000349457 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:57597803 C>A maps to ENST00000349457 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:70367482 T>G maps to NM_007242.4 *480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:70367482 T>G maps to NM_007242.4 *480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:74951880 C>T maps to NM_030581.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:74951880 C>T maps to NM_030581.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:81253936 C>A maps to NM_052892.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:81253936 C>A maps to NM_052892.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:83999317 C>T maps to NM_013370.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:83999317 C>T maps to NM_013370.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:88778041 G>T did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:88778041 G>T did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:89254678 C>T maps to NM_004933.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr16:89254678 C>T maps to NM_004933.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr17:2867169 G>A maps to NM_015085.4 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr17:2867169 G>A maps to NM_015085.4 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr17:40722104 C>A maps to NM_170607.2 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr17:40722104 C>A maps to NM_170607.2 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr18:6983141 C>A maps to NM_005559.2 E1918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr18:6983141 C>A maps to NM_005559.2 E1918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr18:33269222 G>A maps to NM_020474.3 W316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr18:33269222 G>A maps to NM_020474.3 W316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr18:54448879 C>A maps to NM_015285.2 V1061V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr18:54448879 C>A maps to NM_015285.2 V1061V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr18:55274846 C>T maps to NM_004539.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr18:55274846 C>T maps to NM_004539.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr18:77170880 G>A maps to NM_172387.1 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr18:77170880 G>A maps to NM_172387.1 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:8181654 G>A maps to NM_032447.3 R1205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:8181654 G>A maps to NM_032447.3 R1205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:11030597 C>T maps to NM_199141.1 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:11030597 C>T maps to NM_199141.1 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:34912526 C>T maps to NM_032346.1 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:34912526 C>T maps to NM_032346.1 Q301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:36237738 C>T maps to NM_172341.1 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:36237738 C>T maps to NM_172341.1 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:43585207 G>A maps to ENST00000449000 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:43585207 G>A maps to ENST00000449000 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:44832113 A>G maps to ENST00000412927 G749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:44832113 A>G maps to ENST00000412927 G749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:50017241 G>C maps to NM_004107.4 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:50017241 G>C maps to NM_004107.4 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:51917031 C>T maps to NM_033130.4 R585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:51917031 C>T maps to NM_033130.4 R585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:52887775 C>T maps to NM_001145434.1 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:52887775 C>T maps to NM_001145434.1 Q315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:53344520 C>A maps to NM_001008801.1 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:53344520 C>A maps to NM_001008801.1 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:55014148 C>T maps to NM_002288.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:55014148 C>T maps to NM_002288.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:55086048 G>T maps to NM_001130917.1 G118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:55086048 G>T maps to NM_001130917.1 G118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:58601679 A>T maps to NM_001145542.1 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr19:58601679 A>T maps to NM_001145542.1 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:3504680 C>T maps to NM_018269.3 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:3504680 C>T maps to NM_018269.3 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:27684339 C>T maps to NM_015662.1 W746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:27684339 C>T maps to NM_015662.1 W746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:50149189 G>A maps to ENST00000404971 I1512I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:50149189 G>A maps to ENST00000404971 I1512I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:54856883 G>A maps to NM_003128.2 W871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:54856883 G>A maps to NM_003128.2 W871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:74725407 G>A maps to NM_001009812.1 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:74725407 G>A maps to NM_001009812.1 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:74756405 G>A maps to ENST00000258081 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:74756405 G>A maps to ENST00000258081 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:135745628 C>T maps to NM_025052.3 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:135745628 C>T maps to NM_025052.3 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:143676238 C>A maps to NM_003937.2 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:143676238 C>A maps to NM_003937.2 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:166032877 T>C maps to NM_006922.3 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:166032877 T>C maps to NM_006922.3 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:228881384 G>A maps to NM_001142644.1 N1395N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr2:228881384 G>A maps to NM_001142644.1 N1395N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr20:4843460 C>T maps to NM_203327.1 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr20:4843460 C>T maps to NM_203327.1 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr20:20493691 G>A maps to NM_020343.3 Q1441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr20:20493691 G>A maps to NM_020343.3 Q1441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr20:48744599 G>C maps to NM_199203.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr20:48744599 G>C maps to NM_199203.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr20:52188283 C>G maps to NM_006526.2 *1049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr20:52188283 C>G maps to NM_006526.2 *1049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr20:60508053 C>T maps to NM_001794.2 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr20:60508053 C>T maps to NM_001794.2 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr22:42154483 G>A maps to NM_152513.3 Q689Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr22:42154483 G>A maps to NM_152513.3 Q689Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr22:50647024 C>T maps to NM_031454.1 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr22:50647024 C>T maps to NM_031454.1 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr22:50654266 G>A maps to NM_031454.1 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr22:50654266 G>A maps to NM_031454.1 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:5249941 C>G maps to NM_014674.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:5249941 C>G maps to NM_014674.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:10146170 G>A maps to NM_001164839.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:10146170 G>A maps to NM_001164839.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:49455118 G>A maps to NM_000481.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:49455118 G>A maps to NM_000481.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:57613941 C>G maps to NM_152678.2 *609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:57613941 C>G maps to NM_152678.2 *609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:72799728 G>A maps to NM_018130.2 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:72799728 G>A maps to NM_018130.2 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:160968691 G>C maps to NM_015938.3 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:160968691 G>C maps to NM_015938.3 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:179096139 G>A maps to NM_033540.2 K447K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:179096139 G>A maps to NM_033540.2 K447K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:197579466 G>A maps to ENST00000425562 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr3:197579466 G>A maps to ENST00000425562 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr4:1729443 C>T maps to NM_006342.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr4:1729443 C>T maps to NM_006342.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr4:38016215 G>A maps to NM_015173.2 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr4:38016215 G>A maps to NM_015173.2 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr4:129043273 T>C maps to NM_018078.2 N485N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr4:129043273 T>C maps to NM_018078.2 N485N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr4:144459761 C>T maps to NM_003601.2 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr4:144459761 C>T maps to NM_003601.2 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr4:177650750 G>C maps to NM_005429.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr4:177650750 G>C maps to NM_005429.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr4:184930440 C>G maps to NM_020225.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr4:184930440 C>G maps to NM_020225.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr4:186425654 G>A maps to NM_014476.4 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr4:186425654 G>A maps to NM_014476.4 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:10405789 G>A did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:10405789 G>A did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:16694553 G>A maps to NM_012334.2 R1242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:16694553 G>A maps to NM_012334.2 R1242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:26906876 G>C maps to NM_016279.3 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:26906876 G>C maps to NM_016279.3 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:38427201 C>T maps to ENST00000354891 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:38427201 C>T maps to ENST00000354891 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:140744134 C>T maps to NM_018918.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:140744134 C>T maps to NM_018918.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:180666084 G>A maps to NM_006098.4 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr5:180666084 G>A maps to NM_006098.4 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr6:28962831 G>A maps to NM_001010877.2 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr6:28962831 G>A maps to NM_001010877.2 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr6:30122126 C>A maps to NM_006778.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr6:30122126 C>A maps to NM_006778.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr6:31238115 C>A maps to ENST00000383329 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr6:31238115 C>A maps to ENST00000383329 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr6:52318994 C>T maps to NM_018100.3 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr6:52318994 C>T maps to NM_018100.3 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr6:116574171 G>A maps to ENST00000368611 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr6:116574171 G>A maps to ENST00000368611 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr6:138615204 G>A maps to NM_020340.4 S1148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr6:138615204 G>A maps to NM_020340.4 S1148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr6:159462433 C>T maps to NM_054114.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr6:159462433 C>T maps to NM_054114.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:30094364 G>A maps to ENST00000440706 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:30094364 G>A maps to ENST00000440706 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:30485797 G>A maps to NM_006092.2 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:30485797 G>A maps to NM_006092.2 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:34724285 G>A maps to NM_207172.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:34724285 G>A maps to NM_207172.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:43906548 G>A maps to NM_032014.2 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:43906548 G>A maps to NM_032014.2 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:73455549 C>T maps to ENST00000358929 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:73455549 C>T maps to ENST00000358929 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:94996774 C>T maps to NM_000940.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:94996774 C>T maps to NM_000940.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:103835693 T>C maps to NM_002553.3 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:103835693 T>C maps to NM_002553.3 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:117375350 G>A maps to NM_033427.2 S1220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:117375350 G>A maps to NM_033427.2 S1220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:124386638 C>T maps to NM_005302.2 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:124386638 C>T maps to NM_005302.2 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:129910534 C>G maps to NM_001869.2 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:129910534 C>G maps to NM_001869.2 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:143701562 G>A maps to NM_001005281.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:143701562 G>A maps to NM_001005281.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:150945606 C>T maps to NM_001003801.1 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:150945606 C>T maps to NM_001003801.1 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:151884561 C>A did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr7:151884561 C>A did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr8:15480729 C>T maps to NM_006765.2 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr8:15480729 C>T maps to NM_006765.2 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr8:18729697 G>A maps to ENST00000440756 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr8:18729697 G>A maps to ENST00000440756 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr8:67578143 G>A maps to NM_025054.4 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr8:67578143 G>A maps to NM_025054.4 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr8:120569895 G>C maps to NM_006209.3 L871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr8:120569895 G>C maps to NM_006209.3 L871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr8:120772952 G>A maps to NM_003184.3 Q862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr8:120772952 G>A maps to NM_003184.3 Q862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr8:144548018 C>T did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr8:144548018 C>T did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr8:144947010 G>A maps to NM_031308.1 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr8:144947010 G>A maps to NM_031308.1 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr9:123758560 C>T maps to NM_001735.2 R936R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr9:123758560 C>T maps to NM_001735.2 R936R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr9:139396304 G>A maps to NM_017617.3 Q1845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr9:139396304 G>A maps to NM_017617.3 Q1845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chrX:2658838 G>A maps to NM_002414.3 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chrX:2658838 G>A maps to NM_002414.3 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chrX:37028000 C>T maps to NM_001013736.2 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chrX:37028000 C>T maps to NM_001013736.2 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chrX:77395060 G>T maps to NM_015975.4 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chrX:77395060 G>T maps to NM_015975.4 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chrX:99956325 C>T did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chrX:99956325 C>T did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chrX:107084401 G>A maps to NM_012216.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chrX:107084401 G>A maps to NM_012216.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chrX:108868221 G>A maps to NM_012282.2 R10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chrX:108868221 G>A maps to NM_012282.2 R10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chrX:127185699 G>T maps to NM_138289.3 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chrX:127185699 G>T maps to NM_138289.3 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chrX:129483263 C>A maps to ENST00000339231 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chrX:129483263 C>A maps to ENST00000339231 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chrX:139586055 C>T maps to NM_005634.2 Q390Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chrX:139586055 C>T maps to NM_005634.2 Q390Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chrX:149013597 C>T maps to NM_005364.4 C184C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chrX:149013597 C>T maps to NM_005364.4 C184C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr1:1325616 G>A maps to NM_030937.4 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr1:1325616 G>A maps to NM_030937.4 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr1:109446789 C>G maps to NM_013296.4 S369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr1:109446789 C>G maps to NM_013296.4 S369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr1:144882463 G>A maps to NM_014644.4 F1185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr1:144882463 G>A maps to NM_014644.4 F1185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr1:243362359 A>G did not map to a codon.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr1:243362359 A>G did not map to a codon.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr10:103921944 G>A maps to ENST00000405356 E683E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr10:103921944 G>A maps to ENST00000405356 E683E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr12:72425342 C>T maps to ENST00000389376 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr12:72425342 C>T maps to ENST00000389376 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr12:109201542 G>A maps to NM_018984.3 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr12:109201542 G>A maps to NM_018984.3 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr13:20041461 A>G maps to NM_199254.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr13:20041461 A>G maps to NM_199254.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr14:20781878 G>A maps to NM_182849.1 Q127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr14:20781878 G>A maps to NM_182849.1 Q127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr14:69257035 G>A maps to NM_004926.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr14:69257035 G>A maps to NM_004926.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr14:69701562 C>T maps to NM_001193363.1 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr14:69701562 C>T maps to NM_001193363.1 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr14:102516785 C>G maps to NM_001376.4 V4609V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr14:102516785 C>G maps to NM_001376.4 V4609V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr16:4164291 A>G maps to NM_001116.3 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr16:4164291 A>G maps to NM_001116.3 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr16:87960540 G>C maps to NM_001739.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr16:87960540 G>C maps to NM_001739.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr17:7578554 C>T did not map to a codon.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr17:7578554 C>T did not map to a codon.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr17:27068132 C>T maps to NM_178170.2 H590H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr17:27068132 C>T maps to NM_178170.2 H590H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr17:48243420 G>A maps to NM_000023.2 W7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr17:48243420 G>A maps to NM_000023.2 W7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr17:67094138 C>T maps to NM_080284.2 P1014P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr17:67094138 C>T maps to NM_080284.2 P1014P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr17:73568021 C>A maps to NM_001031803.1 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr17:73568021 C>A maps to NM_001031803.1 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr17:74639687 C>G maps to NM_018414.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr17:74639687 C>G maps to NM_018414.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr17:76354903 C>T maps to NM_003955.3 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr17:76354903 C>T maps to NM_003955.3 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr19:55107879 C>G maps to NM_006863.1 Y395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr19:55107879 C>G maps to NM_006863.1 Y395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr3:11300944 G>A maps to NM_001098211.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr3:11300944 G>A maps to NM_001098211.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr3:126180733 G>A maps to NM_025112.4 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr3:126180733 G>A maps to NM_025112.4 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr4:108935702 G>A maps to ENST00000351726 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr4:108935702 G>A maps to ENST00000351726 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr6:36989313 C>T maps to NM_173558.3 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr6:36989313 C>T maps to NM_173558.3 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr7:22190075 G>C maps to ENST00000344041 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr7:22190075 G>C maps to ENST00000344041 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr9:164037 C>G did not map to a codon.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr9:35389841 G>C did not map to a codon.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr9:35389841 G>C did not map to a codon.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr9:75775271 G>T maps to NM_000700.1 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chr9:75775271 G>T maps to NM_000700.1 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chrX:34961478 C>T maps to NM_152631.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chrX:34961478 C>T maps to NM_152631.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chrX:43601195 G>C did not map to a codon.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chrX:43601195 G>C did not map to a codon.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chrX:48931478 G>A maps to NM_007213.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chrX:48931478 G>A maps to NM_007213.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chrX:153284100 C>A maps to NM_001569.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chrX:153284100 C>A maps to NM_001569.3 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chrX:153608359 T>A maps to NM_000117.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5370-01A-01D-2012-08 chrX:153608359 T>A maps to NM_000117.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr1:33625293 G>A maps to NM_018207.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr1:33625293 G>A maps to NM_018207.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr1:44422612 G>A maps to NM_014652.3 W412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr1:44422612 G>A maps to NM_014652.3 W412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr1:152278059 G>C maps to NM_002016.1 S3101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr1:152278059 G>C maps to NM_002016.1 S3101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr1:198703457 T>C maps to ENST00000271610 G727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr1:198703457 T>C maps to ENST00000271610 G727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr10:70741336 G>A maps to NM_004728.2 Q694Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr10:70741336 G>A maps to NM_004728.2 Q694Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr11:7110533 C>T maps to NM_014469.4 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr11:7110533 C>T maps to NM_014469.4 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr11:35513608 G>A maps to NM_015430.2 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr11:35513608 G>A maps to NM_015430.2 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr11:66190250 A>T maps to NM_178864.3 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr11:66190250 A>T maps to NM_178864.3 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr11:92534194 A>G maps to ENST00000298047 T2672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr11:92534194 A>G maps to ENST00000298047 T2672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr11:94731016 C>T maps to NM_018039.2 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr11:94731016 C>T maps to NM_018039.2 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr11:117302400 C>T maps to NM_020693.2 R1801R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr11:117302400 C>T maps to NM_020693.2 R1801R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr12:6173439 G>A maps to NM_000552.3 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr12:6173439 G>A maps to NM_000552.3 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr12:132546771 C>T maps to ENST00000333577 R2704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr12:132546771 C>T maps to ENST00000333577 R2704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr13:27216529 G>A maps to NM_006646.5 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr13:27216529 G>A maps to NM_006646.5 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr13:42876730 C>T maps to NM_016248.2 F1283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr13:42876730 C>T maps to NM_016248.2 F1283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr14:61746908 G>A maps to NM_001017970.2 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr14:61746908 G>A maps to NM_001017970.2 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr16:532706 C>T maps to NM_014700.3 D362D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr16:532706 C>T maps to NM_014700.3 D362D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr16:58031443 C>T maps to NM_020807.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr16:58031443 C>T maps to NM_020807.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr17:10222178 C>T maps to NM_003802.2 E1222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr17:10222178 C>T maps to NM_003802.2 E1222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr17:56274610 C>T maps to NM_000502.4 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr17:56274610 C>T maps to NM_000502.4 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr18:50923745 G>A maps to NM_005215.3 S919S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr18:50923745 G>A maps to NM_005215.3 S919S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr19:49238476 C>T maps to NM_017805.2 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr19:49238476 C>T maps to NM_017805.2 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr19:58472908 G>A maps to NM_152474.4 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr19:58472908 G>A maps to NM_152474.4 Q128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr2:42557334 G>A maps to NM_019063.3 S978S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr2:42557334 G>A maps to NM_019063.3 S978S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr2:103324902 G>A maps to NM_003048.3 S798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr2:103324902 G>A maps to NM_003048.3 S798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr2:142238094 C>T maps to NM_018557.2 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr2:142238094 C>T maps to NM_018557.2 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr2:225670157 C>T maps to NM_014689.2 E1301E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr2:225670157 C>T maps to NM_014689.2 E1301E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr22:21133857 C>T maps to NM_000185.3 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr22:21133857 C>T maps to NM_000185.3 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr3:38357067 C>G maps to NM_004803.3 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr3:38357067 C>G maps to NM_004803.3 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr4:38691483 C>T maps to NM_016531.5 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr4:38691483 C>T maps to NM_016531.5 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr4:110433144 G>A maps to NM_006323.2 V603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr4:110433144 G>A maps to NM_006323.2 V603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr4:140810675 C>T maps to ENST00000509479 Q638Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr4:140810675 C>T maps to ENST00000509479 Q638Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr4:159791527 C>T maps to ENST00000379346 C975C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr4:159791527 C>T maps to ENST00000379346 C975C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:36037912 G>T maps to NM_174914.3 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:36037912 G>T maps to NM_174914.3 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:79031361 C>T maps to NM_153610.3 D2258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:79031361 C>T maps to NM_153610.3 D2258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:94764360 G>A maps to NM_152548.2 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:94764360 G>A maps to NM_152548.2 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:140222261 T>C maps to NM_018911.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:140222261 T>C maps to NM_018911.2 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:140229432 C>T maps to NM_031857.1 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:140229432 C>T maps to NM_031857.1 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:140579469 C>T maps to NM_018931.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:140579469 C>T maps to NM_018931.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:140743968 C>A maps to NM_018918.2 C24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:140743968 C>A maps to NM_018918.2 C24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:140794625 C>T maps to NM_018913.2 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:140794625 C>T maps to NM_018913.2 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:141336332 G>A maps to NM_016580.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:141336332 G>A maps to NM_016580.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:154305442 G>T maps to NM_015465.3 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr5:154305442 G>T maps to NM_015465.3 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr6:29454872 C>T maps to NM_052967.1 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr6:29454872 C>T maps to NM_052967.1 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr6:30865888 C>T maps to NM_013994.2 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr6:30865888 C>T maps to NM_013994.2 S758S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr6:33288741 G>A maps to NM_001350.4 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr6:33288741 G>A maps to NM_001350.4 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr6:166831721 G>A maps to ENST00000510118 D668D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr6:166831721 G>A maps to ENST00000510118 D668D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr7:57528991 C>G maps to NM_001159279.1 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr7:57528991 C>G maps to NM_001159279.1 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr7:102097842 A>T maps to NM_017621.3 *303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr7:102097842 A>T maps to NM_017621.3 *303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr7:143175525 C>A maps to NM_176883.2 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr7:143175525 C>A maps to NM_176883.2 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr8:134042150 C>T maps to NM_003235.4 G2374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr8:134042150 C>T maps to NM_003235.4 G2374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr8:134144070 G>A maps to NM_003235.4 A2626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr8:134144070 G>A maps to NM_003235.4 A2626A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr9:115598544 G>T maps to NM_001012994.1 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr9:115598544 G>T maps to NM_001012994.1 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr9:139090819 G>A maps to NM_014564.3 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chr9:139090819 G>A maps to NM_014564.3 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chrX:35821251 G>C maps to ENST00000422348 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chrX:35821251 G>C maps to ENST00000422348 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chrX:70830640 G>A maps to NM_052957.4 Q574Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chrX:70830640 G>A maps to NM_052957.4 Q574Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chrX:77254134 C>T maps to ENST00000355691 C565C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chrX:77254134 C>T maps to ENST00000355691 C565C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chrX:134305034 G>A maps to NM_001031705.2 R21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chrX:134305034 G>A maps to NM_001031705.2 R21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chrX:150844492 G>T maps to NM_173493.2 E734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5373-01A-01D-1434-08 chrX:150844492 G>T maps to NM_173493.2 E734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr1:21585218 G>C maps to NM_001397.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr1:21585218 G>C maps to NM_001397.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr1:100357190 C>T maps to ENST00000311030 F994F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr1:100357190 C>T maps to ENST00000311030 F994F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr1:155174871 C>T maps to NM_007112.3 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr1:155174871 C>T maps to NM_007112.3 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr1:211192355 G>A maps to NM_172362.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr1:211192355 G>A maps to NM_172362.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr1:237868593 A>G maps to NM_001035.2 K3177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr1:237868593 A>G maps to NM_001035.2 K3177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr10:24884721 T>C maps to NM_020824.3 K1212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr10:24884721 T>C maps to NM_020824.3 K1212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr10:50819670 C>T maps to NM_003055.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr10:50819670 C>T maps to NM_003055.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr10:100167371 C>T maps to NM_032709.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr10:100167371 C>T maps to NM_032709.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr10:116889157 A>G maps to NM_207303.2 Q230Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr10:116889157 A>G maps to NM_207303.2 Q230Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr10:118425269 G>T maps to ENST00000388884 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr10:118425269 G>T maps to ENST00000388884 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr10:124753990 G>A maps to NM_022466.5 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr10:124753990 G>A maps to NM_022466.5 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr11:20067213 C>A maps to ENST00000396087 R1323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr11:20067213 C>A maps to ENST00000396087 R1323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr11:94278549 G>A maps to NM_002033.3 Q417Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr11:94278549 G>A maps to NM_002033.3 Q417Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr12:48388218 C>T maps to NM_001844.4 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr12:48388218 C>T maps to NM_001844.4 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr12:112492279 G>A maps to NM_024953.3 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr12:112492279 G>A maps to NM_024953.3 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr12:113445709 C>T maps to NM_016817.2 T619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr12:113445709 C>T maps to NM_016817.2 T619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr12:131593381 G>A maps to NM_198827.3 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr12:131593381 G>A maps to NM_198827.3 S667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr13:111340149 C>T maps to NM_024537.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr13:111340149 C>T maps to NM_024537.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr15:35086907 C>A maps to NM_005159.4 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr15:35086907 C>A maps to NM_005159.4 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr15:45426425 C>T maps to NM_175940.1 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr15:45426425 C>T maps to NM_175940.1 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr15:82336382 G>A maps to NM_032246.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr15:82336382 G>A maps to NM_032246.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr16:67325247 G>A maps to NM_001100915.1 I843I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr16:67325247 G>A maps to NM_001100915.1 I843I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr16:75512868 C>T maps to NM_021615.4 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr16:75512868 C>T maps to NM_021615.4 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr16:84214951 C>T maps to NM_005679.2 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr16:84214951 C>T maps to NM_005679.2 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr17:5353645 G>T maps to ENST00000457531 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr17:5353645 G>T maps to ENST00000457531 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr17:17701460 G>A maps to ENST00000395776 S1733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr17:17701460 G>A maps to ENST00000395776 S1733S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr17:57775024 G>C maps to ENST00000409433 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr17:57775024 G>C maps to ENST00000409433 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr18:13885286 C>T maps to NM_000529.2 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr18:13885286 C>T maps to NM_000529.2 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr18:64239323 T>A maps to NM_021153.2 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr18:64239323 T>A maps to NM_021153.2 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr19:9067135 C>T maps to NM_024690.2 Q6770Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr19:9067135 C>T maps to NM_024690.2 Q6770Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr19:22817247 C>T did not map to a codon.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr19:22817247 C>T did not map to a codon.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr19:36205788 T>C maps to NM_014383.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr19:36205788 T>C maps to NM_014383.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr19:40580485 A>G maps to NM_001142577.1 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr19:40580485 A>G maps to NM_001142577.1 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr19:53958796 C>T maps to NM_001008401.3 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr19:53958796 C>T maps to NM_001008401.3 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr19:54445545 G>A maps to NM_031896.4 *276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr19:54445545 G>A maps to NM_031896.4 *276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr19:58059065 G>T maps to NM_001039654.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr19:58059065 G>T maps to NM_001039654.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr2:101188228 G>A maps to NM_024065.4 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr2:101188228 G>A maps to NM_024065.4 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr2:105708869 C>T maps to NM_182640.2 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr2:105708869 C>T maps to NM_182640.2 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr2:142888280 G>C maps to NM_018557.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr2:142888280 G>C maps to NM_018557.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr2:242196113 G>A maps to NM_005336.3 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr2:242196113 G>A maps to NM_005336.3 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr20:33444645 G>A maps to NM_178026.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr20:33444645 G>A maps to NM_178026.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr20:39744052 G>T maps to NM_003286.2 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr20:39744052 G>T maps to NM_003286.2 E561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr20:43379004 C>T maps to ENST00000372861 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr20:43379004 C>T maps to ENST00000372861 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr22:24718348 C>T maps to NM_015330.2 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr22:24718348 C>T maps to NM_015330.2 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr22:37892474 G>A maps to NM_014550.3 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr22:37892474 G>A maps to NM_014550.3 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr3:124418864 C>T maps to NM_001024660.3 R2661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr3:124418864 C>T maps to NM_001024660.3 R2661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr5:35705875 T>C maps to NM_024867.3 I877I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr5:35705875 T>C maps to NM_024867.3 I877I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr5:109152985 C>G maps to NM_002372.2 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr5:109152985 C>G maps to NM_002372.2 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr5:141336462 G>A maps to NM_016580.2 Y318Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr5:141336462 G>A maps to NM_016580.2 Y318Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:7229783 C>T maps to NM_001003699.3 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:7229783 C>T maps to NM_001003699.3 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:17764820 C>T maps to NM_022113.4 P1646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:17764820 C>T maps to NM_022113.4 P1646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:43006427 C>T maps to NM_001168370.1 A1565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:43006427 C>T maps to NM_001168370.1 A1565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:43590531 G>A maps to NM_019096.3 C435C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:43590531 G>A maps to NM_019096.3 C435C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:46657373 G>A maps to NM_001010870.2 W503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:46657373 G>A maps to NM_001010870.2 W503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:107955073 C>T maps to NM_018013.3 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:107955073 C>T maps to NM_018013.3 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:151766519 G>A maps to NM_017909.2 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:151766519 G>A maps to NM_017909.2 Q143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:155131213 C>G maps to NM_014892.3 S431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr6:155131213 C>G maps to NM_014892.3 S431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr7:6732044 G>C maps to ENST00000330442 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr7:6732044 G>C maps to ENST00000330442 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr7:20198240 G>A maps to NM_182762.3 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr7:20198240 G>A maps to NM_182762.3 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr7:112724578 A>G maps to NM_018970.6 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr7:112724578 A>G maps to NM_018970.6 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr7:127222111 G>A maps to NM_024523.5 R762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr7:127222111 G>A maps to NM_024523.5 R762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr8:140631106 G>A maps to NM_016601.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr8:140631106 G>A maps to NM_016601.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr9:95050072 C>T maps to ENST00000375660 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr9:95050072 C>T maps to ENST00000375660 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr9:95405068 C>T maps to NM_022755.5 Q176Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr9:95405068 C>T maps to NM_022755.5 Q176Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr9:113220759 G>A maps to ENST00000374463 I1189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr9:113220759 G>A maps to ENST00000374463 I1189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr9:114304894 C>T maps to NM_133464.2 F560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr9:114304894 C>T maps to NM_133464.2 F560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr9:115626606 G>A maps to NM_001012994.1 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr9:115626606 G>A maps to NM_001012994.1 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr9:129975311 G>A maps to NM_014636.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr9:129975311 G>A maps to NM_014636.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr9:136906944 C>T maps to NM_007371.3 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr9:136906944 C>T maps to NM_007371.3 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chrX:78010406 C>G maps to NM_005296.2 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chrX:78010406 C>G maps to NM_005296.2 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chrX:86068140 G>A maps to NM_053281.3 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chrX:86068140 G>A maps to NM_053281.3 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chrX:132730492 C>T maps to NM_001164617.1 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chrX:132730492 C>T maps to NM_001164617.1 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr1:29475098 G>T maps to NM_005626.4 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr1:29475098 G>T maps to NM_005626.4 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr1:183895365 G>A maps to NM_015149.3 T784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr1:183895365 G>A maps to NM_015149.3 T784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr1:186915839 G>T maps to NM_024420.2 G369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr1:186915839 G>T maps to NM_024420.2 G369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr1:248004730 G>A maps to NM_001001959.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr1:248004730 G>A maps to NM_001001959.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr10:121336172 C>T maps to NM_001033925.1 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr10:121336172 C>T maps to NM_001033925.1 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr11:58206943 G>C maps to NM_001004733.2 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr11:58206943 G>C maps to NM_001004733.2 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr11:62297925 G>T maps to NM_001620.1 P1321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr11:62297925 G>T maps to NM_001620.1 P1321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr11:65810580 C>T maps to NM_033036.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr11:65810580 C>T maps to NM_033036.2 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr11:112101362 G>C maps to NM_000317.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr11:112101362 G>C maps to NM_000317.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr11:130785039 C>G maps to NM_014758.2 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr11:130785039 C>G maps to NM_014758.2 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr12:11035683 C>A maps to NM_006250.2 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr12:11035683 C>A maps to NM_006250.2 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr12:32135422 A>T maps to NM_018169.3 K512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr12:32135422 A>T maps to NM_018169.3 K512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr12:62938683 C>T maps to ENST00000393630 Q826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr12:62938683 C>T maps to ENST00000393630 Q826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr12:66770983 G>A maps to ENST00000359742 C901C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr12:66770983 G>A maps to ENST00000359742 C901C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr12:132238981 C>T maps to NM_004592.2 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr12:132238981 C>T maps to NM_004592.2 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr13:32971099 C>A maps to NM_000059.3 P3189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr13:32971099 C>A maps to NM_000059.3 P3189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr13:38138654 C>T did not map to a codon.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr13:38138654 C>T did not map to a codon.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr14:21874022 C>A maps to NM_001170629.1 E970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr14:21874022 C>A maps to NM_001170629.1 E970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr14:96772062 G>C maps to NM_018036.5 T1532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr14:96772062 G>C maps to NM_018036.5 T1532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr14:102717261 C>G maps to NM_014226.1 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr14:102717261 C>G maps to NM_014226.1 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr14:105930440 G>T maps to NM_004689.3 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr14:105930440 G>T maps to NM_004689.3 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr15:43585694 G>T maps to NM_052955.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr15:43585694 G>T maps to NM_052955.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr15:90347555 G>A maps to NM_001150.2 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr15:90347555 G>A maps to NM_001150.2 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr16:15157136 T>G maps to NM_018427.3 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr16:15157136 T>G maps to NM_018427.3 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr16:51173270 G>A maps to ENST00000251020 S954S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr16:51173270 G>A maps to ENST00000251020 S954S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr16:65005484 G>A maps to NM_001797.2 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr16:65005484 G>A maps to NM_001797.2 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr16:76501309 T>A maps to NM_033401.3 C514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr16:76501309 T>A maps to NM_033401.3 C514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr17:34185927 C>T maps to NM_152781.2 Q301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr17:34185927 C>T maps to NM_152781.2 Q301Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr17:78319550 C>T maps to NM_020914.4 F2521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr17:78319550 C>T maps to NM_020914.4 F2521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr18:47421487 G>C maps to NM_001080467.2 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr18:47421487 G>C maps to NM_001080467.2 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr19:9069844 A>G maps to NM_024690.2 P5867P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr19:9069844 A>G maps to NM_024690.2 P5867P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr19:17476148 G>T maps to NM_031310.1 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr19:17476148 G>T maps to NM_031310.1 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr19:55718093 T>A maps to NM_002842.3 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr19:55718093 T>A maps to NM_002842.3 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr2:73826529 A>G maps to NM_015120.4 V3849V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr2:73826529 A>G maps to NM_015120.4 V3849V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr2:227920691 A>G maps to ENST00000396625 D895D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr2:227920691 A>G maps to ENST00000396625 D895D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr2:234296983 C>T maps to NM_152879.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr2:234296983 C>T maps to NM_152879.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr2:240061463 G>A maps to NM_006037.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr2:240061463 G>A maps to NM_006037.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr3:140251221 C>A maps to NM_022131.2 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr3:140251221 C>A maps to NM_022131.2 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr3:180321092 A>T maps to NM_133462.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr3:180321092 A>T maps to NM_133462.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr3:193166097 C>G maps to NM_032279.2 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr3:193166097 C>G maps to NM_032279.2 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr4:16760796 A>G maps to NM_001290.3 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr4:16760796 A>G maps to NM_001290.3 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr5:35641631 A>C maps to NM_024867.3 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr5:35641631 A>C maps to NM_024867.3 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr5:63509382 A>T did not map to a codon.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr5:63509382 A>T did not map to a codon.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr5:131714116 C>T maps to ENST00000435065 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr5:131714116 C>T maps to ENST00000435065 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr5:140216145 G>A maps to NM_018910.2 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr5:140216145 G>A maps to NM_018910.2 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr5:140579438 G>A maps to NM_018931.2 W31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr5:140579438 G>A maps to NM_018931.2 W31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr5:140735675 A>T maps to NM_018917.2 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr5:140735675 A>T maps to NM_018917.2 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr5:154179305 C>T maps to ENST00000377643 Y511Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr5:154179305 C>T maps to ENST00000377643 Y511Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr6:118790379 T>C maps to NM_001042475.2 K703K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr6:118790379 T>C maps to NM_001042475.2 K703K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr7:23240135 G>C maps to ENST00000413919 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr7:23240135 G>C maps to ENST00000413919 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr7:100681269 T>C maps to NM_001040105.1 P2191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr7:100681269 T>C maps to NM_001040105.1 P2191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr7:121701228 A>C maps to NM_002851.2 A2301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr7:121701228 A>C maps to NM_002851.2 A2301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr7:128492756 G>A maps to NM_001458.4 S1985S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr7:128492756 G>A maps to NM_001458.4 S1985S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr8:28906498 A>T maps to ENST00000444075 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr8:28906498 A>T maps to ENST00000444075 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr8:77896368 T>A maps to NM_001172087.1 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr8:77896368 T>A maps to NM_001172087.1 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr9:14146796 G>T maps to ENST00000397581 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chr9:14146796 G>T maps to ENST00000397581 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chrX:134994089 A>G maps to NM_018666.2 K833K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6010-01A-11D-1683-08 chrX:134994089 A>G maps to NM_018666.2 K833K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:981867 C>T maps to NM_198576.2 P1001P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:981867 C>T maps to NM_198576.2 P1001P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:27220787 C>T maps to NM_022078.2 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:27220787 C>T maps to NM_022078.2 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:41976646 C>G maps to NM_024503.3 L2232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:41976646 C>G maps to NM_024503.3 L2232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:75188945 G>A maps to NM_001889.3 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:75188945 G>A maps to NM_001889.3 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:92495680 C>T maps to NM_173567.4 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:92495680 C>T maps to NM_173567.4 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:119927520 C>T maps to ENST00000361035 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:119927520 C>T maps to ENST00000361035 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:152382204 C>G maps to NM_016190.2 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:152382204 C>G maps to NM_016190.2 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:154841648 T>C maps to NM_002249.4 Q264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:154841648 T>C maps to NM_002249.4 Q264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:179603611 G>T maps to ENST00000444136 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:179603611 G>T maps to ENST00000444136 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:202702866 G>A maps to ENST00000367264 Q1227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:202702866 G>A maps to ENST00000367264 Q1227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:216040364 C>G maps to ENST00000366943 V2943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:216040364 C>G maps to ENST00000366943 V2943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:243354557 C>G maps to NM_014812.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr1:243354557 C>G maps to NM_014812.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr10:75672796 G>A maps to NM_002658.3 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr10:75672796 G>A maps to NM_002658.3 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr10:102743389 G>C maps to NM_017893.2 V678V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr10:102743389 G>C maps to NM_017893.2 V678V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr10:105174041 T>C maps to NM_014976.1 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr10:105174041 T>C maps to NM_014976.1 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr10:126172786 C>T maps to NM_022126.3 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr10:126172786 C>T maps to NM_022126.3 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:1628958 G>A maps to ENST00000359229 C269C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:1628958 G>A maps to ENST00000359229 C269C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:1642735 G>A maps to NM_001012709.1 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:1642735 G>A maps to NM_001012709.1 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:30034072 G>C maps to NM_002233.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:30034072 G>C maps to NM_002233.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:59283059 G>C maps to NM_001004711.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:59283059 G>C maps to NM_001004711.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:59829988 C>T maps to NM_006138.4 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:59829988 C>T maps to NM_006138.4 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:62287083 C>T maps to NM_001620.1 P4935P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:62287083 C>T maps to NM_001620.1 P4935P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:65293809 C>T maps to NM_020680.3 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:65293809 C>T maps to NM_020680.3 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:117110555 C>T maps to NM_207343.2 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr11:117110555 C>T maps to NM_207343.2 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr12:31555437 G>T maps to NM_144973.3 T981T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr12:31555437 G>T maps to NM_144973.3 T981T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr12:49436572 G>T maps to NM_003482.3 T1911T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr12:49436572 G>T maps to NM_003482.3 T1911T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr12:124957521 C>T maps to NM_006312.4 Q189Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr12:124957521 C>T maps to NM_006312.4 Q189Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr12:130926552 G>A maps to NM_015347.4 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr12:130926552 G>A maps to NM_015347.4 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr13:33638295 G>A maps to NM_004795.3 S1004S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr13:33638295 G>A maps to NM_004795.3 S1004S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr13:79911234 A>G did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr13:79911234 A>G did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:51561182 G>A maps to ENST00000338969 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:51561182 G>A maps to ENST00000338969 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:63749900 C>T maps to NM_020663.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:63749900 C>T maps to NM_020663.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:68086771 G>A maps to NM_001172.3 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:68086771 G>A maps to NM_001172.3 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:75181622 C>G maps to NM_015962.4 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:75181622 C>G maps to NM_015962.4 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:75359640 C>T maps to NM_001933.4 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:75359640 C>T maps to NM_001933.4 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:76621244 C>G maps to NM_017926.2 S180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:76621244 C>G maps to NM_017926.2 S180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:81209425 C>T maps to NM_152446.3 E933E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:81209425 C>T maps to NM_152446.3 E933E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:99932039 T>A maps to NM_032233.2 K35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:99932039 T>A maps to NM_032233.2 K35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:105225820 G>A maps to NM_006427.3 *176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:105225820 G>A maps to NM_006427.3 *176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:105241316 G>A maps to NM_001014432.1 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr14:105241316 G>A maps to NM_001014432.1 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr15:31339442 C>T maps to NM_002420.4 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr15:31339442 C>T maps to NM_002420.4 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr15:40914963 G>A maps to NM_170589.3 Q860Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr15:40914963 G>A maps to NM_170589.3 Q860Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr15:72953675 C>T maps to NM_018652.4 N212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr15:72953675 C>T maps to NM_018652.4 N212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr15:75982532 G>A maps to NM_001897.4 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr15:75982532 G>A maps to NM_001897.4 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr15:79294084 G>A maps to NM_002891.4 Q848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr15:79294084 G>A maps to NM_002891.4 Q848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr16:17221546 G>A maps to NM_022166.3 D733D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr16:17221546 G>A maps to NM_022166.3 D733D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr16:61935157 G>A maps to NM_001796.2 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr16:61935157 G>A maps to NM_001796.2 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr16:71212845 C>T maps to NM_032821.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr16:71212845 C>T maps to NM_032821.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr16:74527005 C>G maps to NM_012201.5 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr16:74527005 C>G maps to NM_012201.5 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr17:6606427 G>A maps to NM_177550.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr17:6606427 G>A maps to NM_177550.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr17:56770069 G>A maps to NM_058216.1 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr17:56770069 G>A maps to NM_058216.1 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr18:9708422 C>G maps to NM_006868.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr18:9708422 C>G maps to NM_006868.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:3192540 C>T maps to NM_020170.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:3192540 C>T maps to NM_020170.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:14952227 C>G maps to NM_001005190.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:14952227 C>G maps to NM_001005190.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:21948579 C>T maps to NM_173531.3 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:21948579 C>T maps to NM_173531.3 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:39103306 G>A maps to NM_001042600.1 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:39103306 G>A maps to NM_001042600.1 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:44831902 G>A maps to ENST00000412927 Q820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:44831902 G>A maps to ENST00000412927 Q820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:49140148 G>A maps to NM_001352.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:49140148 G>A maps to NM_001352.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:50243128 G>A maps to NM_021733.1 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:50243128 G>A maps to NM_021733.1 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:52217096 G>A maps to NM_001523.2 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:52217096 G>A maps to NM_001523.2 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:54409998 G>A maps to NM_002739.3 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:54409998 G>A maps to NM_002739.3 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:24247129 G>T maps to ENST00000338315 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:24247129 G>T maps to ENST00000338315 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:32688440 C>T maps to NM_016252.3 Q1645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:32688440 C>T maps to NM_016252.3 Q1645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:106498396 C>T maps to NM_001004720.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:106498396 C>T maps to NM_001004720.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:128354095 C>T maps to ENST00000389524 L768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:128354095 C>T maps to ENST00000389524 L768L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:135738605 G>T maps to NM_025052.3 A1235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:135738605 G>T maps to NM_025052.3 A1235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:163144764 G>A maps to NM_022168.2 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:163144764 G>A maps to NM_022168.2 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:166901606 G>A maps to NM_001165963.1 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:166901606 G>A maps to NM_001165963.1 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:196729232 C>G maps to NM_018897.2 V2382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:196729232 C>G maps to NM_018897.2 V2382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:204732683 C>T maps to NM_005214.3 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:204732683 C>T maps to NM_005214.3 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:228159767 G>A maps to NM_000091.4 K1169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:228159767 G>A maps to NM_000091.4 K1169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:232143098 G>A maps to ENST00000359743 K493K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:232143098 G>A maps to ENST00000359743 K493K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:239990185 T>C maps to NM_006037.3 R951R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr2:239990185 T>C maps to NM_006037.3 R951R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr20:30584929 G>A maps to NM_001011718.1 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr20:30584929 G>A maps to NM_001011718.1 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr20:31607531 C>T maps to NM_025227.1 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr20:31607531 C>T maps to NM_025227.1 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr20:40980907 G>T maps to ENST00000373198 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr20:40980907 G>T maps to ENST00000373198 V526V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr22:24563211 G>A maps to NM_012295.3 Q1871Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr22:24563211 G>A maps to NM_012295.3 Q1871Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr22:32831729 G>A maps to NM_174932.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr22:32831729 G>A maps to NM_174932.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr22:40816945 G>T maps to NM_020831.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr22:40816945 G>T maps to NM_020831.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr3:9979743 C>T maps to NM_001077415.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr3:9979743 C>T maps to NM_001077415.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr3:15677116 C>T maps to NM_000060.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr3:15677116 C>T maps to NM_000060.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr3:55984541 G>A maps to ENST00000460849 Q772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr3:55984541 G>A maps to ENST00000460849 Q772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr3:154834750 G>A maps to NM_007289.2 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr3:154834750 G>A maps to NM_007289.2 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr3:156978934 G>C maps to NM_001167912.1 T830T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr3:156978934 G>C maps to NM_001167912.1 T830T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr3:182923662 C>T did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr3:182923662 C>T did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr4:62897306 C>T maps to ENST00000506720 F1190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr4:62897306 C>T maps to ENST00000506720 F1190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr4:90857797 G>A maps to NM_007351.2 S989S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr4:90857797 G>A maps to NM_007351.2 S989S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr4:164069512 G>C maps to NM_138386.2 S205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr4:164069512 G>C maps to NM_138386.2 S205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr4:169317110 G>C maps to NM_001012967.1 S1219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr4:169317110 G>C maps to NM_001012967.1 S1219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr4:170989839 T>G did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr4:170989839 T>G did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr5:9154807 C>G did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr5:9154807 C>G did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr5:16676205 G>A maps to NM_012334.2 R1534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr5:16676205 G>A maps to NM_012334.2 R1534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr5:38451421 C>G maps to ENST00000354891 S858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr5:38451421 C>G maps to ENST00000354891 S858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr5:127645020 C>G maps to NM_001999.3 V1757V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr5:127645020 C>G maps to NM_001999.3 V1757V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr5:156751059 C>T maps to ENST00000442283 F626F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr5:156751059 C>T maps to ENST00000442283 F626F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:12120395 C>G maps to NM_002114.2 S123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:12120395 C>G maps to NM_002114.2 S123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:24698241 T>C maps to NM_018473.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:24698241 T>C maps to NM_018473.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:31750117 G>C maps to NM_006295.2 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:31750117 G>C maps to NM_006295.2 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:38830054 G>A did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:38830054 G>A did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:43144379 C>T maps to NM_003131.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:43144379 C>T maps to NM_003131.2 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:109771219 C>T maps to NM_022765.3 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:109771219 C>T maps to NM_022765.3 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:116938127 G>C maps to NM_001010892.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:116938127 G>C maps to NM_001010892.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:132785160 G>A maps to NM_003569.2 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:132785160 G>A maps to NM_003569.2 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:132892294 T>C maps to NM_175067.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:132892294 T>C maps to NM_175067.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:139106385 G>A maps to NM_015439.2 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:139106385 G>A maps to NM_015439.2 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:139363854 G>C did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:139363854 G>C did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:152720762 T>A maps to NM_182961.2 K2409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:152720762 T>A maps to NM_182961.2 K2409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:160864769 C>T maps to ENST00000392145 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr6:160864769 C>T maps to ENST00000392145 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:33388765 C>T maps to NM_198428.2 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:33388765 C>T maps to NM_198428.2 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:47319948 G>C maps to NM_022748.11 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:47319948 G>C maps to NM_022748.11 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:50450283 G>A maps to NM_006060.3 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:50450283 G>A maps to NM_006060.3 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:70252203 C>G maps to NM_015570.2 S773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:70252203 C>G maps to NM_015570.2 S773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:91503288 C>G maps to NM_006980.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:91503288 C>G maps to NM_006980.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:93098028 G>A maps to NM_001164737.1 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:93098028 G>A maps to NM_001164737.1 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:99753353 C>T maps to NM_018275.3 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:99753353 C>T maps to NM_018275.3 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:103155674 G>A maps to ENST00000428762 V2692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr7:103155674 G>A maps to ENST00000428762 V2692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr8:67341836 G>A maps to NM_015169.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr8:67341836 G>A maps to NM_015169.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr8:110655122 A>G maps to NM_001099744.1 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr8:110655122 A>G maps to NM_001099744.1 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr8:119945203 C>T maps to NM_002546.3 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr8:119945203 C>T maps to NM_002546.3 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr8:145948231 C>T maps to NM_138367.1 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr8:145948231 C>T maps to NM_138367.1 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr8:146157371 G>A maps to NM_006958.2 C267C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr8:146157371 G>A maps to NM_006958.2 C267C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr9:6007496 G>A maps to NM_001017969.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr9:6007496 G>A maps to NM_001017969.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr9:92003800 G>A maps to NM_006378.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr9:92003800 G>A maps to NM_006378.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr9:92017920 C>T maps to NM_006378.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr9:92017920 C>T maps to NM_006378.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr9:93650071 G>A maps to NM_003177.5 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr9:93650071 G>A maps to NM_003177.5 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr9:103340679 C>T maps to NM_001018116.1 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr9:103340679 C>T maps to NM_001018116.1 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr9:111617355 G>A maps to NM_006686.3 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr9:111617355 G>A maps to NM_006686.3 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chrX:17768105 C>G maps to NM_001037540.1 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chrX:17768105 C>G maps to NM_001037540.1 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chrX:105179292 G>T maps to NM_198465.2 E1211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chrX:105179292 G>T maps to NM_198465.2 E1211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chrX:114540828 G>A maps to NM_016383.3 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chrX:114540828 G>A maps to NM_016383.3 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chrX:135427078 C>G maps to NM_153834.3 S405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chrX:135427078 C>G maps to NM_153834.3 S405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr1:9784116 C>T maps to ENST00000361110 H919H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr1:9784116 C>T maps to ENST00000361110 H919H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr1:161642855 C>G maps to NM_004001.4 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr1:161642855 C>G maps to NM_004001.4 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr1:197091046 G>A maps to NM_018136.4 Q1290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr1:197091046 G>A maps to NM_018136.4 Q1290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr10:15649677 G>A maps to NM_003638.1 R588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr10:15649677 G>A maps to NM_003638.1 R588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr10:16882890 G>A maps to NM_001081.3 I3273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr10:16882890 G>A maps to NM_001081.3 I3273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr10:44112549 G>A maps to NM_145312.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr10:44112549 G>A maps to NM_145312.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr10:103900409 C>T maps to NM_015062.3 S715S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr10:103900409 C>T maps to NM_015062.3 S715S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr11:55944827 G>T maps to NM_001005492.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr11:55944827 G>T maps to NM_001005492.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr12:333172 C>G maps to NM_016615.3 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr12:333172 C>G maps to NM_016615.3 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr12:60169149 C>G maps to NM_004731.3 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr12:60169149 C>G maps to NM_004731.3 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr13:99047719 G>A maps to NM_005766.2 Q468Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr13:99047719 G>A maps to NM_005766.2 Q468Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr14:64491049 C>T maps to NM_182914.2 L1905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr14:64491049 C>T maps to NM_182914.2 L1905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr14:100376628 T>G maps to NM_001008707.1 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr14:100376628 T>G maps to NM_001008707.1 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr15:40313218 C>T maps to NM_001013703.2 D1431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr15:40313218 C>T maps to NM_001013703.2 D1431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr16:16232271 G>A maps to ENST00000399408 T1458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr16:16232271 G>A maps to ENST00000399408 T1458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr16:71779056 G>A maps to ENST00000423132 I686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr16:71779056 G>A maps to ENST00000423132 I686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr19:4366920 A>G did not map to a codon.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr19:4366920 A>G did not map to a codon.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr19:22156074 G>T maps to NM_007153.3 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr19:22156074 G>T maps to NM_007153.3 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr19:36831736 G>A maps to NM_020917.2 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr19:36831736 G>A maps to NM_020917.2 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr19:47423336 G>T maps to NM_004491.4 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr19:47423336 G>T maps to NM_004491.4 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr2:152289597 A>G maps to NM_018151.4 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr2:152289597 A>G maps to NM_018151.4 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr2:233274347 C>T maps to NM_031313.2 D455D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr2:233274347 C>T maps to NM_031313.2 D455D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr20:45353863 G>T maps to NM_030777.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr20:45353863 G>T maps to NM_030777.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr22:46653800 G>A maps to NM_006071.1 L1807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr22:46653800 G>A maps to NM_006071.1 L1807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr22:46760505 G>A maps to NM_014246.1 R2894R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr22:46760505 G>A maps to NM_014246.1 R2894R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr3:108344784 G>T maps to NM_014648.3 G184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr3:108344784 G>T maps to NM_014648.3 G184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr3:121186389 G>A maps to ENST00000393672 R2451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr3:121186389 G>A maps to ENST00000393672 R2451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr3:157820502 C>T maps to NM_003030.4 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr3:157820502 C>T maps to NM_003030.4 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr4:24529591 G>A maps to NM_001358.2 D781D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr4:24529591 G>A maps to NM_001358.2 D781D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr4:187539226 G>T maps to ENST00000260147 S2841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr4:187539226 G>T maps to ENST00000260147 S2841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr5:19483428 G>A maps to NM_004934.3 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr5:19483428 G>A maps to NM_004934.3 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr5:24537630 G>A maps to NM_006727.3 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr5:24537630 G>A maps to NM_006727.3 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr6:88854381 C>T maps to NM_016083.4 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr6:88854381 C>T maps to NM_016083.4 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr6:151859253 C>G maps to ENST00000367290 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr6:151859253 C>G maps to ENST00000367290 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr7:128489487 G>A maps to NM_001458.4 P1685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr7:128489487 G>A maps to NM_001458.4 P1685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr8:104394751 C>G maps to NM_138455.2 S219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr8:104394751 C>G maps to NM_138455.2 S219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr9:21971095 C>A maps to NM_001195132.1 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr9:21971095 C>A maps to NM_001195132.1 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr9:79324741 C>T maps to NM_015225.2 W816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr9:79324741 C>T maps to NM_015225.2 W816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:53370494 C>T maps to ENST00000371522 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:53370494 C>T maps to ENST00000371522 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:64095638 A>T maps to NM_002633.2 K146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:64095638 A>T maps to NM_002633.2 K146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:158390344 G>A maps to NM_001004476.1 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:158390344 G>A maps to NM_001004476.1 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:178834725 C>T maps to NM_004673.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:178834725 C>T maps to NM_004673.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:185953401 C>T maps to NM_031935.2 N964N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:185953401 C>T maps to NM_031935.2 N964N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:201789045 C>T maps to ENST00000367296 Q1874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:201789045 C>T maps to ENST00000367296 Q1874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:248487681 G>A maps to NM_001004691.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:248487681 G>A maps to NM_001004691.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr10:38407108 C>T maps to NM_003421.2 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr10:38407108 C>T maps to NM_003421.2 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr10:78846272 G>A maps to NM_001161352.1 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr10:78846272 G>A maps to NM_001161352.1 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr10:104172142 G>A maps to NM_002779.3 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr10:104172142 G>A maps to NM_002779.3 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr10:104184419 G>A maps to NM_024040.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr10:104184419 G>A maps to NM_024040.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr10:124608955 C>G did not map to a codon.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr10:124608955 C>G did not map to a codon.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr11:613227 G>A maps to NM_004031.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr11:613227 G>A maps to NM_004031.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr11:46393101 C>T maps to NM_001105540.1 H424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr11:46393101 C>T maps to NM_001105540.1 H424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr11:118362544 C>T maps to NM_001197104.1 R1636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr11:118362544 C>T maps to NM_001197104.1 R1636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr12:21422496 C>T maps to NM_134431.3 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr12:21422496 C>T maps to NM_134431.3 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr12:53201524 G>A maps to NM_002272.2 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr12:53201524 G>A maps to NM_002272.2 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr12:96728557 A>G maps to NM_002595.4 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr12:96728557 A>G maps to NM_002595.4 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr14:23940185 G>A maps to NM_001042635.1 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr14:23940185 G>A maps to NM_001042635.1 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr14:92403315 C>T maps to ENST00000267620 Q215Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr14:92403315 C>T maps to ENST00000267620 Q215Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr16:72992973 G>A maps to NM_006885.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr16:72992973 G>A maps to NM_006885.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr17:3773160 G>C maps to ENST00000381771 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr17:3773160 G>C maps to ENST00000381771 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr17:77758351 C>T maps to NM_005189.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr17:77758351 C>T maps to NM_005189.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr19:5866612 C>T maps to NM_002034.2 *375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr19:5866612 C>T maps to NM_002034.2 *375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr19:14829869 C>T maps to NM_032433.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr19:14829869 C>T maps to NM_032433.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr19:23545291 G>A maps to NM_003430.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr19:23545291 G>A maps to NM_003430.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr19:37879379 G>A maps to NM_032453.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr19:37879379 G>A maps to NM_032453.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr19:56436022 C>T maps to NM_176810.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr19:56436022 C>T maps to NM_176810.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr2:20145564 G>A maps to NM_001006657.1 F620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr2:20145564 G>A maps to NM_001006657.1 F620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr2:130832650 G>A maps to NM_001099771.2 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr2:130832650 G>A maps to NM_001099771.2 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr2:163133417 C>A maps to NM_022168.2 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr2:163133417 C>A maps to NM_022168.2 E695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr2:238285727 C>T maps to NM_004369.3 A919A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr2:238285727 C>T maps to NM_004369.3 A919A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr20:2293572 C>T maps to NM_003245.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr20:2293572 C>T maps to NM_003245.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr20:10620403 C>T maps to NM_000214.2 T1133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr20:10620403 C>T maps to NM_000214.2 T1133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr20:17462558 G>A maps to NM_002594.2 W587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr20:17462558 G>A maps to NM_002594.2 W587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr20:34067177 G>A maps to NM_007186.3 A739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr20:34067177 G>A maps to NM_007186.3 A739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr20:43995542 C>T maps to NM_033542.3 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr20:43995542 C>T maps to NM_033542.3 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr20:62562254 C>T maps to NM_025219.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr20:62562254 C>T maps to NM_025219.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr22:31266527 C>T maps to NM_030758.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr22:31266527 C>T maps to NM_030758.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr22:37539601 C>T maps to ENST00000406505 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr22:37539601 C>T maps to ENST00000406505 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr22:39138355 C>A maps to ENST00000405018 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr22:39138355 C>A maps to ENST00000405018 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr3:129290405 G>A maps to NM_015103.2 F1094F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr3:129290405 G>A maps to NM_015103.2 F1094F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr3:131300470 C>T maps to ENST00000502818 K291K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr3:131300470 C>T maps to ENST00000502818 K291K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr3:184104640 G>A maps to NM_003741.2 T735T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr3:184104640 G>A maps to NM_003741.2 T735T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr3:195028030 C>A maps to NM_012287.5 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr3:195028030 C>A maps to NM_012287.5 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr5:64483989 T>C maps to NM_197941.2 T921T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr5:64483989 T>C maps to NM_197941.2 T921T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr5:82833069 C>T maps to NM_004385.4 L1416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr5:82833069 C>T maps to NM_004385.4 L1416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr5:137906698 G>A maps to NM_004134.6 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr5:137906698 G>A maps to NM_004134.6 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr5:140788503 C>T maps to NM_018926.2 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr5:140788503 C>T maps to NM_018926.2 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr5:169812328 G>A maps to NM_004137.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr5:169812328 G>A maps to NM_004137.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr5:178557034 G>A maps to NM_014244.4 S785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr5:178557034 G>A maps to NM_014244.4 S785S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr6:31749636 G>A maps to NM_006295.2 I778I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr6:31749636 G>A maps to NM_006295.2 I778I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr6:83847360 C>T maps to NM_015018.2 S1200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr6:83847360 C>T maps to NM_015018.2 S1200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr6:106973168 C>T maps to NM_001624.2 V1032V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr6:106973168 C>T maps to NM_001624.2 V1032V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr6:152510446 G>A maps to NM_182961.2 I7747I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr6:152510446 G>A maps to NM_182961.2 I7747I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr6:166944771 G>A maps to ENST00000510118 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr6:166944771 G>A maps to ENST00000510118 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr7:99305455 G>A maps to ENST00000292414 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr7:99305455 G>A maps to ENST00000292414 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr7:100463639 C>T maps to NM_020246.2 Q720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr7:100463639 C>T maps to NM_020246.2 Q720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr7:111400291 G>A maps to ENST00000428084 I1369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr7:111400291 G>A maps to ENST00000428084 I1369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr7:120629788 G>C maps to NM_024913.4 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr7:120629788 G>C maps to NM_024913.4 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr7:151900144 C>T maps to ENST00000355193 W1322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr7:151900144 C>T maps to ENST00000355193 W1322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr8:68992763 C>T maps to NM_024870.2 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr8:68992763 C>T maps to NM_024870.2 R577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr8:141900644 G>C maps to NM_005607.4 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr8:141900644 G>C maps to NM_005607.4 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr9:21971095 C>A maps to NM_001195132.1 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr9:21971095 C>A maps to NM_001195132.1 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr9:37512660 G>C maps to NM_012166.2 L918L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr9:37512660 G>C maps to NM_012166.2 L918L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr9:38016077 G>C maps to NM_003028.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr9:38016077 G>C maps to NM_003028.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr9:131019927 C>T maps to NM_004486.4 E863E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr9:131019927 C>T maps to NM_004486.4 E863E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr1:26527433 G>A maps to NM_198137.1 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr1:26527433 G>A maps to NM_198137.1 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr1:110199341 C>T maps to NM_000850.4 H15H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr1:110199341 C>T maps to NM_000850.4 H15H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr1:154492808 C>T maps to NM_001098475.1 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr1:154492808 C>T maps to NM_001098475.1 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr1:200635067 G>A maps to NM_001031725.4 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr1:200635067 G>A maps to NM_001031725.4 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr1:215901488 C>T maps to ENST00000366943 L3983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr1:215901488 C>T maps to ENST00000366943 L3983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr10:5804549 T>C maps to NM_017782.4 D2410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr10:5804549 T>C maps to NM_017782.4 D2410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr10:71166837 A>G did not map to a codon.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr10:71166837 A>G did not map to a codon.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr10:86014099 C>G maps to ENST00000358110 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr10:86014099 C>G maps to ENST00000358110 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr11:209867 G>A maps to NM_021932.4 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr11:209867 G>A maps to NM_021932.4 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr11:46771968 T>C maps to ENST00000415402 L1860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr11:46771968 T>C maps to ENST00000415402 L1860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr13:36700049 G>A maps to NM_004734.4 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr13:36700049 G>A maps to NM_004734.4 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr13:113773174 G>A maps to NM_000131.3 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr13:113773174 G>A maps to NM_000131.3 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr16:2052727 G>A maps to ENST00000431526 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr16:2052727 G>A maps to ENST00000431526 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr16:17221564 G>A maps to NM_022166.3 I727I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr16:17221564 G>A maps to NM_022166.3 I727I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr16:71674672 C>T maps to NM_001017967.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr16:71674672 C>T maps to NM_001017967.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr16:75513582 C>T maps to NM_021615.4 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr16:75513582 C>T maps to NM_021615.4 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr17:27042863 C>A maps to NM_001144943.1 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr17:27042863 C>A maps to NM_001144943.1 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr17:36483160 G>A maps to ENST00000398597 S2098S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr17:36483160 G>A maps to ENST00000398597 S2098S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr17:61621725 C>T maps to NM_030779.2 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr17:61621725 C>T maps to NM_030779.2 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr18:65179742 T>C maps to NM_032160.2 G711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr18:65179742 T>C maps to NM_032160.2 G711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr19:41622400 A>G maps to NM_000774.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr19:41622400 A>G maps to NM_000774.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr19:54653381 G>C maps to NM_014516.3 V498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr19:54653381 G>C maps to NM_014516.3 V498V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr2:130832563 G>A maps to NM_001099771.2 F827F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr2:130832563 G>A maps to NM_001099771.2 F827F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr2:178080539 T>C maps to NM_194247.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr2:178080539 T>C maps to NM_194247.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr2:179641975 G>A maps to NM_133378.4 R1572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr2:179641975 G>A maps to NM_133378.4 R1572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr2:201791526 G>T maps to NM_006190.4 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr2:201791526 G>T maps to NM_006190.4 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr20:7866451 G>A maps to NM_017545.2 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr20:7866451 G>A maps to NM_017545.2 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr22:17072822 G>A maps to NM_014406.4 C206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr22:17072822 G>A maps to NM_014406.4 C206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr3:25611300 C>T maps to NM_000965.3 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr3:25611300 C>T maps to NM_000965.3 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr3:44852483 G>A maps to NM_020242.2 E706E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr3:44852483 G>A maps to NM_020242.2 E706E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr4:72316994 T>C maps to NM_001098484.2 C433C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr4:72316994 T>C maps to NM_001098484.2 C433C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr4:96256762 T>C maps to NM_003728.3 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr4:96256762 T>C maps to NM_003728.3 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr5:140431658 C>T maps to NM_013340.2 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr5:140431658 C>T maps to NM_013340.2 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr6:24658076 G>A maps to NM_016614.2 Y160Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr6:24658076 G>A maps to NM_016614.2 Y160Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr6:33636357 C>G maps to ENST00000374316 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr6:33636357 C>G maps to ENST00000374316 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr6:42222640 C>T maps to NM_033502.2 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr6:42222640 C>T maps to NM_033502.2 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr6:52141937 T>A maps to ENST00000419835 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr6:52141937 T>A maps to ENST00000419835 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr6:70639471 C>T maps to NM_001858.4 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr6:70639471 C>T maps to NM_001858.4 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr9:88925619 C>T did not map to a codon.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr9:88925619 C>T did not map to a codon.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr9:97080989 A>T maps to NM_017561.1 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr9:97080989 A>T maps to NM_017561.1 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr9:104071491 G>T did not map to a codon.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr9:104071491 G>T did not map to a codon.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr9:125289434 G>A maps to ENST00000359439 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6016-01A-11D-1683-08 chr9:125289434 G>A maps to ENST00000359439 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6017-01A-11D-1683-08 chr2:183888620 T>C maps to NM_205842.1 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6017-01A-11D-1683-08 chr2:183888620 T>C maps to NM_205842.1 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6017-01A-11D-1683-08 chr6:29365003 C>G maps to NM_013936.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6017-01A-11D-1683-08 chr6:29365003 C>G maps to NM_013936.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr1:10477151 C>G maps to NM_002631.2 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr1:10477151 C>G maps to NM_002631.2 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr1:92495737 C>T maps to NM_173567.4 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr1:92495737 C>T maps to NM_173567.4 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr1:151735514 C>T maps to NM_031420.2 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr1:151735514 C>T maps to NM_031420.2 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr11:1098724 G>C maps to ENST00000441003 S2365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr11:1098724 G>C maps to ENST00000441003 S2365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr11:3380842 G>T maps to NM_001130520.1 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr11:3380842 G>T maps to NM_001130520.1 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr11:76969568 G>A maps to ENST00000376217 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr11:76969568 G>A maps to ENST00000376217 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr11:119029005 C>G maps to NM_001142505.1 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr11:119029005 C>G maps to NM_001142505.1 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr12:970336 A>G maps to NM_001184985.1 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr12:970336 A>G maps to NM_001184985.1 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr12:56718208 G>A maps to NM_001127460.2 D599D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr12:56718208 G>A maps to NM_001127460.2 D599D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr13:23906533 C>T maps to NM_014363.4 K3827K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr13:23906533 C>T maps to NM_014363.4 K3827K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr14:79933657 C>T maps to NM_004796.4 A746A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr14:79933657 C>T maps to NM_004796.4 A746A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr15:80845024 G>A maps to NM_014862.3 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr15:80845024 G>A maps to NM_014862.3 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr16:56875618 C>A maps to NM_014669.3 I741I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr16:56875618 C>A maps to NM_014669.3 I741I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr17:21319814 C>T maps to NM_021012.4 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr17:21319814 C>T maps to NM_021012.4 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr17:36091643 C>T maps to NM_000458.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr17:36091643 C>T maps to NM_000458.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr19:22939422 G>T maps to ENST00000397104 Y916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr19:22939422 G>T maps to ENST00000397104 Y916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr19:49143423 C>G maps to NM_001217.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr19:49143423 C>G maps to NM_001217.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr19:52394689 G>T maps to NM_023074.3 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr19:52394689 G>T maps to NM_023074.3 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr19:53669069 G>A maps to NM_024733.3 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr19:53669069 G>A maps to NM_024733.3 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr19:58213788 G>C maps to NM_001085384.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr19:58213788 G>C maps to NM_001085384.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr2:60688816 G>A maps to NM_022893.3 C410C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr2:60688816 G>A maps to NM_022893.3 C410C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr2:73993699 G>C maps to NM_003584.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr2:73993699 G>C maps to NM_003584.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr2:95846872 C>T maps to ENST00000453539 H113H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr2:95846872 C>T maps to ENST00000453539 H113H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr20:9561424 G>A maps to NM_177990.2 H119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr20:9561424 G>A maps to NM_177990.2 H119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr21:44474013 G>A maps to ENST00000398168 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr21:44474013 G>A maps to ENST00000398168 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr22:37770764 G>A maps to NM_052906.3 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr22:37770764 G>A maps to NM_052906.3 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr22:50967606 G>A maps to ENST00000395681 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr22:50967606 G>A maps to ENST00000395681 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr3:6903380 C>T maps to NM_181874.2 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr3:6903380 C>T maps to NM_181874.2 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr3:169557901 C>G maps to NM_024727.2 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr3:169557901 C>G maps to NM_024727.2 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr3:184074821 C>T maps to NM_004366.4 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr3:184074821 C>T maps to NM_004366.4 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr4:126239488 G>A maps to NM_024582.4 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr4:126239488 G>A maps to NM_024582.4 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr4:187630503 C>A maps to ENST00000260147 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr4:187630503 C>A maps to ENST00000260147 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr6:29080239 G>A maps to NM_001005216.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr6:29080239 G>A maps to NM_001005216.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr6:161508787 T>C maps to NM_005922.2 I875I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr6:161508787 T>C maps to NM_005922.2 I875I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr7:2317746 C>T maps to NM_013321.2 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr7:2317746 C>T maps to NM_013321.2 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr9:107558477 C>G maps to NM_005502.3 G1746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr9:107558477 C>G maps to NM_005502.3 G1746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chrX:47442864 G>A maps to NM_003254.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chrX:47442864 G>A maps to NM_003254.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chrX:64722773 G>A maps to NM_001010888.3 P732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chrX:64722773 G>A maps to NM_001010888.3 P732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chrX:122561965 C>T maps to NM_000828.4 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chrX:122561965 C>T maps to NM_000828.4 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chrX:124097536 A>T maps to NM_001163278.1 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chrX:124097536 A>T maps to NM_001163278.1 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chrX:151303807 C>T maps to NM_021048.3 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chrX:151303807 C>T maps to NM_021048.3 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr1:97272477 C>T maps to ENST00000370197 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr1:97272477 C>T maps to ENST00000370197 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr1:175046802 C>T maps to NM_022093.1 N83N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr1:175046802 C>T maps to NM_022093.1 N83N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr10:50724314 G>A maps to ENST00000515869 C750C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr10:50724314 G>A maps to ENST00000515869 C750C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr12:99065372 C>T maps to NM_181861.1 R557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr12:99065372 C>T maps to NM_181861.1 R557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr12:116445305 A>G maps to NM_015335.4 Y716Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr12:116445305 A>G maps to NM_015335.4 Y716Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr12:120634605 G>A maps to NM_053275.3 D308D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr12:120634605 G>A maps to NM_053275.3 D308D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr13:21562739 G>A maps to NM_014572.2 H393H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr13:21562739 G>A maps to NM_014572.2 H393H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr14:32586345 C>T maps to NM_001030055.1 Q1240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr14:32586345 C>T maps to NM_001030055.1 Q1240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr14:53345311 A>G maps to NM_001134999.1 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr14:53345311 A>G maps to NM_001134999.1 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr15:41819776 C>T maps to NM_015540.2 W485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr15:41819776 C>T maps to NM_015540.2 W485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr17:5290431 T>C did not map to a codon.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr17:5290431 T>C did not map to a codon.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr17:7350421 C>T maps to NM_000747.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr17:7350421 C>T maps to NM_000747.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr17:7574033 C>A did not map to a codon.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr17:7574033 C>A did not map to a codon.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr17:67094144 C>T maps to NM_080284.2 G1012G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr17:67094144 C>T maps to NM_080284.2 G1012G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr17:67111519 C>A maps to NM_080284.2 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr17:67111519 C>A maps to NM_080284.2 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr19:12297982 C>T maps to NM_003437.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr19:12297982 C>T maps to NM_003437.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr19:44222643 G>A did not map to a codon.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr19:44222643 G>A did not map to a codon.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr19:45262844 C>A maps to NM_005178.4 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr19:45262844 C>A maps to NM_005178.4 P446P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr19:55106220 G>A maps to NM_006863.1 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr19:55106220 G>A maps to NM_006863.1 E54E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr2:21255245 C>T maps to NM_000384.2 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr2:21255245 C>T maps to NM_000384.2 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr2:25463263 G>A maps to NM_175629.1 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr2:25463263 G>A maps to NM_175629.1 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr2:107459974 G>A maps to NM_001142351.1 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr2:107459974 G>A maps to NM_001142351.1 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr2:139316620 A>C maps to NM_001001664.2 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr2:139316620 A>C maps to NM_001001664.2 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr2:160031501 C>G maps to NM_033394.2 Y514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr2:160031501 C>G maps to NM_033394.2 Y514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr2:179598557 G>T maps to NM_133378.4 T3942T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr2:179598557 G>T maps to NM_133378.4 T3942T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr2:225365128 T>A maps to NM_003590.3 K521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr2:225365128 T>A maps to NM_003590.3 K521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr3:133372360 C>T maps to NM_007027.3 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr3:133372360 C>T maps to NM_007027.3 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr3:136714352 G>T maps to NM_144717.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr3:136714352 G>T maps to NM_144717.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr4:20852191 G>A maps to ENST00000382152 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr4:20852191 G>A maps to ENST00000382152 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr4:184938289 C>T maps to NM_020225.1 N878N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr4:184938289 C>T maps to NM_020225.1 N878N. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CN-6019-01A-11D-1683-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr6:33236965 G>A maps to NM_022553.4 R125*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CN-6019-01A-11D-1683-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr6:33236965 G>A maps to NM_022553.4 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr6:64416738 A>G maps to NM_015153.2 V1228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr6:64416738 A>G maps to NM_015153.2 V1228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr7:26225150 T>C maps to NM_004289.6 C611C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr7:26225150 T>C maps to NM_004289.6 C611C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr7:73008628 G>A maps to NM_032951.2 Y805Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr7:73008628 G>A maps to NM_032951.2 Y805Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr7:94058729 A>G maps to NM_000089.3 V1314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr7:94058729 A>G maps to NM_000089.3 V1314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr7:142749509 C>T maps to NM_001001667.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr7:142749509 C>T maps to NM_001001667.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr7:148288031 T>G maps to NM_145304.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr7:148288031 T>G maps to NM_145304.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr8:62212793 C>A maps to NM_173519.2 Y136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr8:62212793 C>A maps to NM_173519.2 Y136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr9:100862404 G>A maps to NM_033219.1 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chr9:100862404 G>A maps to NM_033219.1 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chrX:118221838 C>A maps to NM_020721.1 L1118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6019-01A-11D-1683-08 chrX:118221838 C>A maps to NM_020721.1 L1118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr1:66036307 G>T maps to NM_002303.5 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr1:66036307 G>T maps to NM_002303.5 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr1:70716155 A>G maps to NM_004768.3 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr1:70716155 A>G maps to NM_004768.3 E409E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr1:85331149 G>A maps to NM_012152.2 N218N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr1:85331149 G>A maps to NM_012152.2 N218N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr1:89657031 G>A maps to NM_052941.4 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr1:89657031 G>A maps to NM_052941.4 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr1:200550375 T>C maps to NM_014875.2 E1096E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr1:200550375 T>C maps to NM_014875.2 E1096E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr1:237947095 G>A maps to NM_001035.2 S4028S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr1:237947095 G>A maps to NM_001035.2 S4028S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr1:240072484 G>A maps to NM_000740.2 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr1:240072484 G>A maps to NM_000740.2 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr10:43678750 C>T maps to NM_018590.3 R464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr10:43678750 C>T maps to NM_018590.3 R464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr11:62458141 C>T maps to NM_001130702.1 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr11:62458141 C>T maps to NM_001130702.1 E392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr11:67262616 G>A maps to NM_004910.2 V854V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr11:67262616 G>A maps to NM_004910.2 V854V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr11:72292984 G>A maps to NM_002599.3 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr11:72292984 G>A maps to NM_002599.3 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr11:133712444 G>A maps to NM_174927.1 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr11:133712444 G>A maps to NM_174927.1 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr12:988981 C>T maps to NM_018979.3 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr12:988981 C>T maps to NM_018979.3 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr12:7653981 C>T maps to NM_004244.4 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr12:7653981 C>T maps to NM_004244.4 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr12:13716469 C>A maps to NM_000834.3 S1234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr12:13716469 C>A maps to NM_000834.3 S1234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr12:15035946 G>A maps to NM_001190839.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr12:15035946 G>A maps to NM_001190839.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr12:53012017 C>T maps to NM_175068.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr12:53012017 C>T maps to NM_175068.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr12:126128736 G>A maps to NM_052907.2 W513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr12:126128736 G>A maps to NM_052907.2 W513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr13:42295520 T>A maps to NM_015058.1 I983I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr13:42295520 T>A maps to NM_015058.1 I983I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr13:61985825 G>A maps to NM_022843.3 G802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr13:61985825 G>A maps to NM_022843.3 G802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr14:20692713 A>T maps to NM_001004480.1 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr14:20692713 A>T maps to NM_001004480.1 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr14:94417435 C>T maps to ENST00000434324 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr14:94417435 C>T maps to ENST00000434324 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr15:28386661 A>C maps to NM_004667.4 T3977T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr15:28386661 A>C maps to NM_004667.4 T3977T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr15:72668094 G>A maps to ENST00000457859 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr15:72668094 G>A maps to ENST00000457859 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr16:2166553 G>A maps to NM_001009944.2 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr16:2166553 G>A maps to NM_001009944.2 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr16:55530840 C>T maps to NM_004530.4 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr16:55530840 C>T maps to NM_004530.4 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr16:74537550 G>A maps to NM_012201.5 Q218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr16:74537550 G>A maps to NM_012201.5 Q218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr17:10418212 C>G did not map to a codon.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr17:10418212 C>G did not map to a codon.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr17:56233092 C>T maps to NM_012374.1 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr17:56233092 C>T maps to NM_012374.1 S193S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CN-6020-01A-11D-1683-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CN-6020-01A-11D-1683-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr19:5456158 G>A maps to NM_181710.3 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr19:5456158 G>A maps to NM_181710.3 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr19:12014458 G>A maps to ENST00000429654 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr19:12014458 G>A maps to ENST00000429654 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr19:17038879 G>A maps to ENST00000443236 F1160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr19:17038879 G>A maps to ENST00000443236 F1160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr19:57955190 G>A maps to NM_001023561.2 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr19:57955190 G>A maps to NM_001023561.2 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr2:55462058 G>A maps to NM_001177413.1 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr2:55462058 G>A maps to NM_001177413.1 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr2:61570971 A>G maps to NM_014709.3 I826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr2:61570971 A>G maps to NM_014709.3 I826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr2:170492732 G>T maps to NM_004792.2 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr2:170492732 G>T maps to NM_004792.2 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr2:197105284 A>G maps to NM_020760.1 L1218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr2:197105284 A>G maps to NM_020760.1 L1218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr2:203621982 G>A maps to NM_173511.3 Q384Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr2:203621982 G>A maps to NM_173511.3 Q384Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr2:234627537 C>G maps to NM_007120.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr2:234627537 C>G maps to NM_007120.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr20:4855260 T>A maps to NM_203327.1 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr20:4855260 T>A maps to NM_203327.1 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr21:11049618 T>A maps to NM_182482.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr21:11049618 T>A maps to NM_182482.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr22:19808241 G>A maps to NM_053004.2 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr22:19808241 G>A maps to NM_053004.2 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr3:9426230 A>G maps to NM_015453.2 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr3:9426230 A>G maps to NM_015453.2 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr3:49690315 G>A maps to NM_003458.3 L1109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr3:49690315 G>A maps to NM_003458.3 L1109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr5:24492956 G>C maps to NM_006727.3 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr5:24492956 G>C maps to NM_006727.3 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr5:37331894 C>G maps to NM_153485.1 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr5:37331894 C>G maps to NM_153485.1 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr5:131993988 G>T maps to NM_002188.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr5:131993988 G>T maps to NM_002188.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr5:140207690 G>A maps to NM_018909.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr5:140207690 G>A maps to NM_018909.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr5:154179272 C>T maps to ENST00000377643 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr5:154179272 C>T maps to ENST00000377643 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr6:42689519 G>A maps to NM_000322.4 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr6:42689519 G>A maps to NM_000322.4 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr6:117896461 T>C maps to NM_020399.3 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr6:117896461 T>C maps to NM_020399.3 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr7:72159742 G>A maps to NM_001145440.1 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr7:72159742 G>A maps to NM_001145440.1 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr8:10469744 C>T maps to NM_178857.5 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr8:10469744 C>T maps to NM_178857.5 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr8:38003512 G>A maps to NM_000349.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr8:38003512 G>A maps to NM_000349.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr8:42821702 G>C maps to NM_032410.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr8:42821702 G>C maps to NM_032410.3 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr8:48801648 C>A maps to NM_006904.6 L1401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr8:48801648 C>A maps to NM_006904.6 L1401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr8:48882490 A>C maps to NM_182746.1 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr8:48882490 A>C maps to NM_182746.1 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr8:121216035 G>A maps to NM_021110.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr8:121216035 G>A maps to NM_021110.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr8:145621931 C>A maps to NM_013291.2 E903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr8:145621931 C>A maps to NM_013291.2 E903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr9:116823280 G>A maps to NM_001633.3 Y317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr9:116823280 G>A maps to NM_001633.3 Y317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chrX:105011053 C>T maps to NM_017416.1 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chrX:105011053 C>T maps to NM_017416.1 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chrX:105450641 G>A maps to NM_001171020.1 W406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chrX:105450641 G>A maps to NM_001171020.1 W406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chrX:117775256 C>T maps to ENST00000276204 Q1417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chrX:117775256 C>T maps to ENST00000276204 Q1417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:12939817 C>T maps to ENST00000376192 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:12939817 C>T maps to ENST00000376192 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:20992740 G>A maps to NM_020816.2 S959S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:20992740 G>A maps to NM_020816.2 S959S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:37948749 G>A maps to NM_025079.2 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:37948749 G>A maps to NM_025079.2 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:57399014 G>A maps to NM_000066.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:57399014 G>A maps to NM_000066.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:75622594 T>C maps to NM_001001933.1 C276C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:75622594 T>C maps to NM_001001933.1 C276C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:75716975 G>A maps to NM_152697.4 N88N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:75716975 G>A maps to NM_152697.4 N88N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:152800094 A>G maps to NM_178348.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:152800094 A>G maps to NM_178348.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:241099908 G>T maps to ENST00000407727 Y108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr1:241099908 G>T maps to ENST00000407727 Y108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:8006136 C>T maps to NM_031923.2 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:8006136 C>T maps to NM_031923.2 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:32197131 C>A maps to NM_018287.5 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:32197131 C>A maps to NM_018287.5 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:48387901 G>T maps to NM_002900.2 L992L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:48387901 G>T maps to NM_002900.2 L992L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:50255050 T>A maps to NM_001031746.3 K272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:50255050 T>A maps to NM_001031746.3 K272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:50820090 G>A maps to NM_003055.2 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:50820090 G>A maps to NM_003055.2 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:95791540 T>C maps to ENST00000371380 N246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:95791540 T>C maps to ENST00000371380 N246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:112724465 C>G maps to NM_007373.3 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:112724465 C>G maps to NM_007373.3 S117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:131565233 G>A maps to NM_002412.3 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr10:131565233 G>A maps to NM_002412.3 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr11:64329823 C>T maps to NM_018484.2 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr11:64329823 C>T maps to NM_018484.2 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr11:123625127 G>A maps to NM_001005188.1 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr11:123625127 G>A maps to NM_001005188.1 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr12:5154797 C>T maps to NM_002234.2 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr12:5154797 C>T maps to NM_002234.2 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr12:18234235 G>A maps to NM_024730.2 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr12:18234235 G>A maps to NM_024730.2 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr12:21350087 C>A maps to NM_006446.4 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr12:21350087 C>A maps to NM_006446.4 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr12:53072486 C>T maps to NM_006121.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr12:53072486 C>T maps to NM_006121.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr12:53343349 G>A maps to NM_000224.2 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr12:53343349 G>A maps to NM_000224.2 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr12:55726161 G>T maps to NM_054104.1 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr12:55726161 G>T maps to NM_054104.1 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr12:112374540 G>A maps to NM_001193531.1 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr12:112374540 G>A maps to NM_001193531.1 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr13:99449734 A>G maps to ENST00000428223 A1989A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr13:99449734 A>G maps to ENST00000428223 A1989A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr13:113086836 T>A did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr13:113086836 T>A did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr15:35224629 C>T maps to NM_014691.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr15:35224629 C>T maps to NM_014691.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr15:38643247 C>T maps to NM_152594.2 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr15:38643247 C>T maps to NM_152594.2 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr15:43552358 C>G maps to NM_201631.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr15:43552358 C>G maps to NM_201631.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr15:91835754 A>G maps to NM_014848.4 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr15:91835754 A>G maps to NM_014848.4 P675P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr16:3293433 C>A maps to NM_000243.2 E685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr16:3293433 C>A maps to NM_000243.2 E685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr17:12618890 G>A maps to NM_001146312.1 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr17:12618890 G>A maps to NM_001146312.1 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr17:25932785 G>T maps to ENST00000268763 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr17:25932785 G>T maps to ENST00000268763 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr17:35297813 G>C did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr17:35297813 G>C did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr19:33110270 G>A maps to NM_032139.2 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr19:33110270 G>A maps to NM_032139.2 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr19:33517462 G>C maps to NM_033103.4 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr19:33517462 G>C maps to NM_033103.4 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr19:37733491 A>T maps to NM_152604.1 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr19:37733491 A>T maps to NM_152604.1 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr19:44791700 A>G maps to NM_004234.4 C629C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr19:44791700 A>G maps to NM_004234.4 C629C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr19:54327404 G>A maps to ENST00000391773 D8D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr19:54327404 G>A maps to ENST00000391773 D8D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr19:56953603 G>A maps to ENST00000342634 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr19:56953603 G>A maps to ENST00000342634 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr19:58187447 C>G did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr19:58187447 C>G did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr2:1440051 C>A maps to NM_000547.5 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr2:1440051 C>A maps to NM_000547.5 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr2:137852676 G>A maps to ENST00000272643 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr2:137852676 G>A maps to ENST00000272643 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr2:152321319 A>G maps to NM_018151.4 T1762T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr2:152321319 A>G maps to NM_018151.4 T1762T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr2:179478782 C>T maps to NM_133378.4 Q13879Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr2:179478782 C>T maps to NM_133378.4 Q13879Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr2:179482707 G>T maps to NM_133378.4 I13222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr2:179482707 G>T maps to NM_133378.4 I13222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr2:210574636 G>T did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr2:210574636 G>T did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr20:40068725 G>A maps to NM_032221.3 C1307C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr20:40068725 G>A maps to NM_032221.3 C1307C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr20:42195736 G>A maps to NM_016276.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr20:42195736 G>A maps to NM_016276.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr20:61594047 C>T maps to NM_022082.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr20:61594047 C>T maps to NM_022082.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr20:62737248 G>A maps to NM_005286.2 N312N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr20:62737248 G>A maps to NM_005286.2 N312N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr21:42647328 C>T maps to NM_012105.3 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr21:42647328 C>T maps to NM_012105.3 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr22:17280838 G>A maps to NM_175878.3 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr22:17280838 G>A maps to NM_175878.3 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr3:98073044 G>T maps to NM_001005517.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr3:98073044 G>T maps to NM_001005517.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr3:123451899 G>T maps to NM_053025.3 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr3:123451899 G>T maps to NM_053025.3 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr3:130327808 G>T did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr3:130327808 G>T did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr3:142742815 G>A did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr3:142742815 G>A did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr3:169639091 T>C maps to NM_182610.2 N59N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr3:169639091 T>C maps to NM_182610.2 N59N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr4:66230768 A>G maps to NM_004439.5 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr4:66230768 A>G maps to NM_004439.5 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr4:121631547 T>A maps to NM_018699.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr4:121631547 T>A maps to NM_018699.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:11346592 G>A maps to NM_001332.2 Q507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:11346592 G>A maps to NM_001332.2 Q507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:13721171 A>T maps to NM_001369.2 Y4072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:13721171 A>T maps to NM_001369.2 Y4072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:13845070 G>T maps to NM_001369.2 R1716R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:13845070 G>T maps to NM_001369.2 R1716R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:23510089 G>T maps to NM_020227.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:23510089 G>T maps to NM_020227.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:40853725 G>A maps to NM_032587.3 K764K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:40853725 G>A maps to NM_032587.3 K764K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:60067894 G>A maps to NM_024930.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:60067894 G>A maps to NM_024930.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:140554404 G>T maps to NM_018940.2 V663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:140554404 G>T maps to NM_018940.2 V663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:140719023 A>T maps to NM_018915.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr5:140719023 A>T maps to NM_018915.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr6:109802665 C>G maps to NM_014797.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr6:109802665 C>G maps to NM_014797.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr6:148869663 C>T maps to NM_015278.3 F1238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr6:148869663 C>T maps to NM_015278.3 F1238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr6:162683676 C>A maps to NM_004562.2 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr6:162683676 C>A maps to NM_004562.2 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr7:79082486 G>T maps to NM_012301.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr7:79082486 G>T maps to NM_012301.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr7:82585440 G>A maps to NM_033026.5 R1610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr7:82585440 G>A maps to NM_033026.5 R1610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr7:107638889 C>T maps to NM_002291.2 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr7:107638889 C>T maps to NM_002291.2 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr7:138946204 C>T maps to NM_173569.3 D371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr7:138946204 C>T maps to NM_173569.3 D371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr7:143417114 C>T maps to ENST00000441159 C321C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr7:143417114 C>T maps to ENST00000441159 C321C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr7:155596376 C>T maps to NM_000193.2 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr7:155596376 C>T maps to NM_000193.2 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr8:21973245 C>T maps to NM_005144.4 K1179K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr8:21973245 C>T maps to NM_005144.4 K1179K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr8:24168891 G>T maps to NM_014265.4 G109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr8:24168891 G>T maps to NM_014265.4 G109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr8:26721955 C>T maps to ENST00000356368 Q177Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr8:26721955 C>T maps to ENST00000356368 Q177Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr8:51571219 C>A maps to NM_018967.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr8:51571219 C>A maps to NM_018967.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr8:73848927 C>T maps to NM_004770.2 N446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr8:73848927 C>T maps to NM_004770.2 N446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr9:77411724 G>A maps to NM_017662.4 Q775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr9:77411724 G>A maps to NM_017662.4 Q775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr9:96209967 G>A maps to NM_198841.2 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr9:96209967 G>A maps to NM_198841.2 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr9:120470932 C>T maps to NM_138554.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr9:120470932 C>T maps to NM_138554.3 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr9:122004442 G>T maps to NM_014618.2 S154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr9:122004442 G>T maps to NM_014618.2 S154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr9:132658198 C>T maps to NM_015033.2 W588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr9:132658198 C>T maps to NM_015033.2 W588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chrX:69699024 A>T maps to ENST00000194900 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chrX:69699024 A>T maps to ENST00000194900 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chrX:80532533 G>T maps to NM_003022.2 G33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chrX:80532533 G>T maps to NM_003022.2 G33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chrX:92928012 C>T maps to NM_004538.5 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chrX:92928012 C>T maps to NM_004538.5 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chrX:107169921 C>A maps to NM_012216.3 Y609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chrX:107169921 C>A maps to NM_012216.3 Y609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chrX:107802346 A>C maps to ENST00000328300 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chrX:107802346 A>C maps to ENST00000328300 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chrX:118221771 G>T maps to NM_020721.1 R1141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chrX:118221771 G>T maps to NM_020721.1 R1141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr1:39317430 T>C did not map to a codon.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr1:39317430 T>C did not map to a codon.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:49438544 C>A maps to NM_003482.3 E1649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:49438544 C>A maps to NM_003482.3 E1649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:72666977 C>T maps to NM_013381.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:72666977 C>T maps to NM_013381.2 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:111758443 G>A maps to NM_015267.3 K877K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:111758443 G>A maps to NM_015267.3 K877K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:112578684 C>G maps to NM_006700.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:112578684 C>G maps to NM_006700.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:121605310 G>A maps to NM_002562.5 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:121605310 G>A maps to NM_002562.5 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:124268603 C>T maps to NM_207437.3 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:124268603 C>T maps to NM_207437.3 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:124285881 G>A maps to NM_207437.3 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:124285881 G>A maps to NM_207437.3 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:130827638 G>A maps to NM_004764.4 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr12:130827638 G>A maps to NM_004764.4 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr13:108861731 T>A maps to NM_001098268.1 K629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr13:108861731 T>A maps to NM_001098268.1 K629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr15:32921800 C>T maps to NM_014783.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr15:32921800 C>T maps to NM_014783.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr15:74738532 G>A maps to NM_201265.1 D347D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr15:74738532 G>A maps to NM_201265.1 D347D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr16:426288 C>T maps to NM_021259.2 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr16:426288 C>T maps to NM_021259.2 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr16:57994803 C>T maps to NM_001297.4 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr16:57994803 C>T maps to NM_001297.4 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr16:68011732 C>G did not map to a codon.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr16:68011732 C>G did not map to a codon.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr17:7577497 C>T did not map to a codon.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr17:7577497 C>T did not map to a codon.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr17:74287584 G>A maps to NM_032134.1 Q909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr17:74287584 G>A maps to NM_032134.1 Q909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr18:12697407 C>T did not map to a codon.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr18:12697407 C>T did not map to a codon.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr19:49631303 G>A maps to NM_003660.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr19:49631303 G>A maps to NM_003660.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr2:24929929 C>A maps to NM_003743.4 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr2:24929929 C>A maps to NM_003743.4 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr20:18022340 C>A maps to NM_021220.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr20:18022340 C>A maps to NM_021220.2 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr21:47635093 C>T maps to NM_002340.5 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr21:47635093 C>T maps to NM_002340.5 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr3:194063383 G>A maps to NM_001080513.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr3:194063383 G>A maps to NM_001080513.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr4:982692 G>A maps to NM_213613.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr4:982692 G>A maps to NM_213613.2 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr4:3432593 G>A maps to NM_198229.2 L1342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr4:3432593 G>A maps to NM_198229.2 L1342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr4:187088345 G>T maps to ENST00000356371 T726T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr4:187088345 G>T maps to ENST00000356371 T726T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr5:56212662 T>G maps to NM_153706.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr5:56212662 T>G maps to NM_153706.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr5:68680679 C>T maps to NM_133339.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr5:68680679 C>T maps to NM_133339.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr6:32154197 C>T maps to NM_002586.4 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr6:32154197 C>T maps to NM_002586.4 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr6:35213721 A>G maps to ENST00000394681 S883S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr6:35213721 A>G maps to ENST00000394681 S883S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr6:52303382 C>T maps to NM_018100.3 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr6:52303382 C>T maps to NM_018100.3 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr6:108843528 C>T maps to NM_145315.3 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr6:108843528 C>T maps to NM_145315.3 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr6:158483058 G>A maps to NM_003898.3 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr6:158483058 G>A maps to NM_003898.3 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr6:161160162 G>A maps to NM_000301.3 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr6:161160162 G>A maps to NM_000301.3 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr7:102098317 C>G maps to NM_017621.3 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr7:102098317 C>G maps to NM_017621.3 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr8:142441134 C>T maps to NM_032611.1 C171C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr8:142441134 C>T maps to NM_032611.1 C171C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr9:113148249 G>A maps to ENST00000374463 L3392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6022-01A-21D-1683-08 chr9:113148249 G>A maps to ENST00000374463 L3392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr1:982023 G>A maps to NM_198576.2 V1053V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr1:982023 G>A maps to NM_198576.2 V1053V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr1:35476585 G>A maps to NM_007167.3 Q372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr1:35476585 G>A maps to NM_007167.3 Q372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr1:59147829 G>A maps to NM_001085487.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr1:59147829 G>A maps to NM_001085487.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr10:27702585 G>A maps to NM_001034842.3 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr10:27702585 G>A maps to NM_001034842.3 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr10:95069803 G>A maps to NM_013451.3 F2040F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr10:95069803 G>A maps to NM_013451.3 F2040F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr10:112724420 C>G maps to NM_007373.3 S102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr10:112724420 C>G maps to NM_007373.3 S102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr12:49428363 C>T did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr12:49428363 C>T did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr12:49934899 C>T maps to NM_012284.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr12:49934899 C>T maps to NM_012284.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr16:2905797 C>T maps to NM_022119.3 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr16:2905797 C>T maps to NM_022119.3 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr16:80583379 G>C did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr16:80583379 G>C did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr18:19154818 T>A did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr18:19154818 T>A did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr19:39329126 C>T maps to ENST00000221419 E489E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr19:39329126 C>T maps to ENST00000221419 E489E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr19:41807559 C>T maps to NM_007040.3 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr19:41807559 C>T maps to NM_007040.3 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr2:18767630 C>T maps to ENST00000455492 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr2:18767630 C>T maps to ENST00000455492 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr2:26438044 C>T did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr2:26438044 C>T did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr2:29456499 A>T maps to NM_004304.3 R806R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr2:29456499 A>T maps to NM_004304.3 R806R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr2:73717131 A>G maps to NM_015120.4 E2681E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr2:73717131 A>G maps to NM_015120.4 E2681E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr2:99726006 T>C did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr2:99726006 T>C did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr20:35293460 T>G maps to ENST00000373803 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr20:35293460 T>G maps to ENST00000373803 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr20:35757570 C>G did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr20:35757570 C>G did not map to a codon.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr3:137843342 G>T maps to NM_016161.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr3:137843342 G>T maps to NM_016161.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr6:30547712 A>G maps to NM_001025091.1 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr6:30547712 A>G maps to NM_001025091.1 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr6:153347671 A>T maps to NM_012419.4 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr6:153347671 A>T maps to NM_012419.4 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr8:3087642 G>A maps to NM_033225.5 Q1422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr8:3087642 G>A maps to NM_033225.5 Q1422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr8:106814629 C>T maps to NM_012082.3 Q774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr8:106814629 C>T maps to NM_012082.3 Q774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr9:37948720 G>A maps to NM_003028.2 D419D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr9:37948720 G>A maps to NM_003028.2 D419D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr9:99150719 C>T maps to NM_153695.3 Q284Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr9:99150719 C>T maps to NM_153695.3 Q284Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr9:131088087 C>G maps to NM_016035.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chr9:131088087 C>G maps to NM_016035.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chrX:30268841 G>T maps to NM_177404.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chrX:30268841 G>T maps to NM_177404.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chrX:31497124 T>C maps to ENST00000357033 L2881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6023-01A-11D-1683-08 chrX:31497124 T>C maps to ENST00000357033 L2881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:43825056 C>T maps to NM_001255.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:43825056 C>T maps to NM_001255.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:46739821 C>T maps to NM_003579.3 V541V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:46739821 C>T maps to NM_003579.3 V541V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:75072414 T>A maps to NM_001002912.4 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:75072414 T>A maps to NM_001002912.4 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:87043753 C>T maps to ENST00000263723 N708N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:87043753 C>T maps to ENST00000263723 N708N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:98164953 G>A maps to NM_000110.3 Y211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:98164953 G>A maps to NM_000110.3 Y211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:152187702 T>C maps to NM_001009931.1 G2134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:152187702 T>C maps to NM_001009931.1 G2134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:243778439 A>C maps to NM_005465.3 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:243778439 A>C maps to NM_005465.3 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:247051785 A>G maps to ENST00000428671 D764D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr1:247051785 A>G maps to ENST00000428671 D764D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr10:14961767 C>A maps to NM_001033855.1 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr10:14961767 C>A maps to NM_001033855.1 L375L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CN-6024-01A-11D-1683-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-CN-6024-01A-11D-1683-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr10:126100542 T>C maps to NM_000274.3 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr10:126100542 T>C maps to NM_000274.3 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr11:5530479 T>G maps to NM_017481.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr11:5530479 T>G maps to NM_017481.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr11:34502383 T>A maps to NM_198381.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr11:34502383 T>A maps to NM_198381.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr11:40137316 G>T maps to NM_020929.1 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr11:40137316 G>T maps to NM_020929.1 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr11:66466926 G>T maps to NM_006946.2 G1242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr11:66466926 G>T maps to NM_006946.2 G1242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr11:92087365 A>G maps to ENST00000298047 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr11:92087365 A>G maps to ENST00000298047 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr11:111155056 G>A maps to NM_198498.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr11:111155056 G>A maps to NM_198498.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr11:122848578 G>A maps to NM_001098169.1 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr11:122848578 G>A maps to NM_001098169.1 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr12:27533230 G>A maps to NM_020183.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr12:27533230 G>A maps to NM_020183.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr12:50027755 C>T maps to NM_001031698.1 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr12:50027755 C>T maps to NM_001031698.1 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr12:124104213 G>A maps to NM_020936.1 K523K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr12:124104213 G>A maps to NM_020936.1 K523K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr13:48951100 T>C maps to NM_000321.2 D421D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr13:48951100 T>C maps to NM_000321.2 D421D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr13:79945212 G>A maps to ENST00000438737 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr13:79945212 G>A maps to ENST00000438737 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr14:24624490 C>G maps to NM_017999.4 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr14:24624490 C>G maps to NM_017999.4 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr14:31581698 T>C maps to NM_015382.2 L2067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr14:31581698 T>C maps to NM_015382.2 L2067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr14:55903568 A>G maps to NM_199047.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr14:55903568 A>G maps to NM_199047.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr14:94510930 G>A did not map to a codon.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr14:94510930 G>A did not map to a codon.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr15:81585275 A>T maps to NM_172217.3 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr15:81585275 A>T maps to NM_172217.3 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr16:836036 T>A maps to NM_058192.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr16:836036 T>A maps to NM_058192.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr16:72094647 C>T maps to NM_005143.3 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr16:72094647 C>T maps to NM_005143.3 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr17:8812416 C>A maps to NM_001142633.1 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr17:8812416 C>A maps to NM_001142633.1 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr17:10304047 G>T maps to NM_002472.2 R1132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr17:10304047 G>T maps to NM_002472.2 R1132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr17:10360800 C>A maps to NM_017533.2 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr17:10360800 C>A maps to NM_017533.2 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr17:15231308 C>A maps to NM_031898.2 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr17:15231308 C>A maps to NM_031898.2 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr17:73751848 A>C maps to NM_001005619.1 T1525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr17:73751848 A>C maps to NM_001005619.1 T1525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr19:1506028 C>T maps to NM_213604.2 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr19:1506028 C>T maps to NM_213604.2 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr19:9058237 C>A maps to NM_024690.2 T9736T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr19:9058237 C>A maps to NM_024690.2 T9736T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr19:17740102 T>A maps to ENST00000428389 A1321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr19:17740102 T>A maps to ENST00000428389 A1321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr19:37398927 T>C did not map to a codon.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr19:37398927 T>C did not map to a codon.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr19:54396286 G>A maps to NM_002739.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr19:54396286 G>A maps to NM_002739.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr19:57133987 A>T maps to NM_021216.4 K445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr19:57133987 A>T maps to NM_021216.4 K445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr2:27706460 C>T maps to NM_015662.1 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr2:27706460 C>T maps to NM_015662.1 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr2:29092864 C>T maps to NM_017910.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr2:29092864 C>T maps to NM_017910.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr2:103125362 G>T maps to NM_001011552.3 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr2:103125362 G>T maps to NM_001011552.3 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr2:106497976 C>T maps to NM_001004720.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr2:106497976 C>T maps to NM_001004720.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr2:161223851 G>T maps to NM_016836.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr2:161223851 G>T maps to NM_016836.3 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr20:9498786 T>C maps to NM_012261.3 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr20:9498786 T>C maps to NM_012261.3 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr20:22563618 G>C maps to NM_021784.4 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr20:22563618 G>C maps to NM_021784.4 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr20:31967482 C>T maps to ENST00000357886 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr20:31967482 C>T maps to ENST00000357886 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr20:31967497 C>G did not map to a codon.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr20:31967497 C>G did not map to a codon.
Multiple mappings detected for codon TCGA-CN-6024-01A-11D-1683-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr20:34021967 G>A maps to ENST00000374375 S4S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CN-6024-01A-11D-1683-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr20:34021967 G>A maps to ENST00000374375 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr21:46685543 A>G maps to NM_133635.4 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr21:46685543 A>G maps to NM_133635.4 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr22:40060148 C>T maps to NM_021096.3 G1217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr22:40060148 C>T maps to NM_021096.3 G1217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr3:97503852 T>A maps to NM_177976.1 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr3:97503852 T>A maps to NM_177976.1 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr3:126219566 A>T maps to NM_001165974.1 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr3:126219566 A>T maps to NM_001165974.1 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr3:160474320 T>C maps to NM_139245.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr3:160474320 T>C maps to NM_139245.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr3:164907250 G>T maps to NM_014926.2 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr3:164907250 G>T maps to NM_014926.2 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr3:171394567 T>G maps to NM_002662.3 A684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr3:171394567 T>G maps to NM_002662.3 A684A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr3:183547406 T>C maps to NM_018622.5 K373K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr3:183547406 T>C maps to NM_018622.5 K373K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr4:15835918 C>A maps to NM_001775.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr4:15835918 C>A maps to NM_001775.2 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr4:134084194 G>A maps to NM_032961.1 W954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr4:134084194 G>A maps to NM_032961.1 W954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr5:1432742 C>A maps to NM_001044.4 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr5:1432742 C>A maps to NM_001044.4 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr5:16877786 G>T maps to NM_012334.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr5:16877786 G>T maps to NM_012334.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr5:33937765 G>A maps to NM_016568.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr5:33937765 G>A maps to NM_016568.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr5:140215143 C>T maps to NM_018910.2 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr5:140215143 C>T maps to NM_018910.2 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr5:141336083 G>A maps to NM_016580.2 Q445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr5:141336083 G>A maps to NM_016580.2 Q445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr5:145506096 T>A maps to NM_020117.9 G964G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr5:145506096 T>A maps to NM_020117.9 G964G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr6:556004 T>C maps to NM_018303.4 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr6:556004 T>C maps to NM_018303.4 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr6:112513042 G>A maps to NM_001105206.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr6:112513042 G>A maps to NM_001105206.1 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr6:136977516 T>C maps to NM_005923.3 Q536Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr6:136977516 T>C maps to NM_005923.3 Q536Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr6:137814641 C>T maps to NM_175747.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr6:137814641 C>T maps to NM_175747.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr6:146127528 G>A maps to NM_032145.4 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr6:146127528 G>A maps to NM_032145.4 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr6:170592410 G>A maps to NM_005618.3 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr6:170592410 G>A maps to NM_005618.3 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr7:7628163 A>G maps to NM_019005.3 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr7:7628163 A>G maps to NM_019005.3 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr7:98931011 C>T maps to NM_006409.3 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr7:98931011 C>T maps to NM_006409.3 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr7:117351771 A>T maps to NM_033427.2 L1604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr7:117351771 A>T maps to NM_033427.2 L1604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr7:149474827 C>T maps to NM_198455.2 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr7:149474827 C>T maps to NM_198455.2 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr8:59410988 T>C maps to NM_000780.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr8:59410988 T>C maps to NM_000780.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr8:70744482 C>T maps to NM_030958.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr8:70744482 C>T maps to NM_030958.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr8:100789143 G>A maps to NM_017890.3 L2488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr8:100789143 G>A maps to NM_017890.3 L2488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr8:130765052 G>A maps to NM_031415.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr8:130765052 G>A maps to NM_031415.2 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr9:73399061 C>T maps to ENST00000419692 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr9:73399061 C>T maps to ENST00000419692 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr9:107267403 T>C maps to NM_001004485.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr9:107267403 T>C maps to NM_001004485.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr9:131515597 C>T maps to NM_006336.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chr9:131515597 C>T maps to NM_006336.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chrX:18660165 G>A maps to NM_000330.3 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chrX:18660165 G>A maps to NM_000330.3 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chrX:71887230 G>A maps to ENST00000373539 H237H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6024-01A-11D-1683-08 chrX:71887230 G>A maps to ENST00000373539 H237H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr1:42660588 T>G maps to NM_001198850.1 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr1:42660588 T>G maps to NM_001198850.1 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr1:155290742 C>T maps to NM_001039517.1 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr1:155290742 C>T maps to NM_001039517.1 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr1:161736176 C>A maps to NM_007348.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr1:161736176 C>A maps to NM_007348.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr1:173952660 C>A maps to NM_172071.2 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr1:173952660 C>A maps to NM_172071.2 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr1:207751507 C>A maps to NM_000651.4 A1632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr1:207751507 C>A maps to NM_000651.4 A1632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr1:214184943 C>G maps to NM_002763.3 Y638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr1:214184943 C>G maps to NM_002763.3 Y638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr10:8100733 C>A maps to NM_001002295.1 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr10:8100733 C>A maps to NM_001002295.1 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr10:17142172 A>C maps to NM_001081.3 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr10:17142172 A>C maps to NM_001081.3 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr10:52575976 A>T maps to NM_138932.2 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr10:52575976 A>T maps to NM_138932.2 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr10:70406097 T>C maps to NM_030625.2 H1204H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr10:70406097 T>C maps to NM_030625.2 H1204H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr10:91353634 C>A maps to NM_148977.1 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr10:91353634 C>A maps to NM_148977.1 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr11:22296275 A>T maps to NM_213599.2 R799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr11:22296275 A>T maps to NM_213599.2 R799R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr11:76253278 C>T maps to ENST00000393457 P860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr11:76253278 C>T maps to ENST00000393457 P860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr12:8083915 G>A maps to NM_006931.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr12:8083915 G>A maps to NM_006931.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr12:56740684 G>A maps to NM_005419.3 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr12:56740684 G>A maps to NM_005419.3 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr13:50293955 C>G did not map to a codon.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr13:50293955 C>G did not map to a codon.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr15:41549176 C>T maps to NM_007236.4 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr15:41549176 C>T maps to NM_007236.4 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr15:92459365 G>T maps to NM_013272.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr15:92459365 G>T maps to NM_013272.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr16:2339464 C>T maps to NM_001089.2 E890E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr16:2339464 C>T maps to NM_001089.2 E890E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr16:23646936 A>G maps to NM_024675.3 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr16:23646936 A>G maps to NM_024675.3 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr16:77327095 G>C maps to NM_199355.2 A1022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr16:77327095 G>C maps to NM_199355.2 A1022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr17:7386049 T>C maps to NM_001102614.1 D249D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr17:7386049 T>C maps to NM_001102614.1 D249D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr17:72278069 C>A maps to NM_023036.4 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr17:72278069 C>A maps to NM_023036.4 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr18:2738441 G>T maps to NM_015295.2 L1108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr18:2738441 G>T maps to NM_015295.2 L1108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr19:9008171 C>A did not map to a codon.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr19:9008171 C>A did not map to a codon.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr19:40023355 G>A maps to NM_152361.1 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr19:40023355 G>A maps to NM_152361.1 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr19:42569483 G>A maps to NM_002088.3 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr19:42569483 G>A maps to NM_002088.3 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr19:54758760 C>G maps to NM_001081442.1 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr19:54758760 C>G maps to NM_001081442.1 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr19:57335897 A>T maps to NM_006210.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr19:57335897 A>T maps to NM_006210.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr2:38301664 G>A maps to NM_000104.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr2:38301664 G>A maps to NM_000104.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr2:77745731 T>C maps to NM_001134745.1 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr2:77745731 T>C maps to NM_001134745.1 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr2:101607325 G>A maps to NM_002518.3 R701R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr2:101607325 G>A maps to NM_002518.3 R701R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr2:179532238 G>C maps to ENST00000392423 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr2:179532238 G>C maps to ENST00000392423 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr2:212251599 A>C maps to NM_005235.2 P1153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr2:212251599 A>C maps to NM_005235.2 P1153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr2:212543813 C>A maps to NM_005235.2 G529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr2:212543813 C>A maps to NM_005235.2 G529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr20:5753648 G>A maps to NM_152504.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr20:5753648 G>A maps to NM_152504.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr21:31803000 C>A maps to NM_181600.1 Y136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr21:31803000 C>A maps to NM_181600.1 Y136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr22:18650682 G>A maps to NM_017414.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr22:18650682 G>A maps to NM_017414.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr3:10050253 G>C did not map to a codon.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr3:10050253 G>C did not map to a codon.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr3:184002872 C>A maps to NM_014693.3 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr3:184002872 C>A maps to NM_014693.3 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr4:70156308 G>A did not map to a codon.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr4:70156308 G>A did not map to a codon.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr4:119952080 A>T maps to NM_133477.2 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr4:119952080 A>T maps to NM_133477.2 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr4:184931952 G>A maps to NM_020225.1 K654K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr4:184931952 G>A maps to NM_020225.1 K654K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr5:140563720 C>T maps to NM_020957.1 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr5:140563720 C>T maps to NM_020957.1 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr6:6266818 C>T maps to NM_000129.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr6:6266818 C>T maps to NM_000129.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr6:46849210 G>T maps to NM_015234.4 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr6:46849210 G>T maps to NM_015234.4 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr7:154664385 C>A maps to NM_130797.2 Y622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr7:154664385 C>A maps to NM_130797.2 Y622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr8:74858963 C>T maps to NM_005648.2 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr8:74858963 C>T maps to NM_005648.2 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr9:140137530 C>T maps to NM_006088.5 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chr9:140137530 C>T maps to NM_006088.5 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chrX:12736658 G>T maps to ENST00000429478 P1228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chrX:12736658 G>T maps to ENST00000429478 P1228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chrX:130409177 C>G maps to NM_001170961.1 G1094G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6988-01A-11D-1912-08 chrX:130409177 C>G maps to NM_001170961.1 G1094G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr1:2939014 G>A maps to NM_080431.4 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr1:2939014 G>A maps to NM_080431.4 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr1:28144384 G>A maps to ENST00000373939 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr1:28144384 G>A maps to ENST00000373939 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr1:57340683 C>A maps to NM_000562.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr1:57340683 C>A maps to NM_000562.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr10:18289627 C>T maps to NM_001145195.1 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr10:18289627 C>T maps to NM_001145195.1 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr11:4510852 G>A maps to NM_001005171.2 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr11:4510852 G>A maps to NM_001005171.2 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr11:47741493 G>A maps to NM_015308.2 Q984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr11:47741493 G>A maps to NM_015308.2 Q984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr11:123847522 G>T maps to NM_001004474.1 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr11:123847522 G>T maps to NM_001004474.1 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr12:26808651 G>A maps to NM_002223.2 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr12:26808651 G>A maps to NM_002223.2 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr12:51883735 G>A did not map to a codon.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr12:51883735 G>A did not map to a codon.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr12:122839066 G>A maps to ENST00000302528 R414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr12:122839066 G>A maps to ENST00000302528 R414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr13:111371618 C>T maps to NM_005537.3 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr13:111371618 C>T maps to NM_005537.3 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr14:60622826 C>T maps to NM_016029.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr14:60622826 C>T maps to NM_016029.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr15:75981391 G>A maps to NM_001897.4 R672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr15:75981391 G>A maps to NM_001897.4 R672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr18:2673309 C>G maps to NM_015295.2 S152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr18:2673309 C>G maps to NM_015295.2 S152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr18:31538214 C>T maps to NM_003787.4 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr18:31538214 C>T maps to NM_003787.4 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr19:56734094 G>A maps to NM_024303.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr19:56734094 G>A maps to NM_024303.1 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr2:43801883 C>T maps to ENST00000330266 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr2:43801883 C>T maps to ENST00000330266 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr2:109382139 C>T maps to NM_006267.4 S1715S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr2:109382139 C>T maps to NM_006267.4 S1715S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr2:179669321 C>T maps to NM_133378.4 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr2:179669321 C>T maps to NM_133378.4 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr2:206562313 C>T maps to NM_201266.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr2:206562313 C>T maps to NM_201266.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr2:225376089 C>T maps to NM_003590.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr2:225376089 C>T maps to NM_003590.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr22:31679216 T>A maps to NM_052880.4 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr22:31679216 T>A maps to NM_052880.4 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr3:46307686 A>T maps to NM_178328.1 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr3:46307686 A>T maps to NM_178328.1 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr3:164737434 C>T maps to NM_001041.3 L1126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr3:164737434 C>T maps to NM_001041.3 L1126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr3:179082964 C>T maps to NM_033540.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr3:179082964 C>T maps to NM_033540.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr4:120177468 A>G maps to NM_019050.2 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr4:120177468 A>G maps to NM_019050.2 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr4:187557926 G>A maps to ENST00000260147 R1262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr4:187557926 G>A maps to ENST00000260147 R1262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr5:140263130 C>T maps to NM_018904.2 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr5:140263130 C>T maps to NM_018904.2 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr6:44217785 G>A maps to NM_007355.2 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr6:44217785 G>A maps to NM_007355.2 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr6:47563618 G>A maps to NM_012120.2 Q377Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr6:47563618 G>A maps to NM_012120.2 Q377Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr6:50810852 G>A maps to ENST00000263046 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr6:50810852 G>A maps to ENST00000263046 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr7:72987686 G>A maps to NM_012453.2 H187H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr7:72987686 G>A maps to NM_012453.2 H187H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr8:22429317 C>T maps to NM_005775.4 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr8:22429317 C>T maps to NM_005775.4 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr8:110980373 C>T maps to NM_014379.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr8:110980373 C>T maps to NM_014379.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr9:94794748 A>G maps to NM_006415.2 *474Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr9:94794748 A>G maps to NM_006415.2 *474Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr9:112898858 C>T maps to NM_007203.4 H345H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr9:112898858 C>T maps to NM_007203.4 H345H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr9:139407979 G>T maps to NM_017617.3 C739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chr9:139407979 G>T maps to NM_017617.3 C739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chrX:101092615 C>T maps to ENST00000263032 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6989-01A-11D-1912-08 chrX:101092615 C>T maps to ENST00000263032 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:16890587 T>A maps to NM_017940.3 L1091L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:16890587 T>A maps to NM_017940.3 L1091L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:27684363 C>A maps to NM_004672.3 V973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:27684363 C>A maps to NM_004672.3 V973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:35333226 G>T maps to NM_001080418.1 I829I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:35333226 G>T maps to NM_001080418.1 I829I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:111490595 C>T maps to NM_018372.3 K765K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:111490595 C>T maps to NM_018372.3 K765K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:114193671 G>T maps to NM_001142782.1 E762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:114193671 G>T maps to NM_001142782.1 E762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:158656327 C>A did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:158656327 C>A did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:168200756 T>C maps to NM_199344.2 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:168200756 T>C maps to NM_199344.2 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:181702848 C>T maps to ENST00000357570 P1075P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:181702848 C>T maps to ENST00000357570 P1075P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:203708792 A>G maps to NM_001684.3 P1143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:203708792 A>G maps to NM_001684.3 P1143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:232577559 G>A maps to NM_020808.3 D1164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr1:232577559 G>A maps to NM_020808.3 D1164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr10:7239524 C>G maps to NM_001018039.1 V561V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr10:7239524 C>G maps to NM_001018039.1 V561V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr10:13222600 G>T maps to NM_182751.2 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr10:13222600 G>T maps to NM_182751.2 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr10:18807303 C>A maps to NM_201596.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr10:18807303 C>A maps to NM_201596.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr10:47915914 C>A maps to NM_018232.1 S441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr10:47915914 C>A maps to NM_018232.1 S441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr10:97050585 G>A maps to NM_020992.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr10:97050585 G>A maps to NM_020992.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr10:105162963 C>A maps to NM_014976.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr10:105162963 C>A maps to NM_014976.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr10:134598891 G>T maps to NM_177400.2 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr10:134598891 G>T maps to NM_177400.2 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:6661269 G>T maps to NM_003737.2 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:6661269 G>T maps to NM_003737.2 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:18158886 G>A maps to NM_054031.3 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:18158886 G>A maps to NM_054031.3 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:43428726 G>T maps to NM_018259.5 E601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:43428726 G>T maps to NM_018259.5 E601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:55340172 C>A maps to NM_001004701.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:55340172 C>A maps to NM_001004701.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:59189604 C>A maps to NM_001001954.1 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:59189604 C>A maps to NM_001001954.1 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:77413133 G>A maps to NM_016578.3 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:77413133 G>A maps to NM_016578.3 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:115049406 C>G maps to NM_014333.3 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:115049406 C>G maps to NM_014333.3 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:120989054 G>A maps to NM_005422.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr11:120989054 G>A maps to NM_005422.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr12:6438762 G>A maps to NM_001065.3 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr12:6438762 G>A maps to NM_001065.3 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr12:22063216 G>T maps to NM_005691.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr12:22063216 G>T maps to NM_005691.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr12:50035773 G>A maps to NM_001031698.1 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr12:50035773 G>A maps to NM_001031698.1 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr12:66814549 T>A maps to ENST00000359742 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr12:66814549 T>A maps to ENST00000359742 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr12:112512521 G>A maps to NM_024953.3 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr12:112512521 G>A maps to NM_024953.3 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr12:118590136 G>A maps to NM_016281.3 N810N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr12:118590136 G>A maps to NM_016281.3 N810N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr12:120650197 G>C maps to NM_001080855.1 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr12:120650197 G>C maps to NM_001080855.1 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr13:53624257 A>T maps to NM_006418.3 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr13:53624257 A>T maps to NM_006418.3 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr13:75936701 C>T maps to ENST00000431480 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr13:75936701 C>T maps to ENST00000431480 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr13:98642691 G>A maps to NM_002271.4 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr13:98642691 G>A maps to NM_002271.4 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr14:61519119 C>G maps to NM_153811.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr14:61519119 C>G maps to NM_153811.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr14:79933567 C>T maps to NM_004796.4 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr14:79933567 C>T maps to NM_004796.4 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr15:23931617 G>A maps to NM_002487.2 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr15:23931617 G>A maps to NM_002487.2 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr15:41688683 C>A did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr15:41688683 C>A did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr15:42168380 T>A maps to ENST00000320955 T1351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr15:42168380 T>A maps to ENST00000320955 T1351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr15:43910165 C>A maps to NM_153700.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr15:43910165 C>A maps to NM_153700.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr15:74032914 C>T maps to NM_001039614.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr15:74032914 C>T maps to NM_001039614.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr16:31308839 C>T maps to NM_001145808.1 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr16:31308839 C>T maps to NM_001145808.1 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr16:67574373 C>T maps to NM_001193523.1 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr16:67574373 C>T maps to NM_001193523.1 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr16:75146543 G>C maps to NM_153486.3 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr16:75146543 G>C maps to NM_153486.3 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr17:7290419 A>G maps to NM_003985.3 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr17:7290419 A>G maps to NM_003985.3 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr17:7918082 G>T did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr17:7918082 G>T did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr17:40705592 T>C maps to NM_000413.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr17:40705592 T>C maps to NM_000413.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:2216356 C>T maps to ENST00000221482 D667D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:2216356 C>T maps to ENST00000221482 D667D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:2993527 C>T maps to NM_001143986.1 H495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:2993527 C>T maps to NM_001143986.1 H495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:8555791 C>T maps to NM_032152.4 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:8555791 C>T maps to NM_032152.4 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:8987084 G>A maps to NM_024690.2 L13969L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:8987084 G>A maps to NM_024690.2 L13969L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:12767761 C>G did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:12767761 C>G did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:12848399 A>C maps to NM_004317.2 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:12848399 A>C maps to NM_004317.2 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:18368175 G>A maps to NM_001145304.1 A1306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:18368175 G>A maps to NM_001145304.1 A1306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:19166616 C>A maps to ENST00000392336 C391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:19166616 C>A maps to ENST00000392336 C391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:36832352 G>T maps to NM_020917.2 C125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:36832352 G>T maps to NM_020917.2 C125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:48342675 A>T maps to NM_000554.4 K118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:48342675 A>T maps to NM_000554.4 K118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:49477909 G>T maps to NM_002103.4 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:49477909 G>T maps to NM_002103.4 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:58718243 G>A maps to NM_133502.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr19:58718243 G>A maps to NM_133502.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr2:50573943 C>A maps to NM_138735.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr2:50573943 C>A maps to NM_138735.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr2:121740371 T>C maps to NM_005270.4 Y533Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr2:121740371 T>C maps to NM_005270.4 Y533Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr2:141201896 A>C did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr2:141201896 A>C did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr2:215275037 G>C maps to NM_024532.3 *632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr2:215275037 G>C maps to NM_024532.3 *632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr2:228973574 T>A maps to NM_001142644.1 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr2:228973574 T>A maps to NM_001142644.1 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr2:238242091 C>T did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr2:238242091 C>T did not map to a codon.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr20:46281791 T>C maps to NM_181659.2 S1413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr20:46281791 T>C maps to NM_181659.2 S1413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr20:48491308 C>A maps to ENST00000417961 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr20:48491308 C>A maps to ENST00000417961 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr21:34878304 C>T maps to NM_001136006.1 A853A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr21:34878304 C>T maps to NM_001136006.1 A853A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr22:32894168 G>A maps to NM_012179.3 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr22:32894168 G>A maps to NM_012179.3 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr22:50987659 C>T maps to NM_138433.3 Y355Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr22:50987659 C>T maps to NM_138433.3 Y355Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr3:45776774 C>T maps to NM_014016.3 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr3:45776774 C>T maps to NM_014016.3 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr3:126633571 C>G maps to ENST00000508789 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr3:126633571 C>G maps to ENST00000508789 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr3:127338054 G>A maps to NM_004526.2 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr3:127338054 G>A maps to NM_004526.2 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr3:154886356 C>A maps to NM_007289.2 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr3:154886356 C>A maps to NM_007289.2 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr3:164906544 G>T maps to NM_014926.2 R692R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr3:164906544 G>T maps to NM_014926.2 R692R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr4:41984018 G>T maps to NM_001029955.3 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr4:41984018 G>T maps to NM_001029955.3 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr4:100131355 G>T maps to NM_001102470.1 Y150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr4:100131355 G>T maps to NM_001102470.1 Y150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr4:147561488 C>A maps to NM_004575.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr4:147561488 C>A maps to NM_004575.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr4:159568072 C>A maps to ENST00000440678 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr4:159568072 C>A maps to ENST00000440678 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:10405686 C>T maps to NM_005885.2 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:10405686 C>T maps to NM_005885.2 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:43161389 A>T maps to ENST00000509156 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:43161389 A>T maps to ENST00000509156 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:45262556 G>C maps to NM_021072.2 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:45262556 G>C maps to NM_021072.2 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:45695880 C>A maps to NM_021072.2 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:45695880 C>A maps to NM_021072.2 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:71756258 G>A maps to NM_152625.1 H355H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:71756258 G>A maps to NM_152625.1 H355H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:140553885 G>C maps to NM_018940.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:140553885 G>C maps to NM_018940.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:140751527 G>T maps to NM_018924.2 E523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:140751527 G>T maps to NM_018924.2 E523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:169509799 C>T maps to NM_004946.2 L1811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:169509799 C>T maps to NM_004946.2 L1811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:179296769 T>A maps to NM_198868.2 P930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:179296769 T>A maps to NM_198868.2 P930P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:180218666 C>A maps to NM_001114617.1 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:180218666 C>A maps to NM_001114617.1 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:180429672 G>A maps to NM_197975.2 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr5:180429672 G>A maps to NM_197975.2 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:10529179 G>A maps to NM_145649.4 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:10529179 G>A maps to NM_145649.4 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:30672318 G>C maps to NM_014641.2 V1547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:30672318 G>C maps to NM_014641.2 V1547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:39869181 G>T maps to ENST00000398904 R972R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:39869181 G>T maps to ENST00000398904 R972R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:44197180 G>A maps to ENST00000313248 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:44197180 G>A maps to ENST00000313248 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:47775956 C>A maps to ENST00000489301 S275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:47775956 C>A maps to ENST00000489301 S275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:48036040 G>A maps to NM_001013732.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:48036040 G>A maps to NM_001013732.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:74063747 G>A maps to NM_001025290.2 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:74063747 G>A maps to NM_001025290.2 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:137814986 G>A maps to NM_175747.2 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:137814986 G>A maps to NM_175747.2 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:151055104 C>T maps to NM_001029884.1 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr6:151055104 C>T maps to NM_001029884.1 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr7:35674849 C>T maps to NM_022373.4 W279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr7:35674849 C>T maps to NM_022373.4 W279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr7:114284742 G>C maps to NM_148898.3 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr7:114284742 G>C maps to NM_148898.3 S356S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CN-6992-01A-11D-1912-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CN-6992-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:30889785 C>G maps to NM_013357.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:30889785 C>G maps to NM_013357.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:42171929 C>T maps to NM_001556.2 Y261Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:42171929 C>T maps to NM_001556.2 Y261Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:53084517 C>T maps to NM_014682.2 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:53084517 C>T maps to NM_014682.2 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:61769308 G>A maps to NM_017780.2 S2490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:61769308 G>A maps to NM_017780.2 S2490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:134225120 C>A maps to NM_003882.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:134225120 C>A maps to NM_003882.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:139691865 A>T maps to NM_152888.1 C1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:139691865 A>T maps to NM_152888.1 C1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:141561466 G>A maps to NM_012154.3 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:141561466 G>A maps to NM_012154.3 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:144996153 G>C maps to NM_201380.2 S2749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:144996153 G>C maps to NM_201380.2 S2749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:145626156 C>T maps to NM_013291.2 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr8:145626156 C>T maps to NM_013291.2 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr9:32784252 T>A maps to NM_212558.2 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr9:32784252 T>A maps to NM_212558.2 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr9:72006632 G>C maps to NM_001127608.1 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr9:72006632 G>C maps to NM_001127608.1 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr9:90264867 G>A maps to NM_004938.2 W487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chr9:90264867 G>A maps to NM_004938.2 W487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chrX:31089992 C>G maps to NM_031894.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chrX:31089992 C>G maps to NM_031894.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chrX:102979898 G>T maps to NM_001024452.2 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chrX:102979898 G>T maps to NM_001024452.2 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chrX:109695338 C>T maps to NM_020769.2 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chrX:109695338 C>T maps to NM_020769.2 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chrX:135429437 C>T maps to NM_153834.3 F1191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chrX:135429437 C>T maps to NM_153834.3 F1191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chrX:147743455 C>T maps to NM_002025.3 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chrX:147743455 C>T maps to NM_002025.3 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chrX:154261753 C>T maps to NM_023934.3 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6992-01A-11D-1912-08 chrX:154261753 C>T maps to NM_023934.3 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr1:54607035 C>T maps to NM_201546.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr1:54607035 C>T maps to NM_201546.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr10:102748350 C>T maps to NM_021830.4 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr10:102748350 C>T maps to NM_021830.4 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr10:107012615 C>A maps to NM_014978.1 P1063P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr10:107012615 C>A maps to NM_014978.1 P1063P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr11:6631165 G>A did not map to a codon.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr11:6631165 G>A did not map to a codon.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr13:32729800 T>A did not map to a codon.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr13:32729800 T>A did not map to a codon.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr16:723124 C>T maps to NM_138769.1 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr16:723124 C>T maps to NM_138769.1 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr16:2134998 C>G maps to NM_000548.3 S1514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr16:2134998 C>G maps to NM_000548.3 S1514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr16:3614103 G>A maps to ENST00000448023 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr16:3614103 G>A maps to ENST00000448023 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr17:26089929 G>A maps to NM_000625.4 S898S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr17:26089929 G>A maps to NM_000625.4 S898S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr17:30302526 T>C maps to NM_015355.2 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr17:30302526 T>C maps to NM_015355.2 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr17:74073205 C>A maps to NM_003857.2 C286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr17:74073205 C>A maps to NM_003857.2 C286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr17:76046390 G>A maps to NM_001142640.1 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr17:76046390 G>A maps to NM_001142640.1 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr18:55103823 G>C maps to NM_004852.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr18:55103823 G>C maps to NM_004852.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr19:1993165 G>C maps to NM_017797.3 Y179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr19:1993165 G>C maps to NM_017797.3 Y179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr19:20728195 G>A maps to NM_001159293.1 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr19:20728195 G>A maps to NM_001159293.1 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr19:49224213 G>A maps to NM_017805.2 I911I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr19:49224213 G>A maps to NM_017805.2 I911I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr19:52794351 G>A maps to NM_001010851.2 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr19:52794351 G>A maps to NM_001010851.2 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr19:55670430 C>G maps to ENST00000301249 *609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr19:55670430 C>G maps to ENST00000301249 *609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr2:197990617 G>A maps to NM_001195144.1 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr2:197990617 G>A maps to NM_001195144.1 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr2:197990623 G>A maps to NM_001195144.1 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr2:197990623 G>A maps to NM_001195144.1 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr2:197990662 G>A maps to NM_001195144.1 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr2:197990662 G>A maps to NM_001195144.1 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr2:197990751 G>A maps to NM_001195144.1 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr2:197990751 G>A maps to NM_001195144.1 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr20:34091851 G>A maps to NM_007186.3 L1885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr20:34091851 G>A maps to NM_007186.3 L1885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr21:39671653 G>A maps to NM_170736.1 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr21:39671653 G>A maps to NM_170736.1 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr22:41623844 G>A maps to NM_031488.4 K620K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr22:41623844 G>A maps to NM_031488.4 K620K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr3:42660539 G>C maps to NM_005385.3 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr3:42660539 G>C maps to NM_005385.3 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr3:136573475 G>C maps to NM_025246.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr3:136573475 G>C maps to NM_025246.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr3:167512408 G>T maps to NM_005025.4 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr3:167512408 G>T maps to NM_005025.4 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr4:39233471 G>T maps to NM_025132.3 E680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr4:39233471 G>T maps to NM_025132.3 E680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr4:153896098 G>C maps to NM_033393.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr4:153896098 G>C maps to NM_033393.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr5:453740 C>T maps to ENST00000315013 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr5:453740 C>T maps to ENST00000315013 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr5:50685738 C>G maps to NM_002202.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr5:50685738 C>G maps to NM_002202.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr5:140167278 C>T maps to NM_018900.2 N468N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr5:140167278 C>T maps to NM_018900.2 N468N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr5:141244695 C>G maps to NM_032420.2 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr5:141244695 C>G maps to NM_032420.2 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr6:37429755 C>T maps to NM_015050.2 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr6:37429755 C>T maps to NM_015050.2 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr6:41065109 C>T maps to NM_002505.4 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr6:41065109 C>T maps to NM_002505.4 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr6:142688949 A>G maps to NM_198569.2 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr6:142688949 A>G maps to NM_198569.2 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr7:30951586 G>T maps to NM_198098.2 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr7:30951586 G>T maps to NM_198098.2 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr7:47915767 G>A maps to NM_138295.3 H1237H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr7:47915767 G>A maps to NM_138295.3 H1237H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr7:76891593 T>C maps to NM_020879.2 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr7:76891593 T>C maps to NM_020879.2 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr8:23702399 A>C maps to NM_003155.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr8:23702399 A>C maps to NM_003155.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr8:41791309 C>T maps to NM_006766.3 A1476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr8:41791309 C>T maps to NM_006766.3 A1476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr9:17388166 C>G maps to NM_017738.2 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr9:17388166 C>G maps to NM_017738.2 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr9:35661157 C>T maps to NM_174923.2 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr9:35661157 C>T maps to NM_174923.2 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr9:104319875 C>T maps to NM_019592.5 Q794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr9:104319875 C>T maps to NM_019592.5 Q794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr9:110073971 T>C maps to NM_002874.3 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr9:110073971 T>C maps to NM_002874.3 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr9:112899837 C>A maps to NM_007203.4 R672R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6994-01A-11D-1912-08 chr9:112899837 C>A maps to NM_007203.4 R672R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr1:28384546 T>C did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr1:28384546 T>C did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr1:91180102 C>T maps to NM_020063.1 W279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr1:91180102 C>T maps to NM_020063.1 W279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr1:158047872 G>T maps to ENST00000368173 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr1:158047872 G>T maps to ENST00000368173 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr1:179363132 T>A maps to NM_144696.4 L320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr1:179363132 T>A maps to NM_144696.4 L320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr10:95791985 C>T maps to ENST00000371380 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr10:95791985 C>T maps to ENST00000371380 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr10:102584501 G>A maps to NM_003987.3 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr10:102584501 G>A maps to NM_003987.3 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr10:134464008 G>T maps to NM_005539.3 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr10:134464008 G>T maps to NM_005539.3 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr10:135346243 A>T maps to NM_000773.3 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr10:135346243 A>T maps to NM_000773.3 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr11:45672188 G>A maps to NM_003654.4 H95H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr11:45672188 G>A maps to NM_003654.4 H95H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr11:58979530 G>A maps to NM_001039396.1 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr11:58979530 G>A maps to NM_001039396.1 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr11:68506203 G>C maps to NM_004923.3 S294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr11:68506203 G>C maps to NM_004923.3 S294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr11:123676664 C>A maps to NM_001005325.1 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr11:123676664 C>A maps to NM_001005325.1 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr12:7556293 G>A maps to ENST00000416109 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr12:7556293 G>A maps to ENST00000416109 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr12:11420651 C>T maps to NM_006249.4 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr12:11420651 C>T maps to NM_006249.4 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr12:21030850 T>A maps to NM_019844.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr12:21030850 T>A maps to NM_019844.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr12:29597151 A>G maps to NM_183378.2 P981P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr12:29597151 A>G maps to NM_183378.2 P981P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr12:57918501 G>A did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr12:57918501 G>A did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr13:28931820 T>A maps to NM_002019.4 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr13:28931820 T>A maps to NM_002019.4 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr13:88329466 G>A maps to NM_015567.1 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr13:88329466 G>A maps to NM_015567.1 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr14:24045141 G>A maps to NM_032452.2 N301N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr14:24045141 G>A maps to NM_032452.2 N301N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr14:53020233 C>A maps to NM_001099652.1 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr14:53020233 C>A maps to NM_001099652.1 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr14:93118017 C>G maps to NM_024832.3 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr14:93118017 C>G maps to NM_024832.3 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr15:32921914 G>T maps to NM_014783.3 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr15:32921914 G>T maps to NM_014783.3 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr15:41804996 C>T maps to NM_002344.5 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr15:41804996 C>T maps to NM_002344.5 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr15:44890997 C>A maps to NM_025137.3 G1241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr15:44890997 C>A maps to NM_025137.3 G1241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr15:65667660 C>A maps to NM_004884.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr15:65667660 C>A maps to NM_004884.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr15:84506851 C>A maps to NM_207517.2 C204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr15:84506851 C>A maps to NM_207517.2 C204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr16:2273688 G>A maps to NM_004424.3 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr16:2273688 G>A maps to NM_004424.3 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr16:5143490 G>T maps to NM_201400.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr16:5143490 G>T maps to NM_201400.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr16:30490650 G>A did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr16:30490650 G>A did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr16:57067575 G>A maps to NM_032206.3 T846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr16:57067575 G>A maps to NM_032206.3 T846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr16:84163847 G>A maps to NM_031463.4 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr16:84163847 G>A maps to NM_031463.4 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr17:3926062 C>G maps to NM_015113.3 L2384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr17:3926062 C>G maps to NM_015113.3 L2384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr17:12905652 C>A maps to NM_018127.6 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr17:12905652 C>A maps to NM_018127.6 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr17:46051294 A>G did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr17:46051294 A>G did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr17:71390386 G>A maps to NM_001144952.1 V1223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr17:71390386 G>A maps to NM_001144952.1 V1223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr18:50450074 A>G did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr18:50450074 A>G did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr19:9086083 G>A maps to NM_024690.2 R1911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr19:9086083 G>A maps to NM_024690.2 R1911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr19:38976616 G>A maps to NM_000540.2 P1774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr19:38976616 G>A maps to NM_000540.2 P1774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr19:39100272 G>C maps to NM_001042600.1 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr19:39100272 G>C maps to NM_001042600.1 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr19:44515024 G>A maps to NM_006300.3 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr19:44515024 G>A maps to NM_006300.3 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr19:46973548 C>T maps to NM_018215.3 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr19:46973548 C>T maps to NM_018215.3 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr19:48202268 C>T maps to NM_015711.3 Q1149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr19:48202268 C>T maps to NM_015711.3 Q1149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr19:50098458 C>T maps to NM_020719.1 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr19:50098458 C>T maps to NM_020719.1 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr2:111416239 C>T maps to NM_004336.3 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr2:111416239 C>T maps to NM_004336.3 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr2:166172117 A>G maps to NM_001040142.1 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr2:166172117 A>G maps to NM_001040142.1 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr2:179650466 G>A maps to NM_133378.4 I791I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr2:179650466 G>A maps to NM_133378.4 I791I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr2:197737750 C>A did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr2:197737750 C>A did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr20:8741078 A>G maps to NM_015192.2 T894T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr20:8741078 A>G maps to NM_015192.2 T894T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr21:32582411 C>G maps to NM_003253.2 T779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr21:32582411 C>G maps to NM_003253.2 T779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr21:32638553 T>G maps to NM_003253.2 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr21:32638553 T>G maps to NM_003253.2 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr21:45815334 C>A maps to ENST00000397932 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr21:45815334 C>A maps to ENST00000397932 S611S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr22:23438556 T>C maps to NM_002073.2 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr22:23438556 T>C maps to NM_002073.2 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr22:30887557 A>G did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr22:30887557 A>G did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr3:71019956 C>T did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr3:71019956 C>T did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr3:168838940 G>T maps to NM_004991.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr3:168838940 G>T maps to NM_004991.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr3:193332568 A>T maps to NM_130837.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr3:193332568 A>T maps to NM_130837.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr5:79855682 C>T maps to NM_001004441.2 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr5:79855682 C>T maps to NM_001004441.2 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr5:140866932 T>C maps to NM_018928.2 C731C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr5:140866932 T>C maps to NM_018928.2 C731C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr6:26271402 G>A maps to NM_003534.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr6:26271402 G>A maps to NM_003534.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr6:29407953 C>A maps to NM_013941.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr6:29407953 C>A maps to NM_013941.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr6:89862894 A>T maps to NM_001010853.1 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr6:89862894 A>T maps to NM_001010853.1 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr6:167595388 G>A maps to NM_001145121.1 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr6:167595388 G>A maps to NM_001145121.1 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr7:73183872 G>T maps to NM_001306.3 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr7:73183872 G>T maps to NM_001306.3 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr7:75988083 G>T maps to NM_012479.3 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr7:75988083 G>T maps to NM_012479.3 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr7:76140091 C>A maps to NM_030570.2 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr7:76140091 C>A maps to NM_030570.2 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr7:82996903 A>G maps to NM_012431.2 *776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr7:82996903 A>G maps to NM_012431.2 *776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr8:27779352 G>A maps to NM_173833.5 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr8:27779352 G>A maps to NM_173833.5 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr8:30546803 C>T maps to NM_000637.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr8:30546803 C>T maps to NM_000637.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr9:34635730 G>C maps to NM_005866.2 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr9:34635730 G>C maps to NM_005866.2 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr9:85616026 A>T maps to NM_152573.2 Y407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr9:85616026 A>T maps to NM_152573.2 Y407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr9:95027218 G>C maps to ENST00000375660 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chr9:95027218 G>C maps to ENST00000375660 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chrX:14708938 G>A maps to NM_002063.3 K346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chrX:14708938 G>A maps to NM_002063.3 K346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chrX:105178436 G>T did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chrX:105178436 G>T did not map to a codon.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chrX:151806745 G>A maps to NM_018558.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chrX:151806745 G>A maps to NM_018558.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chrX:152226118 T>A maps to NM_013364.4 L236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chrX:152226118 T>A maps to NM_013364.4 L236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chrX:155233506 G>T maps to NM_002186.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6995-01A-31D-2012-08 chrX:155233506 G>T maps to NM_002186.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr1:78433857 G>A maps to ENST00000436586 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr1:78433857 G>A maps to ENST00000436586 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr1:186648487 G>A maps to NM_000963.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr1:186648487 G>A maps to NM_000963.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr1:235324258 G>C maps to NM_015014.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr1:235324258 G>C maps to NM_015014.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr10:52576012 G>A maps to NM_138932.2 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr10:52576012 G>A maps to NM_138932.2 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr11:62293149 T>C maps to NM_001620.1 E2913E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr11:62293149 T>C maps to NM_001620.1 E2913E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr12:112150387 G>A maps to NM_001136538.1 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr12:112150387 G>A maps to NM_001136538.1 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr14:58605874 G>A maps to ENST00000438670 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr14:58605874 G>A maps to ENST00000438670 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr16:27561046 C>T maps to NM_001520.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr16:27561046 C>T maps to NM_001520.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr19:14591279 G>A maps to NM_202470.1 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr19:14591279 G>A maps to NM_202470.1 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr2:11053826 C>T maps to NM_002236.4 H425H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr2:11053826 C>T maps to NM_002236.4 H425H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr2:27715570 C>A maps to NM_022823.2 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr2:27715570 C>A maps to NM_022823.2 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr2:74654584 C>T maps to NM_001015055.1 W407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr2:74654584 C>T maps to NM_001015055.1 W407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr2:112821763 T>C maps to NM_032824.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr2:112821763 T>C maps to NM_032824.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr20:2816811 C>T maps to NM_022760.3 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr20:2816811 C>T maps to NM_022760.3 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr20:47266744 C>T did not map to a codon.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr20:47266744 C>T did not map to a codon.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr22:46725346 C>T maps to NM_016426.6 C673C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr22:46725346 C>T maps to NM_016426.6 C673C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr3:138383966 A>C maps to NM_006219.1 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr3:138383966 A>C maps to NM_006219.1 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr4:113533742 C>G maps to NM_018392.4 V868V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr4:113533742 C>G maps to NM_018392.4 V868V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr7:34118793 A>G maps to NM_133468.3 K468K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr7:34118793 A>G maps to NM_133468.3 K468K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr9:21971207 C>T did not map to a codon.
Sequencing variant TCGA-CN-6996-01A-11D-1912-08 chr9:21971207 C>T did not map to a codon.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr1:1686105 C>T maps to ENST00000344463 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr1:1686105 C>T maps to ENST00000344463 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr1:16258888 A>T maps to NM_015001.2 K2052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr1:16258888 A>T maps to NM_015001.2 K2052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr1:85733453 G>A maps to NM_003921.4 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr1:85733453 G>A maps to NM_003921.4 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr1:201356296 G>A maps to NM_005558.3 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr1:201356296 G>A maps to NM_005558.3 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr10:70514523 T>A maps to NM_018237.2 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr10:70514523 T>A maps to NM_018237.2 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr10:70728813 A>G maps to NM_004728.2 K391K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr10:70728813 A>G maps to NM_004728.2 K391K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr11:1261155 G>A maps to ENST00000447027 A1240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr11:1261155 G>A maps to ENST00000447027 A1240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr11:20126981 A>G did not map to a codon.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr11:20126981 A>G did not map to a codon.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr11:55322552 G>T maps to NM_001001920.1 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr11:55322552 G>T maps to NM_001001920.1 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr11:89070671 C>T maps to NM_016931.3 E486E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr11:89070671 C>T maps to NM_016931.3 E486E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr11:108380449 G>A maps to NM_015065.2 N1928N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr11:108380449 G>A maps to NM_015065.2 N1928N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr11:121058639 C>T maps to NM_005422.2 Y2033Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr11:121058639 C>T maps to NM_005422.2 Y2033Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr12:6438513 G>A maps to NM_001065.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr12:6438513 G>A maps to NM_001065.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr12:25047337 T>G maps to NM_001178093.1 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr12:25047337 T>G maps to NM_001178093.1 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr13:23905801 T>C maps to NM_014363.4 E4071E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr13:23905801 T>C maps to NM_014363.4 E4071E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr13:32798393 G>A maps to NM_023037.2 T1596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr13:32798393 G>A maps to NM_023037.2 T1596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr13:92408603 C>T maps to NM_004466.4 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr13:92408603 C>T maps to NM_004466.4 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr15:72534498 T>C maps to NM_020214.2 E568E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr15:72534498 T>C maps to NM_020214.2 E568E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr16:24196443 C>T maps to NM_002738.6 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr16:24196443 C>T maps to NM_002738.6 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr16:24580071 A>G maps to NM_006910.4 K687K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr16:24580071 A>G maps to NM_006910.4 K687K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr16:51171061 G>C maps to ENST00000251020 T1312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr16:51171061 G>C maps to ENST00000251020 T1312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr16:67682064 C>A maps to NM_001013838.1 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr16:67682064 C>A maps to NM_001013838.1 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr16:68336299 T>C maps to NM_032178.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr16:68336299 T>C maps to NM_032178.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr17:7578523 G>A maps to NM_001126112.1 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr17:7578523 G>A maps to NM_001126112.1 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr17:10364245 T>A maps to NM_017533.2 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr17:10364245 T>A maps to NM_017533.2 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr17:48916921 C>A maps to NM_175575.5 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr17:48916921 C>A maps to NM_175575.5 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr19:1556344 G>A maps to NM_001174118.1 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr19:1556344 G>A maps to NM_001174118.1 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr19:10823849 C>T maps to NM_031209.2 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr19:10823849 C>T maps to NM_031209.2 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr19:55085311 C>G did not map to a codon.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr19:55085311 C>G did not map to a codon.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr2:79385862 G>T maps to NM_138937.2 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr2:79385862 G>T maps to NM_138937.2 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr2:103274383 C>A maps to NM_003048.3 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr2:103274383 C>A maps to NM_003048.3 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr2:187506310 C>T maps to NM_002210.3 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr2:187506310 C>T maps to NM_002210.3 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr3:51743448 G>A maps to NM_000839.3 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr3:51743448 G>A maps to NM_000839.3 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr3:100963027 G>C maps to NM_016247.2 S716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr3:100963027 G>C maps to NM_016247.2 S716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr3:140998226 C>T maps to NM_001037172.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr3:140998226 C>T maps to NM_001037172.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr5:168112760 G>A maps to NM_003062.2 F1162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr5:168112760 G>A maps to NM_003062.2 F1162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr6:130505271 G>A maps to ENST00000457563 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr6:130505271 G>A maps to ENST00000457563 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr7:72413672 C>T maps to ENST00000434423 F1047F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr7:72413672 C>T maps to ENST00000434423 F1047F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr7:87910250 C>T maps to NM_024636.2 W376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr7:87910250 C>T maps to NM_024636.2 W376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr8:15601045 G>T did not map to a codon.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr8:15601045 G>T did not map to a codon.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr9:74332990 G>A maps to NM_013390.2 R758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr9:74332990 G>A maps to NM_013390.2 R758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr9:100090305 G>T maps to ENST00000375206 E739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6997-01A-11D-2012-08 chr9:100090305 G>T maps to ENST00000375206 E739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr1:15956838 C>T maps to NM_032341.4 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr1:15956838 C>T maps to NM_032341.4 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr1:53972292 C>T maps to NM_147193.2 *621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr1:53972292 C>T maps to NM_147193.2 *621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr1:154179929 C>G maps to NM_001098616.1 *254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr1:154179929 C>G maps to NM_001098616.1 *254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr1:156628470 C>T maps to NM_021948.3 C858C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr1:156628470 C>T maps to NM_021948.3 C858C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr1:176833524 G>A maps to ENST00000281881 P1268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr1:176833524 G>A maps to ENST00000281881 P1268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr11:61533489 G>A maps to NM_001127392.1 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr11:61533489 G>A maps to NM_001127392.1 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr11:77937652 G>A maps to NM_080491.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr11:77937652 G>A maps to NM_080491.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr12:9840538 C>T maps to NM_001004419.3 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr12:9840538 C>T maps to NM_001004419.3 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr12:101491681 G>T maps to ENST00000392977 V655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr12:101491681 G>T maps to ENST00000392977 V655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr12:125397195 C>T maps to NM_021009.5 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr12:125397195 C>T maps to NM_021009.5 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr14:94088225 A>G maps to ENST00000393153 R1571R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr14:94088225 A>G maps to ENST00000393153 R1571R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr16:51174767 C>T maps to ENST00000251020 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr16:51174767 C>T maps to ENST00000251020 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr17:18022713 C>T maps to ENST00000205890 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr17:18022713 C>T maps to ENST00000205890 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr17:56352926 C>T maps to ENST00000340482 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr17:56352926 C>T maps to ENST00000340482 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr19:5641945 C>T maps to ENST00000433404 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr19:5641945 C>T maps to ENST00000433404 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr19:44223072 G>A maps to NM_019612.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr19:44223072 G>A maps to NM_019612.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr19:51914353 C>T maps to NM_033130.4 *698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr19:51914353 C>T maps to NM_033130.4 *698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr2:7027108 C>T maps to NM_080657.4 D184D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr2:7027108 C>T maps to NM_080657.4 D184D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr2:233899355 C>T maps to NM_005383.2 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr2:233899355 C>T maps to NM_005383.2 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr20:60584188 A>T maps to NM_003185.3 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr20:60584188 A>T maps to NM_003185.3 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr3:33195133 G>A maps to NM_015551.1 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr3:33195133 G>A maps to NM_015551.1 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr3:56651599 G>A maps to NM_001141947.1 T768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr3:56651599 G>A maps to NM_001141947.1 T768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr3:74315640 G>A maps to NM_020872.1 R993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr3:74315640 G>A maps to NM_020872.1 R993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr3:113659106 C>G maps to NM_017577.4 S608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr3:113659106 C>G maps to NM_017577.4 S608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr3:192516653 G>T maps to NM_178496.3 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr3:192516653 G>T maps to NM_178496.3 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr4:74351713 C>T maps to NM_001133.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr4:74351713 C>T maps to NM_001133.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr4:111397713 C>T maps to NM_001977.3 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr4:111397713 C>T maps to NM_001977.3 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr4:187454890 C>T maps to NM_005958.3 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr4:187454890 C>T maps to NM_005958.3 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr5:908534 C>T maps to NM_004237.3 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr5:908534 C>T maps to NM_004237.3 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr5:7870927 A>G maps to NM_024010.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr5:7870927 A>G maps to NM_024010.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr5:71494371 G>A maps to NM_005909.3 P1730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr5:71494371 G>A maps to NM_005909.3 P1730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr5:140503124 C>T maps to NM_018938.2 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr5:140503124 C>T maps to NM_018938.2 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr6:26199447 G>A maps to NM_021065.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr6:26199447 G>A maps to NM_021065.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr6:170156466 C>T maps to NM_018341.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr6:170156466 C>T maps to NM_018341.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr7:1517525 C>A maps to ENST00000389470 L1774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr7:1517525 C>A maps to ENST00000389470 L1774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr7:29105713 G>A maps to NM_031311.3 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr7:29105713 G>A maps to NM_031311.3 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr7:149486776 C>T maps to NM_198455.2 C1518C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr7:149486776 C>T maps to NM_198455.2 C1518C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr7:151891213 C>G did not map to a codon.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr7:151891213 C>G did not map to a codon.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr8:87638273 C>T maps to NM_019098.4 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr8:87638273 C>T maps to NM_019098.4 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chrX:32591888 G>C maps to ENST00000357033 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6998-01A-23D-2012-08 chrX:32591888 G>C maps to ENST00000357033 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr1:211652473 G>A maps to NM_183059.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr1:211652473 G>A maps to NM_183059.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr10:27687276 G>A maps to NM_001034842.3 F750F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr10:27687276 G>A maps to NM_001034842.3 F750F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr10:29581595 C>T maps to NM_032517.4 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr10:29581595 C>T maps to NM_032517.4 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr10:70405629 C>A maps to NM_030625.2 C1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr10:70405629 C>A maps to NM_030625.2 C1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr10:86131077 T>C maps to ENST00000372088 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr10:86131077 T>C maps to ENST00000372088 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr10:134008355 C>T maps to NM_006426.2 H107H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr10:134008355 C>T maps to NM_006426.2 H107H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr11:1309865 G>A maps to ENST00000382211 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr11:1309865 G>A maps to ENST00000382211 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr11:65623572 G>A maps to NM_005507.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr11:65623572 G>A maps to NM_005507.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr11:65623575 G>A maps to NM_005507.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr11:65623575 G>A maps to NM_005507.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr12:49447021 C>A maps to NM_003482.3 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr12:49447021 C>A maps to NM_003482.3 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr17:6599180 G>T maps to NM_177550.3 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr17:6599180 G>T maps to NM_177550.3 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr17:39118799 G>A maps to NM_213656.3 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr17:39118799 G>A maps to NM_213656.3 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr17:57125152 G>A maps to NM_015294.3 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr17:57125152 G>A maps to NM_015294.3 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr2:198636707 T>G did not map to a codon.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr2:198636707 T>G did not map to a codon.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr22:38119915 C>T maps to NM_001039141.2 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr22:38119915 C>T maps to NM_001039141.2 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr22:40817049 C>A maps to NM_020831.3 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr22:40817049 C>A maps to NM_020831.3 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr22:41173339 C>T maps to NM_006358.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr22:41173339 C>T maps to NM_006358.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr22:50903691 G>T maps to ENST00000337034 C395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr22:50903691 G>T maps to ENST00000337034 C395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr3:40085594 G>A maps to NM_015460.2 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr3:40085594 G>A maps to NM_015460.2 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr3:178543543 G>A maps to NM_005832.3 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr3:178543543 G>A maps to NM_005832.3 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr3:195792458 T>C maps to NM_001128148.1 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr3:195792458 T>C maps to NM_001128148.1 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr4:162307360 C>T maps to NM_020116.3 T694T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr4:162307360 C>T maps to NM_020116.3 T694T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr8:110447467 C>T maps to ENST00000426474 P1130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr8:110447467 C>T maps to ENST00000426474 P1130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr9:94486330 C>T maps to NM_004560.2 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr9:94486330 C>T maps to NM_004560.2 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr9:95609542 G>T maps to NM_031486.1 S509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr9:95609542 G>T maps to NM_031486.1 S509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr9:101470779 G>A maps to NM_005458.7 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr9:101470779 G>A maps to NM_005458.7 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr9:132740854 G>A maps to NM_015033.2 N78N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5323-01A-01D-1683-08 chr9:132740854 G>A maps to NM_015033.2 N78N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr1:16559456 G>A maps to NM_030907.3 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr1:16559456 G>A maps to NM_030907.3 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr1:19596119 G>A maps to NM_201252.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr1:19596119 G>A maps to NM_201252.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr1:27682187 G>A maps to NM_004672.3 R1254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr1:27682187 G>A maps to NM_004672.3 R1254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr11:63668101 G>A maps to NM_001039469.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr11:63668101 G>A maps to NM_001039469.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr13:28771371 A>T maps to NM_175854.7 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr13:28771371 A>T maps to NM_175854.7 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr13:43597851 C>T maps to NM_013238.2 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr13:43597851 C>T maps to NM_013238.2 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr14:21499179 C>T maps to NM_173846.4 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr14:21499179 C>T maps to NM_173846.4 N61N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr17:29657374 C>T maps to NM_001042492.2 Q1891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr17:29657374 C>T maps to NM_001042492.2 Q1891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr19:45774926 C>T maps to NM_031417.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr19:45774926 C>T maps to NM_031417.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr19:56203253 C>T maps to NM_001130071.1 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr19:56203253 C>T maps to NM_001130071.1 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr2:15557649 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr2:15557649 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr20:44439537 C>T maps to NM_052951.2 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr20:44439537 C>T maps to NM_052951.2 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr21:32639126 C>G maps to NM_003253.2 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr21:32639126 C>G maps to NM_003253.2 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr21:32639147 C>T maps to NM_003253.2 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr21:32639147 C>T maps to NM_003253.2 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr21:38538337 C>G maps to NM_003316.3 V1274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr21:38538337 C>G maps to NM_003316.3 V1274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr3:47163753 G>C maps to NM_014159.6 S791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr3:47163753 G>C maps to NM_014159.6 S791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr3:132423040 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr3:132423040 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr5:75991295 G>A maps to NM_006633.2 T1337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr5:75991295 G>A maps to NM_006633.2 T1337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr5:149901142 C>T maps to NM_001543.4 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr5:149901142 C>T maps to NM_001543.4 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr6:32714065 C>T maps to NM_020056.4 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr6:32714065 C>T maps to NM_020056.4 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr6:47846395 G>A maps to NM_001013732.3 H728H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr6:47846395 G>A maps to NM_001013732.3 H728H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr6:150005728 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr6:150005728 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr8:97311962 G>A maps to NM_014754.1 W214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chr8:97311962 G>A maps to NM_014754.1 W214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chrX:34962351 G>A maps to NM_152631.2 W468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5324-01A-01D-1683-08 chrX:34962351 G>A maps to NM_152631.2 W468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr1:27697412 G>A maps to NM_003665.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr1:27697412 G>A maps to NM_003665.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr10:105821184 G>A maps to NM_000494.3 N319N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr10:105821184 G>A maps to NM_000494.3 N319N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr10:115601163 C>G did not map to a codon.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr10:115601163 C>G did not map to a codon.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr11:6290926 T>G maps to NM_176875.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr11:6290926 T>G maps to NM_176875.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr12:25671776 A>G maps to NM_001145728.1 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr12:25671776 A>G maps to NM_001145728.1 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr12:123475221 T>C maps to NM_020845.2 Q813Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr12:123475221 T>C maps to NM_020845.2 Q813Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr14:31122763 G>A maps to ENST00000311943 W283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr14:31122763 G>A maps to ENST00000311943 W283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr17:17150426 T>A maps to NM_003653.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr17:17150426 T>A maps to NM_003653.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr19:40872531 G>T maps to NM_012268.2 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr19:40872531 G>T maps to NM_012268.2 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr4:56316288 T>C maps to NM_004898.2 K439K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr4:56316288 T>C maps to NM_004898.2 K439K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr4:109667915 A>C did not map to a codon.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr4:109667915 A>C did not map to a codon.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr7:111368575 C>T maps to ENST00000428084 P1894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr7:111368575 C>T maps to ENST00000428084 P1894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr7:129986246 G>A did not map to a codon.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr7:129986246 G>A did not map to a codon.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr7:152346253 C>A maps to NM_005431.1 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr7:152346253 C>A maps to NM_005431.1 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr8:33310866 G>A maps to ENST00000380081 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr8:33310866 G>A maps to ENST00000380081 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr8:54764581 C>T maps to NM_170587.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr8:54764581 C>T maps to NM_170587.2 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr9:6328606 C>G maps to NM_033516.5 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chr9:6328606 C>G maps to NM_033516.5 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chrX:31947846 A>G maps to ENST00000357033 L2260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5325-01A-01D-1683-08 chrX:31947846 A>G maps to ENST00000357033 L2260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:2077509 C>T maps to NM_002744.4 N199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:2077509 C>T maps to NM_002744.4 N199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:3334403 G>T maps to NM_022114.3 E902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:3334403 G>T maps to NM_022114.3 E902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:6528528 G>C maps to NM_198681.2 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:6528528 G>C maps to NM_198681.2 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:10434487 C>T maps to ENST00000377086 L1687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:10434487 C>T maps to ENST00000377086 L1687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:16893672 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:16893672 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:25944443 C>G maps to NM_020379.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:25944443 C>G maps to NM_020379.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:32210288 C>T maps to NM_001703.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:32210288 C>T maps to NM_001703.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:39753029 C>T maps to ENST00000361689 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:39753029 C>T maps to ENST00000361689 F532F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:79387471 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:79387471 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:97235415 G>C maps to ENST00000370197 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:97235415 G>C maps to ENST00000370197 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:153043108 C>T maps to NM_001017418.1 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:153043108 C>T maps to NM_001017418.1 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:166039588 C>T maps to NM_001017961.3 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:166039588 C>T maps to NM_001017961.3 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:248028107 G>A maps to NM_015431.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr1:248028107 G>A maps to NM_015431.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:14816384 G>C maps to NM_031453.2 S93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:14816384 G>C maps to NM_031453.2 S93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:48390445 C>G maps to NM_002900.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:48390445 C>G maps to NM_002900.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:50819199 G>C maps to NM_003055.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:50819199 G>C maps to NM_003055.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:55566625 C>A maps to ENST00000373965 E1590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:55566625 C>A maps to ENST00000373965 E1590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:55826606 G>C maps to NM_001142763.1 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:55826606 G>C maps to NM_001142763.1 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:75855483 G>A maps to NM_014000.2 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:75855483 G>A maps to NM_014000.2 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:102054859 G>A maps to NM_016112.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:102054859 G>A maps to NM_016112.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:106014945 G>A maps to NM_004832.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:106014945 G>A maps to NM_004832.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:126682515 G>A maps to NM_022802.2 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr10:126682515 G>A maps to NM_022802.2 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:399092 C>G maps to NM_007183.2 Y390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:399092 C>G maps to NM_007183.2 Y390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:5529405 A>G maps to NM_017481.2 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:5529405 A>G maps to NM_017481.2 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:49186310 C>T maps to NM_004476.1 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:49186310 C>T maps to NM_004476.1 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:51411716 G>A maps to NM_001005272.3 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:51411716 G>A maps to NM_001005272.3 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:67271645 G>T maps to NM_004910.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:67271645 G>T maps to NM_004910.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:67818100 C>A maps to NM_006019.3 S795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:67818100 C>A maps to NM_006019.3 S795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:68197130 C>G maps to NM_002335.2 V1242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:68197130 C>G maps to NM_002335.2 V1242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:117186310 C>G maps to NM_012104.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:117186310 C>G maps to NM_012104.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:121478811 G>A did not map to a codon.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:121478811 G>A did not map to a codon.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr12:48526695 C>T maps to NM_001166686.1 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr12:48526695 C>T maps to NM_001166686.1 R166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr12:110236714 C>A maps to NM_021625.4 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr12:110236714 C>A maps to NM_021625.4 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr12:122748186 C>T maps to NM_022916.4 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr12:122748186 C>T maps to NM_022916.4 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr12:123444338 C>T maps to NM_203444.2 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr12:123444338 C>T maps to NM_203444.2 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr13:73320741 G>A maps to ENST00000377815 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr13:73320741 G>A maps to ENST00000377815 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr13:111980539 T>C maps to NM_152324.1 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr13:111980539 T>C maps to NM_152324.1 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr14:80130177 G>T maps to NM_004796.4 E795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr14:80130177 G>T maps to NM_004796.4 E795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr14:92136189 G>A maps to NM_024764.2 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr14:92136189 G>A maps to NM_024764.2 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr15:43687328 G>T maps to ENST00000399460 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr15:43687328 G>T maps to ENST00000399460 E347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr16:1399475 C>A maps to NM_001001410.2 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr16:1399475 C>A maps to NM_001001410.2 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr16:55844471 C>G maps to NM_001025195.1 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr16:55844471 C>G maps to NM_001025195.1 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr17:1787117 A>G maps to NM_002945.3 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr17:1787117 A>G maps to NM_002945.3 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr17:7579697 A>C did not map to a codon.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr17:7579697 A>C did not map to a codon.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr17:28788938 G>A maps to NM_001304.4 K1225K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr17:28788938 G>A maps to NM_001304.4 K1225K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr17:41256888 C>T maps to ENST00000471181 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr17:41256888 C>T maps to ENST00000471181 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr17:47797211 G>A maps to NM_030802.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr17:47797211 G>A maps to NM_030802.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr17:73698630 G>A maps to NM_013260.6 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr17:73698630 G>A maps to NM_013260.6 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:10090690 G>A maps to NM_015719.3 F879F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:10090690 G>A maps to NM_015719.3 F879F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:10090710 G>A maps to NM_015719.3 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:10090710 G>A maps to NM_015719.3 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:11145804 C>G maps to NM_001128849.1 L1389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:11145804 C>G maps to NM_001128849.1 L1389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:11978655 C>T maps to NM_152262.2 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:11978655 C>T maps to NM_152262.2 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:15769191 C>A maps to NM_000896.2 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:15769191 C>A maps to NM_000896.2 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:18729055 C>T maps to NM_012109.2 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:18729055 C>T maps to NM_012109.2 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:22156014 T>C maps to NM_007153.3 K607K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:22156014 T>C maps to NM_007153.3 K607K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:38800242 G>A maps to NM_001039672.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:38800242 G>A maps to NM_001039672.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:42799109 G>T maps to NM_015125.3 E1532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr19:42799109 G>T maps to NM_015125.3 E1532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:27609063 C>T maps to NM_177983.1 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:27609063 C>T maps to NM_177983.1 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:27680752 C>T maps to NM_015662.1 K1022K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:27680752 C>T maps to NM_015662.1 K1022K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:54112829 G>A maps to NM_014614.2 F1604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:54112829 G>A maps to NM_014614.2 F1604F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:65492282 T>C maps to NM_001005386.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:65492282 T>C maps to NM_001005386.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:69002482 G>A maps to NM_001007231.2 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:69002482 G>A maps to NM_001007231.2 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:101881352 T>C maps to NM_017546.4 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:101881352 T>C maps to NM_017546.4 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:160019982 C>G maps to NM_033394.2 S291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:160019982 C>G maps to NM_033394.2 S291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:179412920 C>T maps to NM_133378.4 R28576R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:179412920 C>T maps to NM_133378.4 R28576R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:191845387 G>A maps to NM_007315.3 N530N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:191845387 G>A maps to NM_007315.3 N530N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:201757019 G>A maps to NM_001136039.2 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr2:201757019 G>A maps to NM_001136039.2 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr20:58514188 G>C maps to NM_006242.3 Y266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr20:58514188 G>C maps to NM_006242.3 Y266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr20:62738004 C>G maps to NM_005286.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr20:62738004 C>G maps to NM_005286.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr21:34903797 C>T maps to NM_001136006.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr21:34903797 C>T maps to NM_001136006.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr22:39883474 C>T maps to NM_001098270.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr22:39883474 C>T maps to NM_001098270.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr22:51137178 C>T maps to NM_001080420.1 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr22:51137178 C>T maps to NM_001080420.1 F536F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr3:52675990 C>A maps to ENST00000296302 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr3:52675990 C>A maps to ENST00000296302 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr3:121641669 C>T maps to NM_021082.3 R277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr3:121641669 C>T maps to NM_021082.3 R277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr3:132086632 C>G maps to NM_001134194.1 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr3:132086632 C>G maps to NM_001134194.1 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr4:3219627 C>T maps to NM_002111.6 I2397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr4:3219627 C>T maps to NM_002111.6 I2397I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr4:85414576 G>A maps to NM_006168.2 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr4:85414576 G>A maps to NM_006168.2 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr5:173359490 C>T maps to NM_030627.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr5:173359490 C>T maps to NM_030627.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr5:179260065 G>A maps to NM_003900.4 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr5:179260065 G>A maps to NM_003900.4 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr6:10707719 C>A maps to NM_017906.2 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr6:10707719 C>A maps to NM_017906.2 I271I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CQ-5326-01A-01D-1870-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CQ-5326-01A-01D-1870-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr6:35773542 C>T maps to NM_182548.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr6:35773542 C>T maps to NM_182548.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr6:46793144 G>A maps to NM_005588.2 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr6:46793144 G>A maps to NM_005588.2 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr6:46826147 G>C maps to NM_015234.4 L1164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr6:46826147 G>C maps to NM_015234.4 L1164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr6:111697183 G>A maps to NM_002912.3 Q792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr6:111697183 G>A maps to NM_002912.3 Q792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr6:112671179 C>G maps to NM_001013734.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr6:112671179 C>G maps to NM_001013734.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr6:137245832 G>C maps to NM_001008783.1 *417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr6:137245832 G>C maps to NM_001008783.1 *417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr7:6730808 C>T maps to ENST00000330442 Q645Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr7:6730808 C>T maps to ENST00000330442 Q645Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr7:34118697 C>G maps to NM_133468.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr7:34118697 C>G maps to NM_133468.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr7:70255919 C>T maps to NM_015570.2 L1240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr7:70255919 C>T maps to NM_015570.2 L1240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr7:80418763 A>G maps to NM_006379.2 H404H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr7:80418763 A>G maps to NM_006379.2 H404H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr7:143807022 G>A maps to NM_001005480.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr7:143807022 G>A maps to NM_001005480.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr8:80577107 G>A maps to NM_007029.3 *180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr8:80577107 G>A maps to NM_007029.3 *180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr9:114986136 T>C maps to NM_001163790.1 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr9:114986136 T>C maps to NM_001163790.1 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr9:130828915 G>A maps to NM_197956.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr9:130828915 G>A maps to NM_197956.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr9:134501393 G>A maps to NM_198679.1 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr9:134501393 G>A maps to NM_198679.1 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chrX:2838723 G>A maps to NM_001669.2 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chrX:2838723 G>A maps to NM_001669.2 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chrX:48979985 C>G maps to NM_015698.4 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chrX:48979985 C>G maps to NM_015698.4 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chrX:77365366 C>G maps to NM_000291.3 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chrX:77365366 C>G maps to NM_000291.3 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chrX:106391015 C>T maps to ENST00000372465 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chrX:106391015 C>T maps to ENST00000372465 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chrX:125685628 G>A maps to NM_178470.4 Y321Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chrX:125685628 G>A maps to NM_178470.4 Y321Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chrX:128710496 C>T maps to NM_000276.3 R695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chrX:128710496 C>T maps to NM_000276.3 R695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr1:43630161 C>T maps to NM_001159936.1 K346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr1:43630161 C>T maps to NM_001159936.1 K346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr1:89579770 C>T maps to NM_004120.3 E359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr1:89579770 C>T maps to NM_004120.3 E359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr1:145015937 C>T maps to NM_001198832.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr1:145015937 C>T maps to NM_001198832.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr1:152083790 C>T maps to NM_007113.2 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr1:152083790 C>T maps to NM_007113.2 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr1:156233277 G>A maps to NM_015327.2 Q647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr1:156233277 G>A maps to NM_015327.2 Q647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr1:162326886 C>G maps to NM_014697.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr1:162326886 C>G maps to NM_014697.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr10:267289 T>C maps to NM_006624.4 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr10:267289 T>C maps to NM_006624.4 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr10:105005974 C>A maps to NM_001143909.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr10:105005974 C>A maps to NM_001143909.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:280966 G>A maps to NM_138329.1 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:280966 G>A maps to NM_138329.1 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:11964240 T>C maps to ENST00000399455 P898P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:11964240 T>C maps to ENST00000399455 P898P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:18633880 G>A maps to NM_194285.2 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:18633880 G>A maps to NM_194285.2 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:62289229 G>C maps to NM_001620.1 S4220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:62289229 G>C maps to NM_001620.1 S4220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:64521494 C>T maps to NM_005609.2 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:64521494 C>T maps to NM_005609.2 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:85779726 G>A maps to ENST00000393343 H32H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:85779726 G>A maps to ENST00000393343 H32H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:86868384 C>T maps to NM_022918.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:86868384 C>T maps to NM_022918.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:119181848 G>A maps to NM_006500.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:119181848 G>A maps to NM_006500.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:129772279 C>T maps to NM_020228.2 Q1137Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr11:129772279 C>T maps to NM_020228.2 Q1137Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr12:21794925 G>A maps to NM_002300.6 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr12:21794925 G>A maps to NM_002300.6 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr12:41374735 G>C maps to NM_001843.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr12:41374735 G>C maps to NM_001843.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr12:53664559 G>A maps to NM_012291.4 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr12:53664559 G>A maps to NM_012291.4 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr13:33701583 G>A maps to NM_178007.2 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr13:33701583 G>A maps to NM_178007.2 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr14:23451249 G>A maps to NM_032876.4 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr14:23451249 G>A maps to NM_032876.4 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr14:23451382 G>A maps to NM_032876.4 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr14:23451382 G>A maps to NM_032876.4 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr14:105174902 G>A maps to ENST00000252520 R622R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr14:105174902 G>A maps to ENST00000252520 R622R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr16:1741946 C>T maps to ENST00000382711 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr16:1741946 C>T maps to ENST00000382711 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr16:21011750 G>A maps to NM_017539.1 F2072F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr16:21011750 G>A maps to NM_017539.1 F2072F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr16:23570849 G>A maps to ENST00000219638 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr16:23570849 G>A maps to ENST00000219638 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr16:67005130 G>T maps to NM_024922.5 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr16:67005130 G>T maps to NM_024922.5 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr16:67912723 C>T maps to NM_014329.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr16:67912723 C>T maps to NM_014329.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr17:18045515 C>T maps to ENST00000205890 L1925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr17:18045515 C>T maps to ENST00000205890 L1925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr17:39580457 C>T maps to NM_003770.4 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr17:39580457 C>T maps to NM_003770.4 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr17:40063715 G>A maps to ENST00000401700 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr17:40063715 G>A maps to ENST00000401700 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr17:73831828 C>T maps to ENST00000412096 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr17:73831828 C>T maps to ENST00000412096 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr17:73998156 C>T maps to NM_001258.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr17:73998156 C>T maps to NM_001258.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr18:64176483 C>G did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr18:64176483 C>G did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:6495567 G>A maps to NM_006087.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:6495567 G>A maps to NM_006087.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:7968930 C>T maps to ENST00000425613 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:7968930 C>T maps to ENST00000425613 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:10747141 C>T maps to NM_020428.3 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:10747141 C>T maps to NM_020428.3 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:12721449 G>A maps to NM_020714.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:12721449 G>A maps to NM_020714.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:36357324 C>T maps to NM_199180.2 P686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:36357324 C>T maps to NM_199180.2 P686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:36558320 C>T maps to NM_001083961.1 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:36558320 C>T maps to NM_001083961.1 F225F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:45910391 G>A maps to ENST00000423698 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:45910391 G>A maps to ENST00000423698 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:56154206 C>T maps to NM_001163423.1 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr19:56154206 C>T maps to NM_001163423.1 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:15519751 G>C maps to NM_015909.2 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:15519751 G>C maps to NM_015909.2 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:26533571 G>C maps to NM_001145168.1 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:26533571 G>C maps to NM_001145168.1 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:26533787 G>A maps to NM_001145168.1 I936I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:26533787 G>A maps to NM_001145168.1 I936I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:44128663 C>G did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:44128663 C>G did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:55561401 A>T maps to ENST00000436346 L852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:55561401 A>T maps to ENST00000436346 L852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:70315831 G>A maps to NM_006196.3 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:70315831 G>A maps to NM_006196.3 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:97035189 C>G maps to NM_015341.3 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:97035189 C>G maps to NM_015341.3 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:101624354 G>A maps to NM_001102426.1 I1117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:101624354 G>A maps to NM_001102426.1 I1117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:179638441 C>G maps to NM_133378.4 V2447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr2:179638441 C>G maps to NM_133378.4 V2447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr20:2375140 C>T maps to NM_198994.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr20:2375140 C>T maps to NM_198994.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr20:9547018 G>A maps to NM_177990.2 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr20:9547018 G>A maps to NM_177990.2 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr20:60883182 G>A maps to NM_175573.1 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr20:60883182 G>A maps to NM_175573.1 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr21:31812665 T>A maps to NM_181623.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr21:31812665 T>A maps to NM_181623.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr21:33067130 G>A maps to NM_020706.2 Q411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr21:33067130 G>A maps to NM_020706.2 Q411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr22:37407205 G>A maps to NM_003312.4 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr22:37407205 G>A maps to NM_003312.4 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr22:41547911 C>T maps to NM_001429.3 Q965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr22:41547911 C>T maps to NM_001429.3 Q965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr22:43924775 G>C maps to NM_022785.3 S1488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr22:43924775 G>C maps to NM_022785.3 S1488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr3:39228920 G>A maps to NM_194293.2 G672G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr3:39228920 G>A maps to NM_194293.2 G672G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr3:184100494 C>T maps to NM_003741.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr3:184100494 C>T maps to NM_003741.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr3:194362874 C>T maps to NM_018385.2 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr3:194362874 C>T maps to NM_018385.2 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr4:36230304 C>G maps to NM_015230.2 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr4:36230304 C>G maps to NM_015230.2 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr4:46043202 A>G maps to NM_173536.3 D400D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr4:46043202 A>G maps to NM_173536.3 D400D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr4:55968136 G>A maps to NM_002253.2 D731D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr4:55968136 G>A maps to NM_002253.2 D731D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr4:187531170 T>A did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr4:187531170 T>A did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr5:149677913 G>A maps to NM_001012301.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr5:149677913 G>A maps to NM_001012301.2 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr5:169503007 C>T maps to NM_004946.2 R1596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr5:169503007 C>T maps to NM_004946.2 R1596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr5:179998329 G>A maps to NM_015455.3 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr5:179998329 G>A maps to NM_015455.3 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr6:43230733 C>A maps to NM_032538.1 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr6:43230733 C>A maps to NM_032538.1 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr6:111678328 C>G did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr6:111678328 C>G did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr7:21750197 C>G maps to NM_003777.3 L2244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr7:21750197 C>G maps to NM_003777.3 L2244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr7:100345236 C>G maps to ENST00000349350 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr7:100345236 C>G maps to ENST00000349350 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr7:135292095 C>T maps to NM_015135.2 Q1058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr7:135292095 C>T maps to NM_015135.2 Q1058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr7:150779329 C>T maps to NM_031434.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr7:150779329 C>T maps to NM_031434.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr8:11152789 G>A maps to NM_015458.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr8:11152789 G>A maps to NM_015458.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr8:67808487 C>T maps to NM_173518.4 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr8:67808487 C>T maps to NM_173518.4 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr9:34976156 C>T maps to NM_015297.1 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr9:34976156 C>T maps to NM_015297.1 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr9:88650316 G>A maps to ENST00000376023 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chr9:88650316 G>A maps to ENST00000376023 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chrX:54971912 G>A maps to NM_002625.2 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chrX:54971912 G>A maps to NM_002625.2 R353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chrX:150349839 C>G maps to NM_004224.3 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chrX:150349839 C>G maps to NM_004224.3 T595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr11:12278372 C>T maps to NM_014632.2 S999S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr11:12278372 C>T maps to NM_014632.2 S999S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr12:96288807 G>T maps to NM_182496.2 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr12:96288807 G>T maps to NM_182496.2 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr13:101759892 G>A maps to NM_052867.2 R842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr13:101759892 G>A maps to NM_052867.2 R842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr17:3850834 G>A maps to NM_174953.1 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr17:3850834 G>A maps to NM_174953.1 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr17:7132325 G>A maps to NM_004422.2 D332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr17:7132325 G>A maps to NM_004422.2 D332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr17:7910381 G>A maps to NM_000180.3 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr17:7910381 G>A maps to NM_000180.3 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr2:200298059 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr2:200298059 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr4:96761393 C>T maps to NM_005390.4 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr4:96761393 C>T maps to NM_005390.4 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr6:159653379 G>A maps to NM_032532.2 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr6:159653379 G>A maps to NM_032532.2 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr7:76984646 C>A maps to NM_017439.3 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr7:76984646 C>A maps to NM_017439.3 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr9:104048519 T>A did not map to a codon.
Sequencing variant TCGA-CQ-5329-01A-01D-1683-08 chr9:104048519 T>A did not map to a codon.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr1:118629568 G>A maps to NM_206996.2 D474D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr1:118629568 G>A maps to NM_206996.2 D474D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr11:64521022 C>T maps to NM_005609.2 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr11:64521022 C>T maps to NM_005609.2 A457A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr11:125359381 C>A maps to NM_005103.4 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr11:125359381 C>A maps to NM_005103.4 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr16:47644776 G>A maps to NM_000293.2 Q468Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr16:47644776 G>A maps to NM_000293.2 Q468Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr17:30796050 C>T maps to NM_002815.2 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr17:30796050 C>T maps to NM_002815.2 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr18:7231399 C>T maps to NM_001105581.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr18:7231399 C>T maps to NM_001105581.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr18:51892103 C>T maps to ENST00000382911 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr18:51892103 C>T maps to ENST00000382911 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr19:10791115 G>A maps to NM_017620.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr19:10791115 G>A maps to NM_017620.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr19:46879818 A>G maps to NM_006247.2 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr19:46879818 A>G maps to NM_006247.2 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr19:52619804 C>T maps to NM_178523.3 Q204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr19:52619804 C>T maps to NM_178523.3 Q204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr2:113514029 A>G maps to NM_152515.3 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr2:113514029 A>G maps to NM_152515.3 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr2:220422716 C>T maps to NM_015311.2 W1206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr2:220422716 C>T maps to NM_015311.2 W1206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr2:224749379 C>G maps to NM_020830.3 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr2:224749379 C>G maps to NM_020830.3 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr2:231067412 C>T maps to NM_080424.2 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr2:231067412 C>T maps to NM_080424.2 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr20:44581028 G>A maps to NM_022095.3 C982C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr20:44581028 G>A maps to NM_022095.3 C982C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr4:40440250 C>T maps to NM_001098634.1 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr4:40440250 C>T maps to NM_001098634.1 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr5:98233024 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr5:98233024 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr5:140264048 C>T maps to NM_018904.2 C732C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr5:140264048 C>T maps to NM_018904.2 C732C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr6:127476477 C>T maps to ENST00000368317 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr6:127476477 C>T maps to ENST00000368317 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr8:85799857 G>A maps to NM_001100391.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chr8:85799857 G>A maps to NM_001100391.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chrX:48558588 G>A maps to NM_003173.2 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chrX:48558588 G>A maps to NM_003173.2 K91K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chrX:119388775 A>G maps to NM_001184742.1 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chrX:119388775 A>G maps to NM_001184742.1 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chrX:153696764 C>T maps to NM_017514.3 R1361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5330-01A-01D-1683-08 chrX:153696764 C>T maps to NM_017514.3 R1361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr1:66102650 C>T maps to NM_002303.5 Q1151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr1:66102650 C>T maps to NM_002303.5 Q1151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr1:111778657 C>T maps to NM_004000.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr1:111778657 C>T maps to NM_004000.2 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr1:161254168 G>A maps to NM_001102566.1 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr1:161254168 G>A maps to NM_001102566.1 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr1:228433260 C>G maps to NM_001098623.1 S1210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr1:228433260 C>G maps to NM_001098623.1 S1210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr10:3823968 C>G maps to NM_001300.5 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr10:3823968 C>G maps to NM_001300.5 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr10:70940260 C>T maps to NM_003171.3 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr10:70940260 C>T maps to NM_003171.3 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr11:9456493 C>T maps to NM_006391.2 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr11:9456493 C>T maps to NM_006391.2 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr11:44956497 G>T maps to NM_006034.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr11:44956497 G>T maps to NM_006034.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr12:48545076 C>G maps to NM_024095.3 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr12:48545076 C>G maps to NM_024095.3 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr12:102153833 G>A maps to NM_024312.4 Q1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr12:102153833 G>A maps to NM_024312.4 Q1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr14:23313956 C>T maps to NM_004995.2 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr14:23313956 C>T maps to NM_004995.2 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr15:48500095 C>T maps to NM_000338.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr15:48500095 C>T maps to NM_000338.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr15:50519204 C>T maps to NM_003645.3 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr15:50519204 C>T maps to NM_003645.3 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr16:731285 C>T maps to NM_005861.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr16:731285 C>T maps to NM_005861.2 F98F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr16:20871315 G>C maps to NM_173475.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr16:20871315 G>C maps to NM_173475.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr16:23116890 G>A maps to NM_020718.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr16:23116890 G>A maps to NM_020718.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr17:2234279 G>T maps to NM_018128.4 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr17:2234279 G>T maps to NM_018128.4 I540I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr17:7576926 C>G did not map to a codon.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr17:7576926 C>G did not map to a codon.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr17:56345267 C>T maps to NM_006151.2 F684F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr17:56345267 C>T maps to NM_006151.2 F684F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr17:78444753 C>T maps to NM_002522.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr17:78444753 C>T maps to NM_002522.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr19:22154038 G>C maps to NM_007153.3 S1266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr19:22154038 G>C maps to NM_007153.3 S1266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr19:54724539 G>A maps to NM_001081450.1 Y372Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr19:54724539 G>A maps to NM_001081450.1 Y372Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr2:29240093 G>A maps to NM_199280.2 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr2:29240093 G>A maps to NM_199280.2 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr2:179529383 C>A maps to ENST00000392423 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr2:179529383 C>A maps to ENST00000392423 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr20:24989981 G>C maps to NM_032501.2 S605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr20:24989981 G>C maps to NM_032501.2 S605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr21:43862565 C>G maps to NM_018961.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr21:43862565 C>G maps to NM_018961.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr22:20307264 G>C maps to NM_033257.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr22:20307264 G>C maps to NM_033257.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr22:38698934 G>C maps to NM_001894.4 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr22:38698934 G>C maps to NM_001894.4 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr3:52394092 G>A maps to ENST00000273600 L1523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr3:52394092 G>A maps to ENST00000273600 L1523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr4:337650 G>A maps to NM_003441.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr4:337650 G>A maps to NM_003441.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr5:16067873 A>T maps to NM_001102562.1 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr5:16067873 A>T maps to NM_001102562.1 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr5:64267528 G>C did not map to a codon.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr5:64267528 G>C did not map to a codon.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr5:68715436 C>G maps to NM_001038603.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr5:68715436 C>G maps to NM_001038603.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr5:148427535 G>A maps to NM_024577.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr5:148427535 G>A maps to NM_024577.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr5:178152446 C>T maps to NM_005649.2 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr5:178152446 C>T maps to NM_005649.2 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr6:31779659 G>A maps to NM_005527.3 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr6:31779659 G>A maps to NM_005527.3 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr6:50740384 G>A maps to NM_172238.3 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr6:50740384 G>A maps to NM_172238.3 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr6:52129418 G>T maps to ENST00000419835 V843V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr6:52129418 G>T maps to ENST00000419835 V843V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr6:90660198 G>C maps to NM_001170794.1 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr6:90660198 G>C maps to NM_001170794.1 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr7:63680189 C>G maps to NM_001159524.1 S254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr7:63680189 C>G maps to NM_001159524.1 S254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr7:99474425 G>A maps to NM_001005276.1 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr7:99474425 G>A maps to NM_001005276.1 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr7:100676142 G>A maps to NM_001040105.1 Q482Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr7:100676142 G>A maps to NM_001040105.1 Q482Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr7:138418933 G>A maps to NM_130840.2 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr7:138418933 G>A maps to NM_130840.2 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr8:53570372 T>A maps to NM_014781.4 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr8:53570372 T>A maps to NM_014781.4 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr9:21971028 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr9:21971028 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr9:131084697 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chr9:131084697 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chrX:153735816 G>C maps to ENST00000369641 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5331-01A-02D-1870-08 chrX:153735816 G>C maps to ENST00000369641 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr1:159904571 G>A maps to NM_001135050.1 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr1:159904571 G>A maps to NM_001135050.1 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr1:172555025 T>G maps to ENST00000367723 T684T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr1:172555025 T>G maps to ENST00000367723 T684T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr1:214825108 C>T maps to NM_016343.3 C2680C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr1:214825108 C>T maps to NM_016343.3 C2680C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr1:233394938 G>A maps to NM_014801.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr1:233394938 G>A maps to NM_014801.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr10:115393948 G>A maps to ENST00000369358 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr10:115393948 G>A maps to ENST00000369358 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr10:127438082 C>T maps to ENST00000356792 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr10:127438082 C>T maps to ENST00000356792 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr11:121008283 G>A maps to NM_005422.2 T1032T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr11:121008283 G>A maps to NM_005422.2 T1032T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:30881779 T>C maps to NM_001002259.1 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:30881779 T>C maps to NM_001002259.1 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:40681306 T>C maps to NM_198578.3 S885S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:40681306 T>C maps to NM_198578.3 S885S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:52685195 G>A maps to NM_002281.3 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:52685195 G>A maps to NM_002281.3 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:53849718 C>T maps to NM_005016.5 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:53849718 C>T maps to NM_005016.5 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:54797969 T>A maps to NM_002205.2 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:54797969 T>A maps to NM_002205.2 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:70954685 C>A maps to NM_001109754.1 G1399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:70954685 C>A maps to NM_001109754.1 G1399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:72866929 T>C maps to NM_013381.2 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:72866929 T>C maps to NM_013381.2 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:115109729 C>T maps to NM_016569.3 A716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr12:115109729 C>T maps to NM_016569.3 A716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr13:23915743 G>C maps to NM_014363.4 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr13:23915743 G>C maps to NM_014363.4 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr14:65260352 C>T maps to ENST00000389723 Q680Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr14:65260352 C>T maps to ENST00000389723 Q680Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr15:50211035 C>A maps to NM_024837.2 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr15:50211035 C>A maps to NM_024837.2 E679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr16:424220 C>T maps to NM_021259.2 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr16:424220 C>T maps to NM_021259.2 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr16:8952229 G>A maps to NM_014316.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr16:8952229 G>A maps to NM_014316.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr17:7122261 G>A did not map to a codon.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr17:7122261 G>A did not map to a codon.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr17:10368798 G>A maps to NM_017533.2 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr17:10368798 G>A maps to NM_017533.2 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr17:29253864 C>T maps to ENST00000394782 N88N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr17:29253864 C>T maps to ENST00000394782 N88N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr18:7050889 G>A maps to NM_005559.2 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr18:7050889 G>A maps to NM_005559.2 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr19:37904368 A>T maps to NM_152484.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr19:37904368 A>T maps to NM_152484.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr19:41510325 G>A maps to NM_000767.4 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr19:41510325 G>A maps to NM_000767.4 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr2:106690369 C>T maps to NM_032411.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr2:106690369 C>T maps to NM_032411.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr20:47266016 G>A maps to NM_020820.3 G1042G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr20:47266016 G>A maps to NM_020820.3 G1042G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr20:60485512 C>T maps to NM_001794.2 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr20:60485512 C>T maps to NM_001794.2 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr3:147114185 G>A maps to NM_001168379.1 H85H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr3:147114185 G>A maps to NM_001168379.1 H85H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr3:170716164 A>G maps to NM_000340.1 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr3:170716164 A>G maps to NM_000340.1 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr4:57182511 C>T maps to NM_020722.1 H948H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr4:57182511 C>T maps to NM_020722.1 H948H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr4:82369371 G>A maps to NM_152545.1 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr4:82369371 G>A maps to NM_152545.1 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr5:5319208 C>T maps to NM_139056.2 Y1211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr5:5319208 C>T maps to NM_139056.2 Y1211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr5:59284493 G>A maps to ENST00000502484 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr5:59284493 G>A maps to ENST00000502484 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr5:64946651 G>A maps to NM_001093755.1 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr5:64946651 G>A maps to NM_001093755.1 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr7:4917506 G>A maps to NM_018059.4 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr7:4917506 G>A maps to NM_018059.4 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr7:47342761 G>A maps to NM_022748.11 H1081H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr7:47342761 G>A maps to NM_022748.11 H1081H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr7:73152998 G>A maps to NM_148912.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr7:73152998 G>A maps to NM_148912.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr8:82572901 C>G maps to NM_001144878.1 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr8:82572901 C>G maps to NM_001144878.1 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr9:6460621 C>T maps to NM_152896.1 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr9:6460621 C>T maps to NM_152896.1 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr9:71628057 C>T maps to NM_002732.3 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr9:71628057 C>T maps to NM_002732.3 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr9:130566688 G>T maps to NM_004957.4 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr9:130566688 G>T maps to NM_004957.4 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chrX:50053853 T>G maps to NM_033031.2 S895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chrX:50053853 T>G maps to NM_033031.2 S895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr1:16464346 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr1:16464346 C>A did not map to a codon.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr1:68512776 C>T maps to NM_004675.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr1:68512776 C>T maps to NM_004675.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr1:100387119 C>A maps to ENST00000311030 T1505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr1:100387119 C>A maps to ENST00000311030 T1505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr1:153043108 C>T maps to NM_001017418.1 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr1:153043108 C>T maps to NM_001017418.1 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr1:153520179 G>C maps to NM_002960.1 S95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr1:153520179 G>C maps to NM_002960.1 S95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr10:61112149 C>T maps to ENST00000442566 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr10:61112149 C>T maps to ENST00000442566 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr10:91099030 C>T maps to NM_001549.4 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr10:91099030 C>T maps to NM_001549.4 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr11:7324465 C>T maps to NM_175733.3 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr11:7324465 C>T maps to NM_175733.3 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr11:27389779 G>A maps to NM_018490.2 I830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr11:27389779 G>A maps to NM_018490.2 I830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr11:117161342 C>T maps to NM_012104.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr11:117161342 C>T maps to NM_012104.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr11:118630663 G>A maps to NM_004397.4 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr11:118630663 G>A maps to NM_004397.4 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr12:56334130 G>T maps to NM_201554.1 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr12:56334130 G>T maps to NM_201554.1 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr12:124839419 G>A maps to NM_006312.4 T1156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr12:124839419 G>A maps to NM_006312.4 T1156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr12:130185046 G>A maps to NM_133448.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr12:130185046 G>A maps to NM_133448.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr13:27845675 A>G maps to NM_206827.1 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr13:27845675 A>G maps to NM_206827.1 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr13:32977299 G>A maps to NM_052818.2 R171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr13:32977299 G>A maps to NM_052818.2 R171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr13:109496714 C>T maps to NM_015011.1 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr13:109496714 C>T maps to NM_015011.1 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr14:67850069 G>A maps to NM_004094.4 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr14:67850069 G>A maps to NM_004094.4 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr14:95677034 G>A maps to NM_024734.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr14:95677034 G>A maps to NM_024734.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr14:103802211 C>G maps to NM_183004.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr14:103802211 C>G maps to NM_183004.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr15:23811462 T>G maps to NM_005664.3 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr15:23811462 T>G maps to NM_005664.3 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr15:34395157 G>A maps to NM_152595.4 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr15:34395157 G>A maps to NM_152595.4 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr16:21698870 C>T maps to ENST00000286149 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr16:21698870 C>T maps to ENST00000286149 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr16:50745594 C>T maps to NM_022162.1 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr16:50745594 C>T maps to NM_022162.1 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr16:67650750 G>A maps to NM_006565.3 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr16:67650750 G>A maps to NM_006565.3 K352K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr16:67655478 C>T maps to NM_006565.3 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr16:67655478 C>T maps to NM_006565.3 R448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr16:68405850 C>T maps to NM_018667.3 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr16:68405850 C>T maps to NM_018667.3 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr16:77465452 G>A maps to NM_199355.2 H78H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr16:77465452 G>A maps to NM_199355.2 H78H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr17:7578432 G>C maps to NM_001126112.1 S166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr17:7578432 G>C maps to NM_001126112.1 S166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr17:17248202 C>T maps to ENST00000379552 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr17:17248202 C>T maps to ENST00000379552 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr17:19555869 G>C maps to NM_001031806.1 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr17:19555869 G>C maps to NM_001031806.1 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr17:59999128 T>C maps to NM_020748.2 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr17:59999128 T>C maps to NM_020748.2 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr17:64299052 G>A maps to NM_002737.2 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr17:64299052 G>A maps to NM_002737.2 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr18:909476 C>T maps to NM_001117.3 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr18:909476 C>T maps to NM_001117.3 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr18:5415858 G>A maps to NM_012307.2 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr18:5415858 G>A maps to NM_012307.2 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr18:28923431 C>T maps to NM_001942.2 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr18:28923431 C>T maps to NM_001942.2 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr19:1235905 G>A maps to ENST00000382477 D33D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr19:1235905 G>A maps to ENST00000382477 D33D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr19:5749164 C>T maps to NM_152784.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr19:5749164 C>T maps to NM_152784.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr19:14262301 G>A maps to NM_001008701.2 R1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr19:14262301 G>A maps to NM_001008701.2 R1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr19:39103291 C>A maps to NM_001042600.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr19:39103291 C>A maps to NM_001042600.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr2:223494890 T>G maps to NM_005687.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr2:223494890 T>G maps to NM_005687.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr20:22563765 G>A maps to NM_021784.4 N38N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr20:22563765 G>A maps to NM_021784.4 N38N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr20:37356975 C>T maps to NM_080552.2 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr20:37356975 C>T maps to NM_080552.2 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr20:50158921 C>T maps to NM_012340.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr20:50158921 C>T maps to NM_012340.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr22:29738275 G>A maps to NM_001127.3 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr22:29738275 G>A maps to NM_001127.3 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr22:33733712 C>T maps to NM_133642.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr22:33733712 C>T maps to NM_133642.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr22:50941936 G>A maps to NM_033200.2 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr22:50941936 G>A maps to NM_033200.2 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr3:111732319 A>C maps to NM_001008272.1 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr3:111732319 A>C maps to NM_001008272.1 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr5:140188124 C>T maps to NM_018907.2 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr5:140188124 C>T maps to NM_018907.2 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr5:160059204 G>T maps to NM_025153.2 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr5:160059204 G>T maps to NM_025153.2 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr6:32166456 G>C maps to NM_004557.3 S1529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr6:32166456 G>C maps to NM_004557.3 S1529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr6:43109978 C>T maps to NM_002821.3 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr6:43109978 C>T maps to NM_002821.3 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr6:119245036 G>C maps to ENST00000316316 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr6:119245036 G>C maps to ENST00000316316 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr6:124676414 T>C maps to NM_001040214.1 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr6:124676414 T>C maps to NM_001040214.1 Y65Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr6:146247399 C>T maps to ENST00000367503 L1087L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr6:146247399 C>T maps to ENST00000367503 L1087L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr7:2296547 G>A maps to NM_013321.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr7:2296547 G>A maps to NM_013321.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr7:74114629 C>T maps to NM_032999.2 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr7:74114629 C>T maps to NM_032999.2 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr8:103305963 G>C maps to NM_015902.4 V1486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr8:103305963 G>C maps to NM_015902.4 V1486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr8:143866645 G>A maps to NM_003695.2 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr8:143866645 G>A maps to NM_003695.2 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr8:145661382 C>T maps to NM_013432.4 P811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr8:145661382 C>T maps to NM_013432.4 P811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr9:38396722 C>T maps to NM_000692.3 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr9:38396722 C>T maps to NM_000692.3 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr9:139402561 C>A maps to NM_017617.3 G1119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr9:139402561 C>A maps to NM_017617.3 G1119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chrX:24382303 C>G maps to NM_001136234.1 S476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chrX:24382303 C>G maps to NM_001136234.1 S476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chrX:139586793 G>A maps to NM_005634.2 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chrX:139586793 G>A maps to NM_005634.2 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:12854234 C>T maps to NM_023013.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:12854234 C>T maps to NM_023013.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:16907925 T>A maps to NM_017940.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:16907925 T>A maps to NM_017940.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:26349592 A>G maps to NM_004455.2 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:26349592 A>G maps to NM_004455.2 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:94526179 G>A maps to NM_000350.2 V691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:94526179 G>A maps to NM_000350.2 V691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:160253343 C>T maps to NM_002857.3 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:160253343 C>T maps to NM_002857.3 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:162536138 G>T did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:162536138 G>T did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:172011155 C>T maps to ENST00000359070 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:172011155 C>T maps to ENST00000359070 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:223984131 G>C maps to NM_001031685.2 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr1:223984131 G>C maps to NM_001031685.2 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr10:79737375 C>A maps to NM_007055.3 E1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr10:79737375 C>A maps to NM_007055.3 E1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr10:118969310 C>G maps to NM_181840.1 S219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr10:118969310 C>G maps to NM_181840.1 S219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr11:5444059 C>T maps to NM_001004757.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr11:5444059 C>T maps to NM_001004757.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr11:9321189 A>G maps to NM_015012.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr11:9321189 A>G maps to NM_015012.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr11:44640600 C>A maps to NM_002231.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr11:44640600 C>A maps to NM_002231.3 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr11:64679356 G>A maps to ENST00000421419 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr11:64679356 G>A maps to ENST00000421419 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr11:67925547 G>A maps to NM_017635.3 N755N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr11:67925547 G>A maps to NM_017635.3 N755N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr11:107197636 C>T maps to NM_152434.2 *895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr11:107197636 C>T maps to NM_152434.2 *895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr12:52965208 C>A maps to NM_175053.3 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr12:52965208 C>A maps to NM_175053.3 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr12:131476849 C>T maps to NM_198827.3 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr12:131476849 C>T maps to NM_198827.3 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr12:132323154 A>G did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr12:132323154 A>G did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr13:25744230 C>T maps to NM_152704.2 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr13:25744230 C>T maps to NM_152704.2 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr14:21881156 T>C did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr14:21881156 T>C did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr14:60616103 C>T maps to NM_016029.2 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr14:60616103 C>T maps to NM_016029.2 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr15:69238802 C>G maps to NM_145658.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr15:69238802 C>G maps to NM_145658.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr15:88799154 G>C maps to NM_001012338.1 S77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr15:88799154 G>C maps to NM_001012338.1 S77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr15:90611532 C>T maps to NM_198526.2 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr15:90611532 C>T maps to NM_198526.2 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr16:20371930 G>A maps to NM_174924.1 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr16:20371930 G>A maps to NM_174924.1 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr16:24801450 A>T maps to NM_014494.2 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr16:24801450 A>T maps to NM_014494.2 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr17:10248894 G>A maps to NM_003802.2 Y434Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr17:10248894 G>A maps to NM_003802.2 Y434Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr17:32953440 G>A maps to NM_207313.1 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr17:32953440 G>A maps to NM_207313.1 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr17:62533806 T>C maps to NM_138363.1 D792D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr17:62533806 T>C maps to NM_138363.1 D792D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr17:74001437 G>A maps to NM_001258.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr17:74001437 G>A maps to NM_001258.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr19:52537190 C>A maps to NM_014650.2 E581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr19:52537190 C>A maps to NM_014650.2 E581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr19:55281316 C>T maps to ENST00000291633 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr19:55281316 C>T maps to ENST00000291633 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr2:40366548 G>C maps to NM_021097.2 S846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr2:40366548 G>C maps to NM_021097.2 S846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr2:160243033 G>A maps to NM_013450.2 R1101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr2:160243033 G>A maps to NM_013450.2 R1101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr20:2819569 A>C maps to NM_022760.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr20:2819569 A>C maps to NM_022760.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr20:44422616 C>T maps to NM_052951.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr20:44422616 C>T maps to NM_052951.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr20:62178519 G>A maps to NM_080823.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr20:62178519 G>A maps to NM_080823.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr21:31311809 G>A maps to ENST00000327783 H3H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr21:31311809 G>A maps to ENST00000327783 H3H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr21:47404293 C>G maps to NM_001848.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr21:47404293 C>G maps to NM_001848.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr22:25601218 G>A maps to NM_004076.3 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr22:25601218 G>A maps to NM_004076.3 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr22:50716548 G>A maps to NM_012401.2 V1628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr22:50716548 G>A maps to NM_012401.2 V1628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr3:46008281 G>A maps to NM_024513.2 C848C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr3:46008281 G>A maps to NM_024513.2 C848C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr3:176765337 C>G did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr3:176765337 C>G did not map to a codon.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr4:159753080 C>T maps to ENST00000379346 Y173Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr4:159753080 C>T maps to ENST00000379346 Y173Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr4:187522448 G>A maps to ENST00000260147 R3875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr4:187522448 G>A maps to ENST00000260147 R3875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr5:37303482 G>A maps to NM_153485.1 R1066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr5:37303482 G>A maps to NM_153485.1 R1066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr5:68581235 A>G maps to NM_176816.3 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr5:68581235 A>G maps to NM_176816.3 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr5:140501699 C>T maps to NM_018938.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr5:140501699 C>T maps to NM_018938.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr5:149677007 G>A maps to NM_001012301.2 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr5:149677007 G>A maps to NM_001012301.2 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr6:63989943 G>A maps to NM_016571.2 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr6:63989943 G>A maps to NM_016571.2 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr6:76591500 G>A maps to ENST00000428345 K794K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr6:76591500 G>A maps to ENST00000428345 K794K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr6:90392898 C>T maps to NM_014611.1 L4018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr6:90392898 C>T maps to NM_014611.1 L4018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr6:117246697 C>T maps to NM_173560.3 D587D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr6:117246697 C>T maps to NM_173560.3 D587D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr7:23339006 C>T maps to NM_138446.1 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr7:23339006 C>T maps to NM_138446.1 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr7:48284271 G>A maps to NM_152701.3 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr7:48284271 G>A maps to NM_152701.3 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr8:70585256 G>A maps to NM_030958.2 F798F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr8:70585256 G>A maps to NM_030958.2 F798F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr8:93026817 G>A maps to NM_175634.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr8:93026817 G>A maps to NM_175634.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr8:125094565 C>T maps to NM_001039112.2 L1420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr8:125094565 C>T maps to NM_001039112.2 L1420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr9:5922608 C>T maps to NM_001017969.2 Q1129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr9:5922608 C>T maps to NM_001017969.2 Q1129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr9:121929787 A>T maps to NM_014618.2 R620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr9:121929787 A>T maps to NM_014618.2 R620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr9:140437129 C>T maps to NM_001098537.1 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chr9:140437129 C>T maps to NM_001098537.1 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chrX:23019110 G>T maps to NM_182699.2 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chrX:23019110 G>T maps to NM_182699.2 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chrX:53455529 C>T maps to NM_001031745.1 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chrX:53455529 C>T maps to NM_001031745.1 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chrX:70787354 G>A maps to NM_181672.2 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chrX:70787354 G>A maps to NM_181672.2 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chrX:73960448 C>A maps to NM_001008537.2 E1315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chrX:73960448 C>A maps to NM_001008537.2 E1315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chrX:152159806 A>G maps to NM_001184924.1 D112D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chrX:152159806 A>G maps to NM_001184924.1 D112D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chrX:153706740 G>A maps to NM_006014.3 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6218-01A-11D-1912-08 chrX:153706740 G>A maps to NM_006014.3 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr1:62740511 G>A maps to NM_181712.4 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr1:62740511 G>A maps to NM_181712.4 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr1:152191917 G>A maps to NM_001009931.1 H729H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr1:152191917 G>A maps to NM_001009931.1 H729H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr1:160276271 C>T maps to NM_001098398.1 K438K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr1:160276271 C>T maps to NM_001098398.1 K438K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr10:82264527 C>T maps to NM_030927.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr10:82264527 C>T maps to NM_030927.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr14:50798918 C>G maps to ENST00000358473 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr14:50798918 C>G maps to ENST00000358473 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr16:3724417 G>A maps to NM_016292.2 H322H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr16:3724417 G>A maps to NM_016292.2 H322H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr17:18156754 C>G maps to NM_002018.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr17:18156754 C>G maps to NM_002018.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr17:37571362 G>C maps to NM_004774.3 S472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr17:37571362 G>C maps to NM_004774.3 S472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr18:9257920 A>T maps to NM_015208.3 G1552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr18:9257920 A>T maps to NM_015208.3 G1552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr19:7184589 G>A maps to NM_000208.2 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr19:7184589 G>A maps to NM_000208.2 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr19:13873752 G>C maps to NM_030818.2 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr19:13873752 G>C maps to NM_030818.2 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr2:15374712 C>T maps to NM_015909.2 K2034K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr2:15374712 C>T maps to NM_015909.2 K2034K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr2:18736912 G>A maps to ENST00000444297 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr2:18736912 G>A maps to ENST00000444297 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr2:80085226 T>G maps to ENST00000402739 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr2:80085226 T>G maps to ENST00000402739 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr2:152319684 G>A maps to NM_018151.4 R1217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr2:152319684 G>A maps to NM_018151.4 R1217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr2:155566302 C>T maps to NM_002239.2 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr2:155566302 C>T maps to NM_002239.2 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr2:223066810 C>T maps to NM_181459.3 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr2:223066810 C>T maps to NM_181459.3 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr20:30723920 C>G maps to NM_014742.3 Y58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr20:30723920 C>G maps to NM_014742.3 Y58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr20:33451190 G>A maps to NM_178026.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr20:33451190 G>A maps to NM_178026.2 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr3:154027539 G>A maps to NM_020865.2 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr3:154027539 G>A maps to NM_020865.2 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr3:184025483 G>A maps to NM_002808.3 V762V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr3:184025483 G>A maps to NM_002808.3 V762V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr4:25005705 G>A maps to NM_018176.3 D335D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr4:25005705 G>A maps to NM_018176.3 D335D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr5:145651233 C>T maps to NM_018989.1 F995F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr5:145651233 C>T maps to NM_018989.1 F995F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr6:44217203 C>T maps to NM_007355.2 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr6:44217203 C>T maps to NM_007355.2 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr7:11676025 G>C maps to ENST00000423059 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr7:11676025 G>C maps to ENST00000423059 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr7:140710223 G>C maps to NM_053035.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr7:140710223 G>C maps to NM_053035.2 L70L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CQ-6219-01A-11D-1912-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CQ-6219-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr9:101748162 G>A maps to NM_001855.3 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr9:101748162 G>A maps to NM_001855.3 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chrX:31792156 G>A maps to ENST00000357033 L2488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chrX:31792156 G>A maps to ENST00000357033 L2488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr1:151491339 G>A maps to NM_020770.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr1:151491339 G>A maps to NM_020770.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr1:156450661 G>T maps to NM_005920.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr1:156450661 G>T maps to NM_005920.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr1:160853236 G>A maps to NM_017625.2 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr1:160853236 G>A maps to NM_017625.2 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr1:170695425 C>T maps to NM_022716.2 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr1:170695425 C>T maps to NM_022716.2 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr1:200959777 G>A maps to NM_017596.2 R921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr1:200959777 G>A maps to NM_017596.2 R921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr10:71974335 C>A maps to NM_021129.3 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr10:71974335 C>A maps to NM_021129.3 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr10:95415575 C>T maps to NM_006204.3 F665F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr10:95415575 C>T maps to NM_006204.3 F665F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr10:99130757 G>C maps to NM_015179.3 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr10:99130757 G>C maps to NM_015179.3 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr10:106960921 T>A maps to NM_014978.1 R724R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr10:106960921 T>A maps to NM_014978.1 R724R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr10:116045995 T>C maps to NM_198496.1 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr10:116045995 T>C maps to NM_198496.1 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr11:69933943 C>T maps to NM_018043.5 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr11:69933943 C>T maps to NM_018043.5 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr11:120082136 G>A maps to NM_178507.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr11:120082136 G>A maps to NM_178507.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr12:51382164 C>T maps to NM_001174125.1 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr12:51382164 C>T maps to NM_001174125.1 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr12:123915095 C>T maps to NM_145058.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr12:123915095 C>T maps to NM_145058.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr14:73743878 G>A maps to NM_001005743.1 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr14:73743878 G>A maps to NM_001005743.1 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr14:102506066 G>T maps to NM_001376.4 V3896V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr14:102506066 G>T maps to NM_001376.4 V3896V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr16:1510883 G>A maps to ENST00000382745 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr16:1510883 G>A maps to ENST00000382745 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr16:3063470 C>T maps to NM_020982.3 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr16:3063470 C>T maps to NM_020982.3 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr16:16184308 C>T maps to ENST00000399408 D836D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr16:16184308 C>T maps to ENST00000399408 D836D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr16:20999080 G>C maps to NM_017539.1 V2272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr16:20999080 G>C maps to NM_017539.1 V2272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr17:39881314 C>A maps to ENST00000310778 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr17:39881314 C>A maps to ENST00000310778 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr19:15226687 G>A maps to NM_006844.3 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr19:15226687 G>A maps to NM_006844.3 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr19:17010308 G>A maps to ENST00000443236 R1666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr19:17010308 G>A maps to ENST00000443236 R1666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr19:18232696 G>A maps to NM_015016.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr19:18232696 G>A maps to NM_015016.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr19:51218988 T>A did not map to a codon.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr19:51218988 T>A did not map to a codon.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr2:234637858 A>G maps to NM_019093.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr2:234637858 A>G maps to NM_019093.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr2:234637865 T>C maps to NM_019093.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr2:234637865 T>C maps to NM_019093.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr20:3211606 G>A maps to NM_001174090.1 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr20:3211606 G>A maps to NM_001174090.1 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr20:46386014 C>G maps to NM_001161841.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr20:46386014 C>G maps to NM_001161841.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr22:50687865 C>T maps to NM_032019.5 W194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr22:50687865 C>T maps to NM_032019.5 W194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr3:36872598 T>C maps to NM_014831.2 E2781E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr3:36872598 T>C maps to NM_014831.2 E2781E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr4:155158174 G>A maps to NM_017639.3 N2088N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr4:155158174 G>A maps to NM_017639.3 N2088N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr4:156860669 G>A maps to NM_001334.2 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr4:156860669 G>A maps to NM_001334.2 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr5:52366017 T>C maps to NM_002203.3 N721N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr5:52366017 T>C maps to NM_002203.3 N721N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr5:63257090 G>A maps to NM_000524.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr5:63257090 G>A maps to NM_000524.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr5:149636339 C>T maps to NM_015981.3 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr5:149636339 C>T maps to NM_015981.3 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr6:27839967 G>A maps to NM_003533.2 Y42Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr6:27839967 G>A maps to NM_003533.2 Y42Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr6:126661542 T>C maps to ENST00000368325 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr6:126661542 T>C maps to ENST00000368325 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr6:144416374 C>G maps to NM_031287.2 *87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr6:144416374 C>G maps to NM_031287.2 *87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr7:13950932 C>G did not map to a codon.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr7:13950932 C>G did not map to a codon.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr8:41581096 G>T maps to ENST00000415018 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr8:41581096 G>T maps to ENST00000415018 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr8:140630758 G>A maps to NM_016601.2 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chr8:140630758 G>A maps to NM_016601.2 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chrX:96136645 G>C maps to NM_006729.4 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6220-01A-11D-1912-08 chrX:96136645 G>C maps to NM_006729.4 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr1:906211 G>T maps to ENST00000379409 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr1:906211 G>T maps to ENST00000379409 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr1:7724544 G>C maps to NM_015215.2 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr1:7724544 G>C maps to NM_015215.2 T646T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr1:19992251 C>A maps to NM_000871.1 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr1:19992251 C>A maps to NM_000871.1 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr1:37291331 G>T maps to NM_000831.3 I542I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr1:37291331 G>T maps to NM_000831.3 I542I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr1:89616256 G>A maps to NM_207398.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr1:89616256 G>A maps to NM_207398.2 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr1:109810497 C>G maps to NM_001408.2 S2045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr1:109810497 C>G maps to NM_001408.2 S2045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr1:154306628 C>T maps to NM_020452.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr1:154306628 C>T maps to NM_020452.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr10:28272786 T>A maps to NM_018076.2 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr10:28272786 T>A maps to NM_018076.2 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr10:105207025 G>C maps to NM_015916.4 Y285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr10:105207025 G>C maps to NM_015916.4 Y285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr11:6503306 G>C maps to NM_012192.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr11:6503306 G>C maps to NM_012192.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr11:62292957 C>T maps to NM_001620.1 V2977V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr11:62292957 C>T maps to NM_001620.1 V2977V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr12:49443702 G>C maps to NM_003482.3 S1223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr12:49443702 G>C maps to NM_003482.3 S1223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr12:113442854 C>A maps to NM_016817.2 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr12:113442854 C>A maps to NM_016817.2 V432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr13:32903577 A>C did not map to a codon.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr13:32903577 A>C did not map to a codon.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr13:53419749 C>T maps to NM_002590.2 P883P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr13:53419749 C>T maps to NM_002590.2 P883P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr15:44862785 G>A maps to NM_025137.3 V2138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr15:44862785 G>A maps to NM_025137.3 V2138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr15:58306119 G>C maps to NM_003888.2 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr15:58306119 G>C maps to NM_003888.2 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr15:89169568 G>A maps to NM_022767.3 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr15:89169568 G>A maps to NM_022767.3 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr16:2333283 G>C maps to NM_001089.2 S1313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr16:2333283 G>C maps to NM_001089.2 S1313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr16:20673129 C>T maps to NM_052956.2 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr16:20673129 C>T maps to NM_052956.2 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr17:8017843 G>C maps to ENST00000380149 S369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr17:8017843 G>C maps to ENST00000380149 S369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr17:12655997 C>T maps to NM_001146312.1 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr17:12655997 C>T maps to NM_001146312.1 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr17:19699442 C>T maps to NM_014683.3 Q654Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr17:19699442 C>T maps to NM_014683.3 Q654Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr17:27228112 C>A maps to NM_144683.3 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr17:27228112 C>A maps to NM_144683.3 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr17:78184559 C>T maps to NM_000199.3 Q400Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr17:78184559 C>T maps to NM_000199.3 Q400Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr19:15355573 C>T did not map to a codon.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr19:15355573 C>T did not map to a codon.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr19:37117053 T>C maps to NM_032825.3 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr19:37117053 T>C maps to NM_032825.3 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr2:30143410 G>A maps to NM_004304.3 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr2:30143410 G>A maps to NM_004304.3 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr2:37310506 G>A maps to NM_019024.1 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr2:37310506 G>A maps to NM_019024.1 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr2:242441063 C>T maps to NM_006374.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr2:242441063 C>T maps to NM_006374.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr21:43258050 C>T maps to NM_022115.3 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr21:43258050 C>T maps to NM_022115.3 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr4:2717748 G>C did not map to a codon.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr4:2717748 G>C did not map to a codon.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr4:70360952 C>T maps to NM_021139.2 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr4:70360952 C>T maps to NM_021139.2 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr4:71509482 G>A maps to NM_031889.2 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr4:71509482 G>A maps to NM_031889.2 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr5:132427045 C>T maps to NM_002154.3 Q514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr5:132427045 C>T maps to NM_002154.3 Q514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr6:111680070 G>A maps to NM_002912.3 L2342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr6:111680070 G>A maps to NM_002912.3 L2342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr8:81897256 C>G maps to NM_018440.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr8:81897256 C>G maps to NM_018440.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr8:103301698 A>T maps to NM_015902.4 V1565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chr8:103301698 A>T maps to NM_015902.4 V1565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chrX:107084608 A>G maps to NM_012216.3 K238K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6221-01A-11D-2078-08 chrX:107084608 A>G maps to NM_012216.3 K238K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr1:210857105 G>A maps to NM_172362.2 G829G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr1:210857105 G>A maps to NM_172362.2 G829G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr10:22898586 G>A maps to NM_005028.4 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr10:22898586 G>A maps to NM_005028.4 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr10:73521631 G>T maps to NM_022153.1 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr10:73521631 G>T maps to NM_022153.1 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr10:104164345 G>C maps to NM_002779.3 L898L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr10:104164345 G>C maps to NM_002779.3 L898L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr11:46898165 G>A maps to ENST00000256991 L1174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr11:46898165 G>A maps to ENST00000256991 L1174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr12:109194620 G>A maps to NM_018984.3 Y361Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr12:109194620 G>A maps to NM_018984.3 Y361Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr13:25265210 G>A maps to NM_001185085.1 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr13:25265210 G>A maps to NM_001185085.1 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr16:16205305 C>T maps to ENST00000399408 F992F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr16:16205305 C>T maps to ENST00000399408 F992F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr16:87678467 G>A maps to NM_020655.2 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr16:87678467 G>A maps to NM_020655.2 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr18:48581280 C>G maps to NM_005359.5 Y195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr18:48581280 C>G maps to NM_005359.5 Y195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr19:35435247 G>T maps to NM_001099438.1 E461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr19:35435247 G>T maps to NM_001099438.1 E461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr2:119726796 G>A maps to NM_006770.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr2:119726796 G>A maps to NM_006770.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr2:211179748 G>A maps to NM_079420.2 D6D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr2:211179748 G>A maps to NM_079420.2 D6D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr4:187560904 G>A maps to ENST00000260147 R1205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr4:187560904 G>A maps to ENST00000260147 R1205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr5:50057653 G>T did not map to a codon.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr5:50057653 G>T did not map to a codon.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr6:26056551 C>T maps to NM_005319.3 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr6:26056551 C>T maps to NM_005319.3 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr6:153073383 G>A maps to NM_003381.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr6:153073383 G>A maps to NM_003381.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr6:168352491 G>A maps to ENST00000400822 R1478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr6:168352491 G>A maps to ENST00000400822 R1478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr7:22190087 G>A maps to ENST00000344041 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr7:22190087 G>A maps to ENST00000344041 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr7:44151907 G>A maps to NM_001129.3 S735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr7:44151907 G>A maps to NM_001129.3 S735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr7:94539550 A>G maps to NM_001166160.1 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr7:94539550 A>G maps to NM_001166160.1 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr8:21857169 G>T maps to ENST00000434536 G932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr8:21857169 G>T maps to ENST00000434536 G932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr9:113563103 C>T maps to ENST00000189978 R822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6222-01A-11D-1912-08 chr9:113563103 C>T maps to ENST00000189978 R822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr1:32154662 G>T maps to NM_001856.3 I548I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr1:32154662 G>T maps to NM_001856.3 I548I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr1:228437859 C>T maps to NM_001098623.1 Q1410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr1:228437859 C>T maps to NM_001098623.1 Q1410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr1:247588448 C>T maps to NM_004895.4 F568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr1:247588448 C>T maps to NM_004895.4 F568F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr10:51464880 G>A maps to ENST00000416142 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr10:51464880 G>A maps to ENST00000416142 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr11:123993787 C>T maps to NM_014622.4 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr11:123993787 C>T maps to NM_014622.4 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr12:33559822 T>C maps to NM_198992.3 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr12:33559822 T>C maps to NM_198992.3 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr12:48543325 C>T maps to NM_024095.3 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr12:48543325 C>T maps to NM_024095.3 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr12:109634898 G>A maps to NM_001093.3 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr12:109634898 G>A maps to NM_001093.3 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr12:130912861 G>A maps to NM_015347.4 D741D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr12:130912861 G>A maps to NM_015347.4 D741D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr13:39265020 C>T maps to NM_207361.4 P1180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr13:39265020 C>T maps to NM_207361.4 P1180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr13:61986230 G>A maps to NM_022843.3 D667D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr13:61986230 G>A maps to NM_022843.3 D667D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr13:70456524 C>A maps to NM_020866.2 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr13:70456524 C>A maps to NM_020866.2 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr14:104206646 G>C maps to NM_015316.2 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr14:104206646 G>C maps to NM_015316.2 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr15:42437771 C>A did not map to a codon.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr15:42437771 C>A did not map to a codon.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr15:89169643 C>T maps to NM_022767.3 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr15:89169643 C>T maps to NM_022767.3 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr16:58202513 C>T maps to NM_001896.2 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr16:58202513 C>T maps to NM_001896.2 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr16:88643836 C>T maps to ENST00000452588 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr16:88643836 C>T maps to ENST00000452588 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr19:18329001 G>A maps to NM_000923.3 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr19:18329001 G>A maps to NM_000923.3 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr19:36217141 T>C maps to NM_014727.1 C1297C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr19:36217141 T>C maps to NM_014727.1 C1297C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr19:55824406 G>T maps to NM_001085488.1 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr19:55824406 G>T maps to NM_001085488.1 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr19:55824418 G>A maps to NM_001085488.1 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr19:55824418 G>A maps to NM_001085488.1 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr2:25469958 C>T maps to NM_175629.1 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr2:25469958 C>T maps to NM_175629.1 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr3:128993712 C>T maps to NM_016128.3 H763H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr3:128993712 C>T maps to NM_016128.3 H763H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr4:80993705 C>T maps to NM_001145794.1 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr4:80993705 C>T maps to NM_001145794.1 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr4:187584692 G>A maps to ENST00000260147 Q1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr4:187584692 G>A maps to ENST00000260147 Q1114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr5:140784240 T>C maps to NM_018921.2 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr5:140784240 T>C maps to NM_018921.2 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr5:148899952 T>C did not map to a codon.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr5:148899952 T>C did not map to a codon.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr5:169474560 C>A maps to NM_004946.2 P1338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr5:169474560 C>A maps to NM_004946.2 P1338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr5:171809083 C>A maps to NM_001017995.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr5:171809083 C>A maps to NM_001017995.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr6:30029435 C>A maps to NM_170783.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr6:30029435 C>A maps to NM_170783.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr6:111583599 C>A maps to NM_153369.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr6:111583599 C>A maps to NM_153369.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr7:97821069 G>A maps to NM_014916.3 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr7:97821069 G>A maps to NM_014916.3 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr8:39624563 T>C did not map to a codon.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chr8:39624563 T>C did not map to a codon.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chrX:16168685 G>A maps to NM_005314.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chrX:16168685 G>A maps to NM_005314.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chrX:129479182 G>T maps to ENST00000339231 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6223-01A-11D-1912-08 chrX:129479182 G>T maps to ENST00000339231 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr1:29508252 C>T maps to NM_005626.4 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr1:29508252 C>T maps to NM_005626.4 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr1:186106020 C>T maps to NM_031935.2 R4512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr1:186106020 C>T maps to NM_031935.2 R4512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr1:228468012 C>T maps to NM_001098623.1 N2599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr1:228468012 C>T maps to NM_001098623.1 N2599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr11:68658834 C>T maps to NM_181514.1 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr11:68658834 C>T maps to NM_181514.1 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr11:130078331 C>T maps to NM_021978.3 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr11:130078331 C>T maps to NM_021978.3 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr16:54966558 C>T maps to NM_005853.5 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr16:54966558 C>T maps to NM_005853.5 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr16:67700076 G>A maps to NM_032140.1 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr16:67700076 G>A maps to NM_032140.1 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr17:40322230 C>T maps to NM_012285.2 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr17:40322230 C>T maps to NM_012285.2 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr17:56232954 C>T maps to NM_012374.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr17:56232954 C>T maps to NM_012374.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr17:79866788 G>A maps to NM_001184917.1 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr17:79866788 G>A maps to NM_001184917.1 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr19:14070878 C>T maps to NM_138353.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr19:14070878 C>T maps to NM_138353.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr19:14517887 G>A maps to NM_078481.2 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr19:14517887 G>A maps to NM_078481.2 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr19:50357787 C>T maps to NM_017432.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr19:50357787 C>T maps to NM_017432.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr19:55889197 G>A maps to NM_139172.1 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr19:55889197 G>A maps to NM_139172.1 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr2:182542609 G>A maps to NM_002500.2 C326C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr2:182542609 G>A maps to NM_002500.2 C326C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr2:234669124 C>T maps to NM_000463.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr2:234669124 C>T maps to NM_000463.2 A64A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CQ-6224-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr20:34022564 C>T maps to ENST00000374375 T203T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CQ-6224-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr20:34022564 C>T maps to ENST00000374375 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr3:170198807 C>T maps to NM_020949.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr3:170198807 C>T maps to NM_020949.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr4:187172683 A>G maps to ENST00000511608 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr4:187172683 A>G maps to ENST00000511608 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr5:139201498 G>A maps to NM_032289.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr5:139201498 G>A maps to NM_032289.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr5:148590345 G>A maps to NM_014945.2 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr5:148590345 G>A maps to NM_014945.2 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr6:22294766 G>A maps to ENST00000397199 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr6:22294766 G>A maps to ENST00000397199 S26S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CQ-6224-01A-11D-1912-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CQ-6224-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr7:104377218 T>C maps to NM_199000.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr7:104377218 T>C maps to NM_199000.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr7:110764282 C>T maps to NM_018334.4 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr7:110764282 C>T maps to NM_018334.4 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr8:28573797 C>T maps to NM_001440.2 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr8:28573797 C>T maps to NM_001440.2 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr8:144392335 C>T maps to NM_052963.1 A535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr8:144392335 C>T maps to NM_052963.1 A535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr8:145154028 G>A maps to NM_030974.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr8:145154028 G>A maps to NM_030974.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr8:145584282 G>A maps to NM_024531.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr8:145584282 G>A maps to NM_024531.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr9:73002723 G>A maps to NM_001206.2 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr9:73002723 G>A maps to NM_001206.2 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chrX:41077798 G>A maps to NM_001039590.2 L2128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chrX:41077798 G>A maps to NM_001039590.2 L2128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr1:45293265 G>A maps to NM_003738.4 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr1:45293265 G>A maps to NM_003738.4 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr1:156233236 G>C maps to NM_015327.2 V660V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr1:156233236 G>C maps to NM_015327.2 V660V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr1:200956236 G>A maps to NM_017596.2 S1167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr1:200956236 G>A maps to NM_017596.2 S1167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr10:73405727 C>T maps to ENST00000398860 Y432Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr10:73405727 C>T maps to ENST00000398860 Y432Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr11:113712436 A>G maps to NM_020886.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr11:113712436 A>G maps to NM_020886.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr12:21325612 T>C maps to NM_006446.4 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr12:21325612 T>C maps to NM_006446.4 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr12:31820645 C>T maps to NM_001135864.1 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr12:31820645 C>T maps to NM_001135864.1 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr12:49448534 C>T did not map to a codon.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr12:49448534 C>T did not map to a codon.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr12:125397971 G>A maps to NM_021009.5 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr12:125397971 G>A maps to NM_021009.5 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr14:55878477 C>A maps to NM_014924.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr14:55878477 C>A maps to NM_014924.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr15:28413736 C>G did not map to a codon.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr15:28413736 C>G did not map to a codon.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr15:31354780 C>G did not map to a codon.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr15:31354780 C>G did not map to a codon.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr15:48500014 T>C maps to NM_000338.2 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr15:48500014 T>C maps to NM_000338.2 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr15:54305277 A>T maps to ENST00000260323 K60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr15:54305277 A>T maps to ENST00000260323 K60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr15:56386607 A>C maps to NM_022841.5 S1106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr15:56386607 A>C maps to NM_022841.5 S1106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr16:23382770 C>T maps to ENST00000307331 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr16:23382770 C>T maps to ENST00000307331 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr16:24990292 T>C maps to NM_001006634.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr16:24990292 T>C maps to NM_001006634.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr16:57290896 G>A maps to NM_015993.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr16:57290896 G>A maps to NM_015993.2 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr17:8172073 C>T maps to NM_012393.2 Y1202Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr17:8172073 C>T maps to NM_012393.2 Y1202Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr17:49074036 G>T maps to ENST00000376407 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr17:49074036 G>T maps to ENST00000376407 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr17:58967053 A>G did not map to a codon.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr17:58967053 A>G did not map to a codon.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr17:76212843 A>G maps to NM_001012271.1 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr17:76212843 A>G maps to NM_001012271.1 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr18:13737129 T>A maps to NM_003799.1 C225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr18:13737129 T>A maps to NM_003799.1 C225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr19:13411467 G>A maps to NM_023035.2 D729D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr19:13411467 G>A maps to NM_023035.2 D729D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr19:30936463 C>T maps to NM_014717.1 H665H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr19:30936463 C>T maps to NM_014717.1 H665H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr19:37118396 C>G maps to NM_032825.3 S533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr19:37118396 C>G maps to NM_032825.3 S533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr19:44933284 G>T maps to NM_014518.2 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr19:44933284 G>T maps to NM_014518.2 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr19:50906793 C>G maps to ENST00000391817 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr19:50906793 C>G maps to ENST00000391817 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr2:71780157 C>G maps to NM_001130987.1 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr2:71780157 C>G maps to NM_001130987.1 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr2:158162304 T>C maps to NM_014568.1 T828T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr2:158162304 T>C maps to NM_014568.1 T828T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr2:163280004 A>T maps to NM_033272.2 I665I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr2:163280004 A>T maps to NM_033272.2 I665I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr2:185803539 C>G maps to NM_194250.1 T1139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr2:185803539 C>G maps to NM_194250.1 T1139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr2:209308081 T>C maps to NM_005048.2 H173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr2:209308081 T>C maps to NM_005048.2 H173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr20:408137 T>C did not map to a codon.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr20:408137 T>C did not map to a codon.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr20:1559071 G>C maps to NM_006065.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr20:1559071 G>C maps to NM_006065.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr20:36012654 C>T maps to ENST00000373558 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr20:36012654 C>T maps to ENST00000373558 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr3:100275787 A>G maps to ENST00000403410 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr3:100275787 A>G maps to ENST00000403410 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr3:142740398 T>C did not map to a codon.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr3:142740398 T>C did not map to a codon.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr3:151597695 G>A did not map to a codon.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr3:151597695 G>A did not map to a codon.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr4:39290413 G>A maps to ENST00000381897 P1138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr4:39290413 G>A maps to ENST00000381897 P1138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr4:65175549 C>T maps to NM_001010874.4 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr4:65175549 C>T maps to NM_001010874.4 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr5:23526666 A>T maps to NM_020227.2 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr5:23526666 A>T maps to NM_020227.2 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr5:177574773 C>T maps to NM_022762.3 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr5:177574773 C>T maps to NM_022762.3 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr6:46658978 C>T maps to NM_001010870.2 T1038T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr6:46658978 C>T maps to NM_001010870.2 T1038T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr6:97694536 T>C maps to NM_198468.2 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr6:97694536 T>C maps to NM_198468.2 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr6:110301052 G>A maps to ENST00000414000 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr6:110301052 G>A maps to ENST00000414000 V261V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CQ-6225-01A-11D-1912-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CQ-6225-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr7:99565808 C>A maps to NM_001185.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr7:99565808 C>A maps to NM_001185.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr7:103143678 T>A did not map to a codon.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr7:103143678 T>A did not map to a codon.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr7:139258059 C>T maps to NM_022740.4 P1070P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr7:139258059 C>T maps to NM_022740.4 P1070P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr7:148947392 G>A maps to NM_012256.3 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr7:148947392 G>A maps to NM_012256.3 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr7:154862704 C>T maps to NM_024012.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr7:154862704 C>T maps to NM_024012.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr8:8185977 C>G did not map to a codon.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr8:8185977 C>G did not map to a codon.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr8:30557644 G>A maps to NM_000637.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr8:30557644 G>A maps to NM_000637.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr8:52773447 T>C maps to NM_052937.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr8:52773447 T>C maps to NM_052937.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr8:106815639 T>C maps to NM_012082.3 G1110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6225-01A-11D-1912-08 chr8:106815639 T>C maps to NM_012082.3 G1110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr1:6699996 C>G maps to NM_018198.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr1:6699996 C>G maps to NM_018198.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr11:72145269 G>T maps to NM_030813.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr11:72145269 G>T maps to NM_030813.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr11:74904299 C>T maps to NM_007256.4 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr11:74904299 C>T maps to NM_007256.4 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr12:13061573 C>T maps to NM_003979.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr12:13061573 C>T maps to NM_003979.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr14:23609753 G>A maps to NM_012244.2 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr14:23609753 G>A maps to NM_012244.2 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr15:51741320 G>A maps to NM_001174116.1 R2992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr15:51741320 G>A maps to NM_001174116.1 R2992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr16:84520477 G>T maps to NM_020947.3 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr16:84520477 G>T maps to NM_020947.3 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr17:74006564 A>G maps to NM_001988.2 P907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr17:74006564 A>G maps to NM_001988.2 P907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr19:17918901 C>T maps to NM_014256.3 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr19:17918901 C>T maps to NM_014256.3 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr19:37440778 C>T maps to NM_198539.2 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr19:37440778 C>T maps to NM_198539.2 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr19:50385366 C>T maps to NM_024682.2 H199H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr19:50385366 C>T maps to NM_024682.2 H199H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr19:57931030 G>A maps to NM_006959.2 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr19:57931030 G>A maps to NM_006959.2 E57E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr2:38302532 C>T did not map to a codon.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr2:38302532 C>T did not map to a codon.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr21:30934005 G>T maps to ENST00000327783 C765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr21:30934005 G>T maps to ENST00000327783 C765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr21:42754439 C>T maps to NM_002463.1 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr21:42754439 C>T maps to NM_002463.1 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr3:51978491 C>A maps to NM_001003931.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr3:51978491 C>A maps to NM_001003931.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr3:165547360 G>A maps to NM_000055.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr3:165547360 G>A maps to NM_000055.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr6:27860846 A>G maps to NM_003514.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6227-01A-11D-1912-08 chr6:27860846 A>G maps to NM_003514.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr1:109801081 C>T maps to NM_001408.2 C1113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr1:109801081 C>T maps to NM_001408.2 C1113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr1:156510538 G>T maps to NM_178229.4 I900I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr1:156510538 G>T maps to NM_178229.4 I900I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr1:204226791 G>A maps to ENST00000367191 Q425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr1:204226791 G>A maps to ENST00000367191 Q425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr10:89118156 T>C maps to ENST00000330762 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr10:89118156 T>C maps to ENST00000330762 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr11:639779 G>A maps to NM_000797.3 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr11:639779 G>A maps to NM_000797.3 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr12:6788349 C>G did not map to a codon.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr12:6788349 C>G did not map to a codon.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr12:38714761 C>G maps to NM_001013620.3 S390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr12:38714761 C>G maps to NM_001013620.3 S390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr12:95442957 G>A maps to NM_003297.2 C339C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr12:95442957 G>A maps to NM_003297.2 C339C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr12:97337516 G>T maps to NM_001135175.1 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr12:97337516 G>T maps to NM_001135175.1 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr15:83796129 T>C maps to NM_023003.3 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr15:83796129 T>C maps to NM_023003.3 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr16:29814095 A>G maps to NM_007317.1 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr16:29814095 A>G maps to NM_007317.1 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr16:50707786 G>A maps to NM_182854.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr16:50707786 G>A maps to NM_182854.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr16:67670699 A>T maps to NM_006565.3 K649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr16:67670699 A>T maps to NM_006565.3 K649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr17:7579385 T>A maps to NM_001126112.1 K101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr17:7579385 T>A maps to NM_001126112.1 K101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr19:10204169 G>A maps to NM_031917.2 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr19:10204169 G>A maps to NM_031917.2 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr19:18675831 G>A did not map to a codon.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr19:18675831 G>A did not map to a codon.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr2:71629114 C>G maps to NM_014497.3 V909V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr2:71629114 C>G maps to NM_014497.3 V909V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr2:71901426 G>A did not map to a codon.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr2:71901426 G>A did not map to a codon.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr2:219543896 C>T maps to NM_015690.3 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr2:219543896 C>T maps to NM_015690.3 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr2:234460154 A>C maps to NM_018218.2 L247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr2:234460154 A>C maps to NM_018218.2 L247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr21:30934038 G>T maps to ENST00000327783 S754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr21:30934038 G>T maps to ENST00000327783 S754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr3:9807480 C>T maps to NM_003656.3 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr3:9807480 C>T maps to NM_003656.3 K59K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr3:132185173 C>G maps to NM_015268.3 S667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr3:132185173 C>G maps to NM_015268.3 S667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr6:26158374 G>A did not map to a codon.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr6:26158374 G>A did not map to a codon.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr6:121615731 T>C maps to ENST00000275159 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr6:121615731 T>C maps to ENST00000275159 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr7:39472770 G>A maps to NM_007252.3 Q374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr7:39472770 G>A maps to NM_007252.3 Q374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr7:44578579 G>A maps to NM_013389.2 Y472Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr7:44578579 G>A maps to NM_013389.2 Y472Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr7:73480042 C>T maps to ENST00000358929 A739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr7:73480042 C>T maps to ENST00000358929 A739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr7:107880401 C>T did not map to a codon.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr7:107880401 C>T did not map to a codon.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr8:67039640 G>T maps to NM_184085.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr8:67039640 G>T maps to NM_184085.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chrX:30326946 C>T maps to NM_000475.4 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chrX:30326946 C>T maps to NM_000475.4 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chrX:101912581 T>C maps to NM_001184727.1 Y1247Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chrX:101912581 T>C maps to NM_001184727.1 Y1247Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr1:175334301 T>G maps to NM_003285.2 R811R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr1:175334301 T>G maps to NM_003285.2 R811R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr11:68548197 C>T maps to NM_001876.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr11:68548197 C>T maps to NM_001876.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr15:85165177 G>A maps to NM_181877.3 K584K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr15:85165177 G>A maps to NM_181877.3 K584K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr15:93015668 G>A maps to NM_153040.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr15:93015668 G>A maps to NM_153040.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr6:31928455 A>G maps to NM_006929.4 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr6:31928455 A>G maps to NM_006929.4 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr6:31931704 C>T maps to NM_006929.4 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr6:31931704 C>T maps to NM_006929.4 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr7:48390324 C>T maps to NM_152701.3 C3430C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr7:48390324 C>T maps to NM_152701.3 C3430C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr7:84651710 T>G maps to NM_152754.2 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr7:84651710 T>G maps to NM_152754.2 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr8:642490 C>G maps to NM_207332.1 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr8:642490 C>G maps to NM_207332.1 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr8:92988160 G>A maps to NM_175634.2 Y440Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6229-01A-11D-1912-08 chr8:92988160 G>A maps to NM_175634.2 Y440Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr11:128710111 G>A maps to NM_000220.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr11:128710111 G>A maps to NM_000220.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr12:57871046 A>T maps to ENST00000393797 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr12:57871046 A>T maps to ENST00000393797 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr12:123200126 G>A maps to NM_006018.2 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr12:123200126 G>A maps to NM_006018.2 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr14:20216209 T>C maps to NM_172194.1 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr14:20216209 T>C maps to NM_172194.1 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr19:9085092 G>T maps to NM_024690.2 S2241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr19:9085092 G>T maps to NM_024690.2 S2241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr2:217543683 C>T maps to NM_000599.3 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr2:217543683 C>T maps to NM_000599.3 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr4:177136849 G>A maps to NM_080874.3 C297C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr4:177136849 G>A maps to NM_080874.3 C297C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr5:113829156 G>A maps to NM_021614.2 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr5:113829156 G>A maps to NM_021614.2 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr5:122725741 C>T maps to NM_153223.3 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr5:122725741 C>T maps to NM_153223.3 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr5:140189039 G>A maps to NM_018907.2 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr5:140189039 G>A maps to NM_018907.2 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr5:140255407 C>T maps to NM_018903.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr5:140255407 C>T maps to NM_018903.2 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr8:87917338 C>T maps to NM_173538.2 H63H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chr8:87917338 C>T maps to NM_173538.2 H63H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chrX:140994878 C>G maps to NM_005462.4 Y563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7065-01A-11D-2078-08 chrX:140994878 C>G maps to NM_005462.4 Y563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr1:237947221 G>A maps to NM_001035.2 A4070A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr1:237947221 G>A maps to NM_001035.2 A4070A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr12:21196319 T>C maps to ENST00000381541 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr12:21196319 T>C maps to ENST00000381541 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr15:34434541 A>C maps to NM_024713.2 *305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr15:34434541 A>C maps to NM_024713.2 *305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr15:48056382 T>C maps to NM_153618.1 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr15:48056382 T>C maps to NM_153618.1 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr16:31193978 C>T maps to NM_004960.3 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr16:31193978 C>T maps to NM_004960.3 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr17:7576851 C>T did not map to a codon.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr17:7576851 C>T did not map to a codon.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr17:33806811 C>T maps to ENST00000361112 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr17:33806811 C>T maps to ENST00000361112 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr17:36104707 G>A maps to NM_000458.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr17:36104707 G>A maps to NM_000458.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr17:37814248 A>G maps to NM_006804.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr17:37814248 A>G maps to NM_006804.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr4:87731007 T>C maps to NM_080685.2 T2395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr4:87731007 T>C maps to NM_080685.2 T2395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr5:2748945 C>T maps to NM_033267.4 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr5:2748945 C>T maps to NM_033267.4 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr7:42262780 G>A maps to NM_000168.5 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr7:42262780 G>A maps to NM_000168.5 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr7:87051438 G>A maps to NM_018849.2 Q772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr7:87051438 G>A maps to NM_018849.2 Q772*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr8:12952313 T>A maps to NM_182643.2 P1160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr8:12952313 T>A maps to NM_182643.2 P1160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr9:85615350 G>A maps to NM_152573.2 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr9:85615350 G>A maps to NM_152573.2 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr9:136518096 A>G maps to NM_000787.3 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr9:136518096 A>G maps to NM_000787.3 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chrX:53105970 T>A maps to NM_018969.5 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chrX:53105970 T>A maps to NM_018969.5 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chrX:57337037 G>A maps to NM_174912.3 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chrX:57337037 G>A maps to NM_174912.3 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr1:32207756 C>T maps to NM_001703.2 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr1:32207756 C>T maps to NM_001703.2 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr1:151688427 C>G maps to NM_007185.4 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr1:151688427 C>G maps to NM_007185.4 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr1:159162469 C>G maps to NM_021189.3 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr1:159162469 C>G maps to NM_021189.3 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr1:203467830 C>T maps to NM_014359.3 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr1:203467830 C>T maps to NM_014359.3 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr11:5462198 G>C maps to NM_001005288.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr11:5462198 G>C maps to NM_001005288.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr11:6816909 C>G maps to NM_003696.2 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr11:6816909 C>G maps to NM_003696.2 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr11:17428293 C>T maps to ENST00000302539 T1069T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr11:17428293 C>T maps to ENST00000302539 T1069T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr11:113934864 G>T maps to NM_001018011.1 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr11:113934864 G>T maps to NM_001018011.1 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr12:112602001 G>A maps to NM_001109662.2 S4032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr12:112602001 G>A maps to NM_001109662.2 S4032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr12:117595802 C>A maps to NM_033624.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr12:117595802 C>A maps to NM_033624.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr13:25266964 A>G maps to NM_001185085.1 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr13:25266964 A>G maps to NM_001185085.1 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr13:84453668 C>T maps to NM_052910.1 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr13:84453668 C>T maps to NM_052910.1 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr13:88329805 C>T maps to NM_015567.1 G721G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr13:88329805 C>T maps to NM_015567.1 G721G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr14:57857725 T>G maps to NM_001011713.2 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr14:57857725 T>G maps to NM_001011713.2 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr14:92628078 C>T maps to NM_017437.1 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr14:92628078 C>T maps to NM_017437.1 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr16:65006888 C>T maps to NM_001797.2 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr16:65006888 C>T maps to NM_001797.2 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr17:79073792 C>T maps to NM_017451.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr17:79073792 C>T maps to NM_017451.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr18:56620895 G>A maps to NM_018181.4 K1005K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr18:56620895 G>A maps to NM_018181.4 K1005K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr19:9204510 C>T maps to ENST00000305465 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr19:9204510 C>T maps to ENST00000305465 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr19:41726661 G>A maps to NM_021913.3 W69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr19:41726661 G>A maps to NM_021913.3 W69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr19:49132291 G>A maps to NM_020126.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr19:49132291 G>A maps to NM_020126.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr2:21233457 G>A maps to NM_000384.2 N2094N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr2:21233457 G>A maps to NM_000384.2 N2094N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr2:111419370 C>T maps to NM_004336.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr2:111419370 C>T maps to NM_004336.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr2:128262664 G>A maps to NM_017969.2 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr2:128262664 G>A maps to NM_017969.2 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr2:220439821 T>C maps to NM_002191.3 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr2:220439821 T>C maps to NM_002191.3 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr3:128181437 C>T maps to NM_153330.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr3:128181437 C>T maps to NM_153330.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr4:7795474 G>A maps to NM_001134647.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr4:7795474 G>A maps to NM_001134647.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr5:150723749 G>A maps to NM_181776.2 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr5:150723749 G>A maps to NM_181776.2 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr6:42224468 C>T maps to NM_033502.2 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr6:42224468 C>T maps to NM_033502.2 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr6:72889448 C>T maps to NM_014989.4 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr6:72889448 C>T maps to NM_014989.4 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr6:107390675 G>A maps to NM_001080450.2 F573F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr6:107390675 G>A maps to NM_001080450.2 F573F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr6:136687110 C>T maps to NM_001198609.1 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr6:136687110 C>T maps to NM_001198609.1 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr7:155599119 G>A maps to NM_000193.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr7:155599119 G>A maps to NM_000193.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr8:119123159 A>T maps to NM_000127.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr8:119123159 A>T maps to NM_000127.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr8:141370155 C>G maps to NM_031466.5 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr8:141370155 C>G maps to NM_031466.5 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr8:144992792 G>A maps to NM_201380.2 F3869F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr8:144992792 G>A maps to NM_201380.2 F3869F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr9:97369180 A>G maps to NM_001127628.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr9:97369180 A>G maps to NM_001127628.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr9:139912244 G>C maps to ENST00000355090 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chr9:139912244 G>C maps to ENST00000355090 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chrX:37026575 G>A maps to NM_001013736.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chrX:37026575 G>A maps to NM_001013736.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chrX:152813446 C>T maps to NM_001001344.2 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-7068-01A-11D-2078-08 chrX:152813446 C>T maps to NM_001001344.2 I371I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr1:46745879 C>T maps to ENST00000254454 Q646Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr1:46745879 C>T maps to ENST00000254454 Q646Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr1:151804260 G>A did not map to a codon.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr1:151804260 G>A did not map to a codon.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr1:156255559 G>A maps to NM_032323.2 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr1:156255559 G>A maps to NM_032323.2 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr1:243727051 G>A maps to NM_005465.3 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr1:243727051 G>A maps to NM_005465.3 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr10:103867954 G>A maps to NM_001113407.1 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr10:103867954 G>A maps to NM_001113407.1 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr12:52307463 G>A maps to NM_001077401.1 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr12:52307463 G>A maps to NM_001077401.1 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr13:113530143 C>T maps to NM_032189.3 S1072S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr13:113530143 C>T maps to NM_032189.3 S1072S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr14:56755237 C>T maps to NM_021255.2 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr14:56755237 C>T maps to NM_021255.2 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr14:103371926 C>T maps to NM_145725.2 R505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr14:103371926 C>T maps to NM_145725.2 R505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr16:2258606 C>T maps to NM_022372.4 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr16:2258606 C>T maps to NM_022372.4 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr17:7751610 C>T maps to NM_001080424.1 R669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr17:7751610 C>T maps to NM_001080424.1 R669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr17:42427093 C>T maps to NM_002087.2 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr17:42427093 C>T maps to NM_002087.2 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr17:76851859 G>A maps to NM_003255.4 N184N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr17:76851859 G>A maps to NM_003255.4 N184N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr17:78389500 G>A maps to NM_173627.3 W36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr17:78389500 G>A maps to NM_173627.3 W36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr18:9535826 G>A maps to NM_006788.3 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr18:9535826 G>A maps to NM_006788.3 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr19:10887830 G>C maps to NM_001005361.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr19:10887830 G>C maps to NM_001005361.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr19:12126250 C>T maps to NM_001080411.1 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr19:12126250 C>T maps to NM_001080411.1 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr19:20228641 T>C maps to NM_007138.1 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr19:20228641 T>C maps to NM_007138.1 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr2:9770491 G>C maps to NM_006826.2 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr2:9770491 G>C maps to NM_006826.2 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr2:231973476 C>A maps to NM_000867.4 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr2:231973476 C>A maps to NM_000867.4 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr20:30310085 G>A did not map to a codon.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr20:30310085 G>A did not map to a codon.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr22:38154081 C>G maps to NM_001039141.2 L2050L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr22:38154081 C>G maps to NM_001039141.2 L2050L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr3:14960292 C>A maps to NM_152536.3 Y1174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr3:14960292 C>A maps to NM_152536.3 Y1174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr4:88973182 C>G maps to NM_000297.2 S530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr4:88973182 C>G maps to NM_000297.2 S530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr5:13871016 G>A maps to NM_001369.2 N1231N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr5:13871016 G>A maps to NM_001369.2 N1231N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr5:169508957 G>A maps to NM_004946.2 R1800R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr5:169508957 G>A maps to NM_004946.2 R1800R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr6:155145426 G>A maps to NM_014892.3 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr6:155145426 G>A maps to NM_014892.3 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr7:143956022 C>T maps to NM_001005328.1 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr7:143956022 C>T maps to NM_001005328.1 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr9:35044335 G>A maps to NM_203299.2 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr9:35044335 G>A maps to NM_203299.2 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr1:32089282 C>T maps to NM_001525.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr1:32089282 C>T maps to NM_001525.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr1:35365841 G>A maps to NM_001080418.1 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr1:35365841 G>A maps to NM_001080418.1 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr1:173155864 G>A maps to NM_003326.3 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr1:173155864 G>A maps to NM_003326.3 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr1:176998824 G>A maps to ENST00000281881 N355N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr1:176998824 G>A maps to ENST00000281881 N355N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr1:226027610 C>T maps to NM_001136018.2 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr1:226027610 C>T maps to NM_001136018.2 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr10:5435650 C>T maps to NM_024803.2 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr10:5435650 C>T maps to NM_024803.2 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr11:102988372 A>T maps to NM_001080463.1 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr11:102988372 A>T maps to NM_001080463.1 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr12:14927721 C>T maps to NM_177925.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr12:14927721 C>T maps to NM_177925.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr17:5357144 G>A maps to ENST00000457531 Q494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr17:5357144 G>A maps to ENST00000457531 Q494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr17:79108260 G>A maps to NM_001080395.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr17:79108260 G>A maps to NM_001080395.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr2:54483228 C>T maps to NM_001003937.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr2:54483228 C>T maps to NM_001003937.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr2:100055564 C>T maps to NM_016316.2 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr2:100055564 C>T maps to NM_016316.2 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr2:102636164 C>T maps to NM_004633.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr2:102636164 C>T maps to NM_004633.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr2:136566781 G>A maps to NM_002299.2 Y1045Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr2:136566781 G>A maps to NM_002299.2 Y1045Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr20:1629752 C>T maps to NM_018556.3 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr20:1629752 C>T maps to NM_018556.3 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr4:52862053 C>T maps to NM_001024611.1 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr4:52862053 C>T maps to NM_001024611.1 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr7:23213805 C>T maps to NM_001031710.2 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr7:23213805 C>T maps to NM_001031710.2 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr7:101844778 C>T maps to ENST00000360264 S745S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr7:101844778 C>T maps to ENST00000360264 S745S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chrX:109943926 T>C maps to NM_001143981.1 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chrX:109943926 T>C maps to NM_001143981.1 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chrX:155233407 A>G maps to NM_002186.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5247-01A-01D-2012-08 chrX:155233407 A>G maps to NM_002186.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:19453066 G>C maps to ENST00000375267 S3104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:19453066 G>C maps to ENST00000375267 S3104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:19992626 C>G maps to NM_000871.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:19992626 C>G maps to NM_000871.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:25153551 C>T maps to NM_013943.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:25153551 C>T maps to NM_013943.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:35917292 G>T maps to NM_024874.4 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:35917292 G>T maps to NM_024874.4 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:36291378 G>T maps to NM_017629.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:36291378 G>T maps to NM_017629.2 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:43778210 C>G maps to NM_005424.2 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:43778210 C>G maps to NM_005424.2 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:112524370 G>A maps to ENST00000315987 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:112524370 G>A maps to ENST00000315987 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:114442907 G>C maps to NM_006594.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:114442907 G>C maps to NM_006594.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:155238103 T>C maps to ENST00000368361 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:155238103 T>C maps to ENST00000368361 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:166819357 G>C maps to NM_017542.3 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:166819357 G>C maps to NM_017542.3 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:196309571 G>T maps to NM_198503.2 S561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr1:196309571 G>T maps to NM_198503.2 S561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr10:75567372 A>G maps to NM_003635.3 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr10:75567372 A>G maps to NM_003635.3 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr10:81063877 C>T maps to NM_020338.3 I744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr10:81063877 C>T maps to NM_020338.3 I744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr10:112837978 G>C maps to NM_000681.3 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr10:112837978 G>C maps to NM_000681.3 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr10:134165109 G>A did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr10:134165109 G>A did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:6262987 G>A maps to NM_001037329.2 E415E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:6262987 G>A maps to NM_001037329.2 E415E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:51515815 C>T maps to NM_001004703.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:51515815 C>T maps to NM_001004703.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:57003608 G>T maps to NM_005161.4 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:57003608 G>T maps to NM_005161.4 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:64009963 C>G maps to NM_057092.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:64009963 C>G maps to NM_057092.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:65380699 G>T maps to NM_002419.3 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:65380699 G>T maps to NM_002419.3 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:67200086 G>A maps to NM_003952.2 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:67200086 G>A maps to NM_003952.2 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:122720854 G>A maps to NM_019604.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr11:122720854 G>A maps to NM_019604.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr12:8074140 G>A maps to NM_006931.2 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr12:8074140 G>A maps to NM_006931.2 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr12:55820432 C>A maps to NM_001005183.1 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr12:55820432 C>A maps to NM_001005183.1 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr12:56522297 G>C maps to NM_001184796.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr12:56522297 G>C maps to NM_001184796.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr12:70963580 G>A maps to NM_001109754.1 Q1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr12:70963580 G>A maps to NM_001109754.1 Q1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr12:112605282 G>A maps to NM_001109662.2 F3952F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr12:112605282 G>A maps to NM_001109662.2 F3952F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr12:132554095 G>A maps to ENST00000333577 A3013A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr12:132554095 G>A maps to ENST00000333577 A3013A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr13:25840347 G>C maps to NM_004685.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr13:25840347 G>C maps to NM_004685.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr13:41517196 G>A maps to NM_172373.3 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr13:41517196 G>A maps to NM_172373.3 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr14:33147557 T>G maps to NM_004274.4 A924A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr14:33147557 T>G maps to NM_004274.4 A924A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr14:51411034 C>T maps to NM_002863.4 K29K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr14:51411034 C>T maps to NM_002863.4 K29K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CR-5248-01A-01D-2012-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-CR-5248-01A-01D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr14:102805528 G>A maps to NM_018335.3 E632E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr14:102805528 G>A maps to NM_018335.3 E632E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr14:104209071 C>T maps to NM_015316.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr14:104209071 C>T maps to NM_015316.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr14:105414034 G>A maps to NM_138420.2 Q2585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr14:105414034 G>A maps to NM_138420.2 Q2585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr15:59911579 C>G maps to NM_004751.2 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr15:59911579 C>G maps to NM_004751.2 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr15:74659878 G>T maps to NM_000781.2 C16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr15:74659878 G>T maps to NM_000781.2 C16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr15:89802002 C>T maps to NM_001113378.1 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr15:89802002 C>T maps to NM_001113378.1 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr16:16255390 C>T maps to NM_001171.5 G1179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr16:16255390 C>T maps to NM_001171.5 G1179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr16:23706159 G>A maps to NM_033266.3 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr16:23706159 G>A maps to NM_033266.3 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr16:27480792 C>G maps to NM_001520.3 R1631R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr16:27480792 C>G maps to NM_001520.3 R1631R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr16:30794730 G>A maps to NM_001080417.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr16:30794730 G>A maps to NM_001080417.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr16:68712541 G>T maps to NM_001793.4 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr16:68712541 G>T maps to NM_001793.4 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:4843163 C>A maps to NM_003562.4 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:4843163 C>A maps to NM_003562.4 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:17399348 G>A maps to NM_016084.3 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:17399348 G>A maps to NM_016084.3 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:18525852 T>C did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:18525852 T>C did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:33738500 C>T maps to NM_018042.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:33738500 C>T maps to NM_018042.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:55075840 G>T maps to NM_021626.2 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:55075840 G>T maps to NM_021626.2 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:56276416 G>A maps to NM_000502.4 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:56276416 G>A maps to NM_000502.4 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:56403659 C>T maps to NM_004758.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:56403659 C>T maps to NM_004758.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:74077660 C>T maps to NM_180990.3 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr17:74077660 C>T maps to NM_180990.3 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr18:42531992 C>T maps to NM_015559.2 F896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr18:42531992 C>T maps to NM_015559.2 F896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:579569 C>T maps to NM_001728.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:579569 C>T maps to NM_001728.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:1800406 G>A maps to NM_138813.2 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:1800406 G>A maps to NM_138813.2 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:9237044 G>A maps to NM_001001958.1 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:9237044 G>A maps to NM_001001958.1 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:16314373 C>T maps to NM_001130524.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:16314373 C>T maps to NM_001130524.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:20002712 G>A maps to NM_021047.2 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:20002712 G>A maps to NM_021047.2 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:30934666 G>A maps to NM_014717.1 E66E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:30934666 G>A maps to NM_014717.1 E66E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:42482829 G>A maps to ENST00000441343 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:42482829 G>A maps to ENST00000441343 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:44590113 C>A maps to NM_001037813.2 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:44590113 C>A maps to NM_001037813.2 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:50208328 C>T maps to NM_152359.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:50208328 C>T maps to NM_152359.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:54496184 G>A maps to NM_145814.1 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:54496184 G>A maps to NM_145814.1 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:58991810 G>A maps to NM_017908.2 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr19:58991810 G>A maps to NM_017908.2 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr2:43451805 C>T maps to NM_006887.4 Q379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr2:43451805 C>T maps to NM_006887.4 Q379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr2:48687278 C>T maps to NM_001135629.2 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr2:48687278 C>T maps to NM_001135629.2 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr2:71211739 G>C did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr2:71211739 G>C did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr2:222428964 G>A maps to NM_004438.3 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr2:222428964 G>A maps to NM_004438.3 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr2:232262648 C>T maps to NM_145236.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr2:232262648 C>T maps to NM_145236.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr20:40045304 G>A maps to NM_032221.3 R2137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr20:40045304 G>A maps to NM_032221.3 R2137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr20:45354421 C>T maps to NM_030777.3 N249N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr20:45354421 C>T maps to NM_030777.3 N249N. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CR-5248-01A-01D-2012-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-CR-5248-01A-01D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr20:62597951 G>A maps to NM_020713.1 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr20:62597951 G>A maps to NM_020713.1 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr21:46320372 G>A maps to NM_000211.3 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr21:46320372 G>A maps to NM_000211.3 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr22:21134214 G>A maps to NM_000185.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr22:21134214 G>A maps to NM_000185.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr22:29706632 G>C maps to NM_152236.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr22:29706632 G>C maps to NM_152236.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr22:31333849 G>A maps to ENST00000397641 R441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr22:31333849 G>A maps to ENST00000397641 R441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr22:50500059 G>A maps to NM_015166.3 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr22:50500059 G>A maps to NM_015166.3 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr22:50927675 C>T maps to NM_017584.5 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr22:50927675 C>T maps to NM_017584.5 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr3:8607272 A>C maps to NM_014583.2 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr3:8607272 A>C maps to NM_014583.2 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr3:37048480 G>C did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr3:37048480 G>C did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr3:49948246 C>T maps to NM_032355.3 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr3:49948246 C>T maps to NM_032355.3 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr3:101373662 C>A maps to NM_014415.3 E732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr3:101373662 C>A maps to NM_014415.3 E732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr3:148858877 G>T maps to NM_032383.3 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr3:148858877 G>T maps to NM_032383.3 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr3:151154851 A>G maps to NM_178822.4 Y2499Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr3:151154851 A>G maps to NM_178822.4 Y2499Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr3:157146230 C>T maps to NM_001167912.1 Q192Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr3:157146230 C>T maps to NM_001167912.1 Q192Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr4:20530584 T>C maps to ENST00000273739 Y496Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr4:20530584 T>C maps to ENST00000273739 Y496Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr4:56301652 G>A maps to NM_004898.2 Q824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr4:56301652 G>A maps to NM_004898.2 Q824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr5:13871061 G>A maps to NM_001369.2 V1216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr5:13871061 G>A maps to NM_001369.2 V1216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr5:14291309 G>A maps to NM_007118.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr5:14291309 G>A maps to NM_007118.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr5:71654229 C>G maps to NM_024754.3 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr5:71654229 C>G maps to NM_024754.3 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr5:96130757 G>A maps to NM_016442.3 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr5:96130757 G>A maps to NM_016442.3 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr5:131530706 A>C maps to NM_001142599.1 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr5:131530706 A>C maps to NM_001142599.1 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr6:13487001 C>A maps to NM_018988.2 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr6:13487001 C>A maps to NM_018988.2 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr6:41126779 G>A maps to NM_018965.2 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr6:41126779 G>A maps to NM_018965.2 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr6:50803960 C>T maps to ENST00000263046 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr6:50803960 C>T maps to ENST00000263046 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr6:70411788 G>A maps to NM_018368.3 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr6:70411788 G>A maps to NM_018368.3 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr6:119252639 G>A maps to ENST00000316316 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr6:119252639 G>A maps to ENST00000316316 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr6:137019685 G>A maps to NM_005923.3 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr6:137019685 G>A maps to NM_005923.3 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr7:5232765 C>G maps to NM_015610.3 S31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr7:5232765 C>G maps to NM_015610.3 S31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr7:26224728 G>T maps to NM_004289.6 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr7:26224728 G>T maps to NM_004289.6 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr7:127222319 G>A maps to NM_024523.5 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr7:127222319 G>A maps to NM_024523.5 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr7:134916759 C>G maps to NM_182489.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr7:134916759 C>G maps to NM_182489.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr7:141952097 G>T maps to NM_001001317.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr7:141952097 G>T maps to NM_001001317.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr8:33357859 G>A maps to NM_001102401.1 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr8:33357859 G>A maps to NM_001102401.1 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr8:43053069 G>A maps to ENST00000458501 W595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr8:43053069 G>A maps to ENST00000458501 W595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr8:65517374 G>C maps to NM_004820.3 S366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr8:65517374 G>C maps to NM_004820.3 S366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr8:145623785 G>A maps to NM_013291.2 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr8:145623785 G>A maps to NM_013291.2 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr9:368026 C>G maps to NM_203447.3 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr9:368026 C>G maps to NM_203447.3 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr9:5922658 G>A maps to NM_001017969.2 Q1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr9:5922658 G>A maps to NM_001017969.2 Q1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr9:88247623 C>T maps to ENST00000395847 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr9:88247623 C>T maps to ENST00000395847 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr9:130263292 G>A maps to NM_001005374.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr9:130263292 G>A maps to NM_001005374.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr9:136260785 C>A maps to NM_153710.3 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr9:136260785 C>A maps to NM_153710.3 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chrX:35974177 C>T maps to NM_152632.3 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chrX:35974177 C>T maps to NM_152632.3 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chrX:152936780 C>T maps to NM_001039582.3 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chrX:152936780 C>T maps to NM_001039582.3 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr10:43318579 T>A maps to NM_014753.3 S1049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr10:43318579 T>A maps to NM_014753.3 S1049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr10:129877949 G>A maps to NM_006504.4 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr10:129877949 G>A maps to NM_006504.4 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr11:121178028 T>C maps to NM_001024956.2 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr11:121178028 T>C maps to NM_001024956.2 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr14:31602802 C>T maps to NM_015382.2 G1219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr14:31602802 C>T maps to NM_015382.2 G1219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr14:55168921 T>C maps to NM_015589.4 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr14:55168921 T>C maps to NM_015589.4 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr16:69922038 C>A maps to NM_007014.3 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr16:69922038 C>A maps to NM_007014.3 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr16:75512886 C>T maps to NM_021615.4 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr16:75512886 C>T maps to NM_021615.4 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr17:48070808 G>A maps to NM_005220.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr17:48070808 G>A maps to NM_005220.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr18:8825332 G>A maps to ENST00000456698 E1594E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr18:8825332 G>A maps to ENST00000456698 E1594E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr19:7605583 G>A maps to NM_001166111.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr19:7605583 G>A maps to NM_001166111.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr19:10793295 G>A maps to NM_017620.2 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr19:10793295 G>A maps to NM_017620.2 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr19:13368241 G>T maps to NM_023035.2 I1508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr19:13368241 G>T maps to NM_023035.2 I1508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr19:37904080 G>T maps to NM_152484.2 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr19:37904080 G>T maps to NM_152484.2 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr2:96970570 G>A maps to NM_014014.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr2:96970570 G>A maps to NM_014014.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr20:62340306 C>T maps to NM_032527.4 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr20:62340306 C>T maps to NM_032527.4 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr3:164906485 A>G maps to NM_014926.2 D711D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr3:164906485 A>G maps to NM_014926.2 D711D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr6:127911330 A>G maps to NM_001010905.1 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr6:127911330 A>G maps to NM_001010905.1 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr6:152461284 G>A maps to NM_182961.2 R8420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr6:152461284 G>A maps to NM_182961.2 R8420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr7:90895604 C>T maps to NM_003505.1 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr7:90895604 C>T maps to NM_003505.1 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr12:104107481 C>A maps to NM_017564.9 T1491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr12:104107481 C>A maps to NM_017564.9 T1491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr15:29346704 C>T maps to NM_005503.3 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr15:29346704 C>T maps to NM_005503.3 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr15:68504042 G>A maps to NM_017882.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr15:68504042 G>A maps to NM_017882.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr2:27886557 A>G did not map to a codon.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr2:27886557 A>G did not map to a codon.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr2:168106778 G>A maps to NM_152381.5 S2959S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr2:168106778 G>A maps to NM_152381.5 S2959S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr3:11600119 G>A maps to NM_014667.2 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr3:11600119 G>A maps to NM_014667.2 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr7:44098508 C>T maps to NM_001122956.1 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr7:44098508 C>T maps to NM_001122956.1 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr7:94057677 C>T maps to NM_000089.3 G1200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chr7:94057677 C>T maps to NM_000089.3 G1200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chrX:134494850 G>A maps to NM_152695.5 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5250-01A-01D-1512-08 chrX:134494850 G>A maps to NM_152695.5 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr1:152732234 C>T maps to NM_001025231.1 C57C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr1:152732234 C>T maps to NM_001025231.1 C57C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr11:6630567 G>A maps to NM_001014795.1 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr11:6630567 G>A maps to NM_001014795.1 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr13:92345949 C>T maps to NM_004466.4 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr13:92345949 C>T maps to NM_004466.4 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr17:7668742 G>A maps to NM_020877.2 W1124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr17:7668742 G>A maps to NM_020877.2 W1124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr17:73753344 C>T maps to NM_001005619.1 S1744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr17:73753344 C>T maps to NM_001005619.1 S1744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr18:30969507 A>C maps to NM_001105528.1 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr18:30969507 A>C maps to NM_001105528.1 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr18:43666160 G>A maps to NM_001001937.1 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr18:43666160 G>A maps to NM_001001937.1 F449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr19:3752700 C>G maps to NM_004886.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr19:3752700 C>G maps to NM_004886.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr2:141267497 G>A maps to NM_018557.2 C2799C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr2:141267497 G>A maps to NM_018557.2 C2799C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr2:220435108 C>T maps to NM_015311.2 E282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr2:220435108 C>T maps to NM_015311.2 E282E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr20:35399489 G>A maps to NM_001145315.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr20:35399489 G>A maps to NM_001145315.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr22:20458537 G>A maps to NM_015672.1 Q922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr22:20458537 G>A maps to NM_015672.1 Q922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr4:80247010 C>T maps to NM_032693.2 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr4:80247010 C>T maps to NM_032693.2 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr4:121957685 G>A maps to NM_024574.3 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr4:121957685 G>A maps to NM_024574.3 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr4:141583130 A>T maps to NM_015130.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr4:141583130 A>T maps to NM_015130.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr4:187074900 C>T maps to ENST00000356371 C354C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr4:187074900 C>T maps to ENST00000356371 C354C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr6:30571951 C>T maps to NM_002714.2 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr6:30571951 C>T maps to NM_002714.2 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr7:6077065 G>A maps to NM_014413.3 R441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr7:6077065 G>A maps to NM_014413.3 R441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr7:53103444 C>T maps to NM_182595.3 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr7:53103444 C>T maps to NM_182595.3 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr8:21851878 T>A maps to ENST00000434536 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr8:21851878 T>A maps to ENST00000434536 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr8:37986387 G>A maps to NM_004674.3 Q482Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr8:37986387 G>A maps to NM_004674.3 Q482Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr8:123966104 C>T maps to NM_014943.3 N785N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr8:123966104 C>T maps to NM_014943.3 N785N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr9:19619580 C>T did not map to a codon.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr9:19619580 C>T did not map to a codon.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr9:128347841 C>T maps to NM_001006617.1 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr9:128347841 C>T maps to NM_001006617.1 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr9:134367623 C>T maps to NM_013318.3 P2150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6467-01A-11D-1870-08 chr9:134367623 C>T maps to NM_013318.3 P2150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr1:31212768 G>A maps to NM_006762.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr1:31212768 G>A maps to NM_006762.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr1:39749132 G>A maps to ENST00000361689 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr1:39749132 G>A maps to ENST00000361689 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr1:75685019 C>T maps to NM_152697.4 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr1:75685019 C>T maps to NM_152697.4 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr1:109271296 C>T maps to NM_001144937.1 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr1:109271296 C>T maps to NM_001144937.1 F471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr1:236195923 C>A maps to NM_002508.2 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr1:236195923 C>A maps to NM_002508.2 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr1:236766583 G>A maps to NM_018072.5 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr1:236766583 G>A maps to NM_018072.5 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr10:29801692 G>A maps to NM_021738.2 Q1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr10:29801692 G>A maps to NM_021738.2 Q1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr22:40283602 G>C maps to NM_152512.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr22:40283602 G>C maps to NM_152512.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr3:149684320 C>T maps to NM_053024.3 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr3:149684320 C>T maps to NM_053024.3 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr3:172501695 C>T maps to ENST00000392692 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr3:172501695 C>T maps to ENST00000392692 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr6:123869614 G>A maps to NM_006073.2 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr6:123869614 G>A maps to NM_006073.2 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr7:91758199 A>G maps to NM_000786.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6470-01A-11D-1870-08 chr7:91758199 A>G maps to NM_000786.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr1:12954577 A>G maps to NM_001039361.3 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr1:12954577 A>G maps to NM_001039361.3 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr1:22923820 C>T maps to NM_020526.3 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr1:22923820 C>T maps to NM_020526.3 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr1:33235676 C>G maps to NM_020888.2 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr1:33235676 C>G maps to NM_020888.2 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr1:196309632 G>A maps to NM_198503.2 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr1:196309632 G>A maps to NM_198503.2 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr1:242020735 A>G maps to NM_006027.4 Q165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr1:242020735 A>G maps to NM_006027.4 Q165Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr10:82403806 A>C maps to NM_207372.2 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr10:82403806 A>C maps to NM_207372.2 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr10:104835933 G>A maps to NM_017649.3 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr10:104835933 G>A maps to NM_017649.3 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr12:330577 G>A maps to NM_016615.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr12:330577 G>A maps to NM_016615.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr12:10954989 G>A maps to NM_023919.2 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr12:10954989 G>A maps to NM_023919.2 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr13:27257004 G>A maps to NM_006646.5 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr13:27257004 G>A maps to NM_006646.5 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr13:99476708 G>T maps to ENST00000428223 I1691I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr13:99476708 G>T maps to ENST00000428223 I1691I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr15:65621832 T>G maps to NM_004884.3 G700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr15:65621832 T>G maps to NM_004884.3 G700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr15:89398653 C>T maps to NM_013227.3 G946G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr15:89398653 C>T maps to NM_013227.3 G946G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr16:1538462 C>T maps to NM_001013658.1 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr16:1538462 C>T maps to NM_001013658.1 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr16:3781252 G>C maps to NM_004380.2 V1704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr16:3781252 G>C maps to NM_004380.2 V1704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr16:11114116 G>A maps to ENST00000409790 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr16:11114116 G>A maps to ENST00000409790 E457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr16:20856093 C>G maps to NM_030941.2 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr16:20856093 C>G maps to NM_030941.2 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr16:25258085 G>A maps to NM_001012981.4 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr16:25258085 G>A maps to NM_001012981.4 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr16:30980948 G>A maps to NM_014712.1 E985E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr16:30980948 G>A maps to NM_014712.1 E985E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr17:27423780 C>T maps to NM_078471.3 R1461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr17:27423780 C>T maps to NM_078471.3 R1461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr18:2732450 A>G maps to NM_015295.2 R1079R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr18:2732450 A>G maps to NM_015295.2 R1079R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr18:45394804 G>A maps to NM_001003652.2 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr18:45394804 G>A maps to NM_001003652.2 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr19:11942500 A>G maps to NM_152357.2 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr19:11942500 A>G maps to NM_152357.2 K170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr19:12541095 G>A maps to NM_005815.4 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr19:12541095 G>A maps to NM_005815.4 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr2:179197684 A>T maps to ENST00000392505 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr2:179197684 A>T maps to ENST00000392505 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr20:1456847 G>T maps to NM_001122962.1 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr20:1456847 G>T maps to NM_001122962.1 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr3:33255547 C>T maps to NM_015551.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr3:33255547 C>T maps to NM_015551.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr3:47163557 G>A maps to NM_014159.6 I856I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr3:47163557 G>A maps to NM_014159.6 I856I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr3:98001946 C>G maps to NM_001005482.1 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr3:98001946 C>G maps to NM_001005482.1 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr3:184714190 G>T maps to ENST00000437079 S1246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr3:184714190 G>T maps to ENST00000437079 S1246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr3:188242515 T>C maps to NM_005578.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr3:188242515 T>C maps to NM_005578.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr3:194061982 G>A maps to NM_001080513.2 Y483Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr3:194061982 G>A maps to NM_001080513.2 Y483Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr4:74284001 G>A maps to NM_000477.5 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr4:74284001 G>A maps to NM_000477.5 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr4:104017354 G>C maps to NM_020139.3 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr4:104017354 G>C maps to NM_020139.3 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr5:2748624 G>A maps to NM_033267.4 N399N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr5:2748624 G>A maps to NM_033267.4 N399N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr5:102895787 T>G maps to NM_031438.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr5:102895787 T>G maps to NM_031438.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr5:140215782 G>T maps to NM_018910.2 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr5:140215782 G>T maps to NM_018910.2 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr5:171774316 C>T maps to NM_001017995.2 Q344Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr5:171774316 C>T maps to NM_001017995.2 Q344Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr6:34029791 G>T maps to NM_000841.1 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr6:34029791 G>T maps to NM_000841.1 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr6:52268775 C>T maps to ENST00000361841 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr6:52268775 C>T maps to ENST00000361841 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr6:107019899 G>A maps to NM_032730.4 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr6:107019899 G>A maps to NM_032730.4 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr6:138539372 G>A maps to NM_021635.2 R54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr6:138539372 G>A maps to NM_021635.2 R54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr7:2946385 G>A maps to NM_032415.4 Y1117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr7:2946385 G>A maps to NM_032415.4 Y1117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr7:103270589 C>T maps to ENST00000428762 K833K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr7:103270589 C>T maps to ENST00000428762 K833K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr7:105099647 G>A maps to NM_019042.3 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr7:105099647 G>A maps to NM_019042.3 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr8:8749413 G>A maps to NM_004225.2 C385C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr8:8749413 G>A maps to NM_004225.2 C385C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr8:103281236 C>A maps to NM_015902.4 E2444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr8:103281236 C>A maps to NM_015902.4 E2444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr8:145139717 C>T maps to NM_003801.3 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr8:145139717 C>T maps to NM_003801.3 F368F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:6698378 C>T maps to NM_018198.3 Q433Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:6698378 C>T maps to NM_018198.3 Q433Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:21903030 G>A maps to NM_000478.4 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:21903030 G>A maps to NM_000478.4 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:35921703 G>A maps to NM_024874.4 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:35921703 G>A maps to NM_024874.4 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:47182006 G>C maps to NM_014774.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:47182006 G>C maps to NM_014774.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:53692755 G>A maps to NM_002370.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:53692755 G>A maps to NM_002370.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:66058501 A>C maps to NM_002303.5 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:66058501 A>C maps to NM_002303.5 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:101704695 C>T maps to NM_001400.4 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:101704695 C>T maps to NM_001400.4 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:110294643 C>T maps to NM_139053.1 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:110294643 C>T maps to NM_139053.1 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:112309283 G>A maps to NM_007204.4 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:112309283 G>A maps to NM_007204.4 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:145522726 C>A maps to NM_003846.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:145522726 C>A maps to NM_003846.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:171560971 G>T maps to ENST00000392078 E2895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:171560971 G>T maps to ENST00000392078 E2895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:173545822 C>T maps to NM_178527.3 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:173545822 C>T maps to NM_178527.3 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:175360469 C>G maps to NM_003285.2 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:175360469 C>G maps to NM_003285.2 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:176983946 G>A maps to ENST00000281881 N509N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:176983946 G>A maps to ENST00000281881 N509N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:180199672 G>A maps to NM_033343.3 Q3Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:180199672 G>A maps to NM_033343.3 Q3Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:197070879 G>A maps to NM_018136.4 Q2501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:197070879 G>A maps to NM_018136.4 Q2501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:206942022 G>A maps to NM_000572.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:206942022 G>A maps to NM_000572.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:223438080 C>T maps to NM_017982.3 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:223438080 C>T maps to NM_017982.3 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:234546227 G>C maps to NM_005646.3 S1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr1:234546227 G>C maps to NM_005646.3 S1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr10:294370 G>A maps to NM_006624.4 K441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr10:294370 G>A maps to NM_006624.4 K441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr10:6263357 G>C maps to NM_004566.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr10:6263357 G>C maps to NM_004566.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr10:12155014 C>T maps to NM_018706.5 F757F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr10:12155014 C>T maps to NM_018706.5 F757F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr10:75230955 G>A maps to NM_001142353.1 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr10:75230955 G>A maps to NM_001142353.1 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr10:75525643 G>T maps to NM_198597.1 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr10:75525643 G>T maps to NM_198597.1 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr10:105139421 G>T maps to NM_006951.3 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr10:105139421 G>T maps to NM_006951.3 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:747534 C>G maps to NM_006755.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:747534 C>G maps to NM_006755.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:18956205 C>T maps to NM_147199.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:18956205 C>T maps to NM_147199.3 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:55563456 C>T maps to NM_001004735.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:55563456 C>T maps to NM_001004735.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:56950026 C>T maps to NM_001005210.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:56950026 C>T maps to NM_001005210.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:58126449 G>A maps to NM_001005489.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:58126449 G>A maps to NM_001005489.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:58920181 G>T maps to NM_198847.2 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:58920181 G>T maps to NM_198847.2 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:61543820 G>A maps to NM_001127392.1 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:61543820 G>A maps to NM_001127392.1 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:62365498 C>A maps to NM_004739.2 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:62365498 C>A maps to NM_004739.2 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:63487850 C>A maps to ENST00000377819 S626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:63487850 C>A maps to ENST00000377819 S626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:64603994 C>G maps to NM_017525.2 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:64603994 C>G maps to NM_017525.2 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:64662528 C>G maps to ENST00000421419 L1913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:64662528 C>G maps to ENST00000421419 L1913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:68542816 G>A maps to NM_001876.3 Y514Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:68542816 G>A maps to NM_001876.3 Y514Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:73101848 C>G maps to NM_152222.1 S57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:73101848 C>G maps to NM_152222.1 S57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:124180473 G>A maps to NM_001002917.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:124180473 G>A maps to NM_001002917.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:134240999 C>A maps to NM_138342.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr11:134240999 C>A maps to NM_138342.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:6554305 G>A maps to NM_001242.4 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:6554305 G>A maps to NM_001242.4 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:14019073 G>C maps to NM_000834.3 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:14019073 G>C maps to NM_000834.3 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:21629872 G>C maps to NM_032941.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:21629872 G>C maps to NM_032941.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:48888676 G>A maps to NM_152319.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:48888676 G>A maps to NM_152319.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:48919764 G>T maps to NM_001005203.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:48919764 G>T maps to NM_001005203.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:57573151 C>T maps to NM_002332.2 I1593I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:57573151 C>T maps to NM_002332.2 I1593I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:57626333 C>G maps to NM_005412.5 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:57626333 C>G maps to NM_005412.5 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:95603901 C>T maps to NM_018351.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:95603901 C>T maps to NM_018351.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:101794927 G>C maps to NM_001177.3 S83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:101794927 G>C maps to NM_001177.3 S83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:109945504 G>A maps to NM_183415.1 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:109945504 G>A maps to NM_183415.1 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:110246197 G>C maps to NM_021625.4 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr12:110246197 G>C maps to NM_021625.4 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr13:98086795 G>C maps to NM_021033.6 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr13:98086795 G>C maps to NM_021033.6 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:24886198 C>T maps to NM_025081.2 F1748F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:24886198 C>T maps to NM_025081.2 F1748F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:50117105 G>C maps to NM_002692.3 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:50117105 G>C maps to NM_002692.3 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:55625315 C>G maps to NM_014750.4 V599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:55625315 C>G maps to NM_014750.4 V599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:58048117 C>A maps to NM_001080455.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:58048117 C>A maps to NM_001080455.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:70925889 C>G maps to NM_003813.2 V558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:70925889 C>G maps to NM_003813.2 V558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:94756785 C>A maps to NM_001100607.1 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:94756785 C>A maps to NM_001100607.1 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:96783493 G>A maps to NM_018036.5 F1066F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:96783493 G>A maps to NM_018036.5 F1066F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:104206421 G>A maps to NM_015316.2 P777P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr14:104206421 G>A maps to NM_015316.2 P777P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr15:23932340 C>G maps to NM_002487.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr15:23932340 C>G maps to NM_002487.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr15:43020962 G>C maps to NM_138477.2 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr15:43020962 G>C maps to NM_138477.2 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr15:52242002 A>T did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr15:52242002 A>T did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr15:59373349 C>T maps to ENST00000434298 Q722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr15:59373349 C>T maps to ENST00000434298 Q722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr15:85399942 G>A maps to NM_020778.4 Q860Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr15:85399942 G>A maps to NM_020778.4 Q860Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:745765 G>T maps to NM_153350.3 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:745765 G>T maps to NM_153350.3 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:3779047 C>T maps to NM_004380.2 L2000L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:3779047 C>T maps to NM_004380.2 L2000L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:15917114 G>A maps to NM_001040114.1 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:15917114 G>A maps to NM_001040114.1 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:48595295 C>A maps to NM_153029.3 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:48595295 C>A maps to NM_153029.3 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:50325657 C>T maps to NM_001114.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:50325657 C>T maps to NM_001114.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:57954369 G>C maps to NM_001297.4 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:57954369 G>C maps to NM_001297.4 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:58301438 G>T maps to NM_014157.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:58301438 G>T maps to NM_014157.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:67042972 C>G maps to ENST00000326686 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:67042972 C>G maps to ENST00000326686 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:67985729 G>C maps to NM_005072.4 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:67985729 G>C maps to NM_005072.4 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:84444202 C>T maps to ENST00000416219 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr16:84444202 C>T maps to ENST00000416219 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:685476 G>A maps to ENST00000397393 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:685476 G>A maps to ENST00000397393 L210L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CR-6472-01A-11D-1870-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CR-6472-01A-11D-1870-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:28361325 G>T maps to NM_198529.3 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:28361325 G>T maps to NM_198529.3 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:39780614 G>A maps to NM_000422.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:39780614 G>A maps to NM_000422.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:42338012 G>C maps to NM_000342.3 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:42338012 G>C maps to NM_000342.3 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:71281967 G>A maps to NM_012121.4 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:71281967 G>A maps to NM_012121.4 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:73127367 C>T maps to NM_014595.1 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:73127367 C>T maps to NM_014595.1 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:74006417 C>T maps to NM_001988.2 E956E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:74006417 C>T maps to NM_001988.2 E956E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:79954343 G>C maps to ENST00000306729 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr17:79954343 G>C maps to ENST00000306729 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr18:19237109 G>A maps to NM_138340.4 H282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr18:19237109 G>A maps to NM_138340.4 H282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr18:31314317 G>T maps to NM_030632.1 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr18:31314317 G>T maps to NM_030632.1 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr18:60642821 G>A maps to NM_194449.2 L1316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr18:60642821 G>A maps to NM_194449.2 L1316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr18:61064455 C>T maps to NM_004869.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr18:61064455 C>T maps to NM_004869.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:1828052 G>A maps to NM_020695.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:1828052 G>A maps to NM_020695.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:2759261 G>A maps to NM_003021.3 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:2759261 G>A maps to NM_003021.3 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:11517469 G>A maps to NM_001161616.1 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:11517469 G>A maps to NM_001161616.1 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:15224467 G>A maps to NM_033025.4 V634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:15224467 G>A maps to NM_033025.4 V634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:15292502 C>G maps to NM_000435.2 L892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:15292502 C>G maps to NM_000435.2 L892L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:36431158 C>T maps to NM_024509.1 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:36431158 C>T maps to NM_024509.1 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:39962115 C>T maps to NM_003169.3 I599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:39962115 C>T maps to NM_003169.3 I599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:42827883 C>T maps to ENST00000406159 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:42827883 C>T maps to ENST00000406159 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:47597669 C>T maps to NM_015168.1 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:47597669 C>T maps to NM_015168.1 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:49391428 C>A maps to NM_003323.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:49391428 C>A maps to NM_003323.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:50285912 C>T maps to NM_014203.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:50285912 C>T maps to NM_014203.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:50510832 G>C maps to NM_016440.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:50510832 G>C maps to NM_016440.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:27712511 C>T maps to NM_015662.1 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:27712511 C>T maps to NM_015662.1 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:33488458 G>T maps to ENST00000354476 E874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:33488458 G>T maps to ENST00000354476 E874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:47596656 C>T maps to NM_002354.2 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:47596656 C>T maps to NM_002354.2 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:72562090 G>A maps to NM_015189.1 F727F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:72562090 G>A maps to NM_015189.1 F727F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:73928297 G>C maps to NM_016347.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:73928297 G>C maps to NM_016347.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:86276327 G>C maps to NM_015425.3 V810V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:86276327 G>C maps to NM_015425.3 V810V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:97400155 C>G maps to NM_001142292.1 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:97400155 C>G maps to NM_001142292.1 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:152507243 G>A maps to NM_001164507.1 F2357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:152507243 G>A maps to NM_001164507.1 F2357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:179365827 C>T maps to NM_019091.3 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:179365827 C>T maps to NM_019091.3 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:219229376 G>A maps to NM_198559.1 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:219229376 G>A maps to NM_198559.1 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:231742260 G>A maps to NM_030926.4 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr2:231742260 G>A maps to NM_030926.4 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr20:3553416 C>T maps to NM_139321.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr20:3553416 C>T maps to NM_139321.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr20:33862273 G>A maps to NM_006690.3 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr20:33862273 G>A maps to NM_006690.3 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr20:35155432 G>C maps to ENST00000339266 *993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr20:35155432 G>C maps to ENST00000339266 *993S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr20:43374745 G>A maps to ENST00000372861 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr20:43374745 G>A maps to ENST00000372861 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr20:47733707 C>G maps to NM_017453.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr20:47733707 C>G maps to NM_017453.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr20:56188386 C>G did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr20:56188386 C>G did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr20:58571731 G>A maps to NM_177980.2 K645K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr20:58571731 G>A maps to NM_177980.2 K645K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr21:32492802 G>C maps to NM_003253.2 L1553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr21:32492802 G>C maps to NM_003253.2 L1553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr21:32513498 G>A maps to NM_003253.2 I1237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr21:32513498 G>A maps to NM_003253.2 I1237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr21:34787220 C>T maps to ENST00000381995 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr21:34787220 C>T maps to ENST00000381995 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr21:43508452 C>G maps to NM_173568.3 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr21:43508452 C>G maps to NM_173568.3 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr21:46387036 C>A maps to NM_058190.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr21:46387036 C>A maps to NM_058190.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr22:24034854 G>A did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr22:24034854 G>A did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr22:25150054 T>G maps to NM_001008496.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr22:25150054 T>G maps to NM_001008496.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr22:27026411 G>A maps to NM_001886.2 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr22:27026411 G>A maps to NM_001886.2 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr22:36684375 G>A maps to NM_002473.4 D1618D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr22:36684375 G>A maps to NM_002473.4 D1618D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr22:36912641 C>T maps to NM_003753.3 W363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr22:36912641 C>T maps to NM_003753.3 W363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr22:41253201 C>A maps to NM_022098.2 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr22:41253201 C>A maps to NM_022098.2 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:36884181 G>A maps to NM_014831.2 F1693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:36884181 G>A maps to NM_014831.2 F1693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:44903511 G>C maps to NM_144638.1 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:44903511 G>C maps to NM_144638.1 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:118865465 G>T maps to NM_152539.2 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:118865465 G>T maps to NM_152539.2 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:128979528 C>G maps to NM_016128.3 S336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:128979528 C>G maps to NM_016128.3 S336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:130293196 G>A maps to NM_001102608.1 L1125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:130293196 G>A maps to NM_001102608.1 L1125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:142394997 G>C did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:142394997 G>C did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:169540506 G>C maps to NM_001080460.1 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:169540506 G>C maps to NM_001080460.1 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:195256616 C>A maps to NM_006241.4 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr3:195256616 C>A maps to NM_006241.4 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr4:62935974 C>T maps to ENST00000506720 T1364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr4:62935974 C>T maps to ENST00000506720 T1364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr4:66467878 G>C maps to NM_004439.5 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr4:66467878 G>C maps to NM_004439.5 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr4:121957930 G>A maps to NM_024574.3 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr4:121957930 G>A maps to NM_024574.3 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr4:123814216 G>A maps to NM_007083.3 C239C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr4:123814216 G>A maps to NM_007083.3 C239C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:5186270 G>C maps to NM_139056.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:5186270 G>C maps to NM_139056.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:17275435 G>A maps to NM_006317.3 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:17275435 G>A maps to NM_006317.3 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:32712158 C>T maps to ENST00000265074 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:32712158 C>T maps to ENST00000265074 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:95087995 G>A maps to NM_014899.3 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:95087995 G>A maps to NM_014899.3 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:140201500 C>T maps to NM_018908.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:140201500 C>T maps to NM_018908.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:140201579 C>T maps to NM_018908.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:140201579 C>T maps to NM_018908.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:140209499 G>A maps to NM_018909.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:140209499 G>A maps to NM_018909.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:140532107 C>G maps to NM_018939.2 S757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:140532107 C>G maps to NM_018939.2 S757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:140782699 G>T maps to NM_018921.2 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr5:140782699 G>T maps to NM_018921.2 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:25450577 C>T maps to NM_017640.5 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:25450577 C>T maps to NM_017640.5 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:29394965 G>C maps to NM_013937.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:29394965 G>C maps to NM_013937.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:32815406 G>A maps to NM_000593.5 Q656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:32815406 G>A maps to NM_000593.5 Q656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:33660554 C>T maps to ENST00000374316 I2503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:33660554 C>T maps to ENST00000374316 I2503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:39846339 G>C maps to ENST00000398904 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:39846339 G>C maps to ENST00000398904 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:137245832 G>C maps to NM_001008783.1 *417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:137245832 G>C maps to NM_001008783.1 *417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:152644704 G>C maps to NM_182961.2 T5275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:152644704 G>C maps to NM_182961.2 T5275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:170626881 C>G maps to NM_032448.1 S135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr6:170626881 C>G maps to NM_032448.1 S135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:4247912 G>A maps to NM_152744.3 Q1799Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:4247912 G>A maps to NM_152744.3 Q1799Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:4862112 C>T maps to NM_018059.4 W509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:4862112 C>T maps to NM_018059.4 W509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:44555447 G>A maps to NM_013389.2 G1277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:44555447 G>A maps to NM_013389.2 G1277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:51096581 C>A maps to ENST00000395542 G819G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:51096581 C>A maps to ENST00000395542 G819G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:65439418 G>A maps to NM_000181.3 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:65439418 G>A maps to NM_000181.3 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:94230020 G>T maps to NM_001099401.1 S325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:94230020 G>T maps to NM_001099401.1 S325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:99754718 G>A maps to NM_018275.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:99754718 G>A maps to NM_018275.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:100488802 C>T maps to NM_000665.3 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr7:100488802 C>T maps to NM_000665.3 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr8:11706667 G>A maps to NM_147783.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr8:11706667 G>A maps to NM_147783.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr8:124042887 G>C maps to NM_024295.4 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr8:124042887 G>C maps to NM_024295.4 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr8:125078775 G>A maps to NM_001039112.2 L1221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr8:125078775 G>A maps to NM_001039112.2 L1221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr9:18777190 G>A maps to NM_001040272.4 P988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr9:18777190 G>A maps to NM_001040272.4 P988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr9:40772751 G>C maps to NM_033160.5 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr9:40772751 G>C maps to NM_033160.5 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr9:97062207 C>A maps to NM_194320.2 S123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr9:97062207 C>A maps to NM_194320.2 S123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr9:109687760 C>G maps to NM_021224.4 S523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr9:109687760 C>G maps to NM_021224.4 S523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chrX:153296807 G>A maps to NM_001110792.1 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chrX:153296807 G>A maps to NM_001110792.1 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chrX:153580936 G>A maps to NM_001110556.1 L2162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chrX:153580936 G>A maps to NM_001110556.1 L2162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr1:172558718 A>G maps to ENST00000367723 P978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr1:172558718 A>G maps to ENST00000367723 P978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr11:6190884 G>A maps to NM_001004052.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr11:6190884 G>A maps to NM_001004052.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr11:14632513 T>A maps to NM_148976.2 K7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr11:14632513 T>A maps to NM_148976.2 K7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr11:100999747 C>T maps to NM_000926.4 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr11:100999747 C>T maps to NM_000926.4 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr12:49436601 C>A maps to NM_003482.3 E1902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr12:49436601 C>A maps to NM_003482.3 E1902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr13:100635349 C>T maps to NM_007129.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr13:100635349 C>T maps to NM_007129.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr14:21216173 C>T maps to NM_006683.4 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr14:21216173 C>T maps to NM_006683.4 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr14:74125656 C>T maps to NM_031427.2 C50C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr14:74125656 C>T maps to NM_031427.2 C50C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr14:102509066 C>T maps to NM_001376.4 P4165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr14:102509066 C>T maps to NM_001376.4 P4165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr16:1035130 C>T maps to NM_014587.3 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr16:1035130 C>T maps to NM_014587.3 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr19:4793182 G>A maps to NM_018708.2 A439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr19:4793182 G>A maps to NM_018708.2 A439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr19:9084695 C>T maps to NM_024690.2 L2373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr19:9084695 C>T maps to NM_024690.2 L2373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr19:9085595 C>T maps to NM_024690.2 L2073L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr19:9085595 C>T maps to NM_024690.2 L2073L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr19:11657660 C>A maps to NM_001299.4 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr19:11657660 C>A maps to NM_001299.4 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr19:39330891 G>A maps to ENST00000221419 Y359Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr19:39330891 G>A maps to ENST00000221419 Y359Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr19:43763285 C>T maps to NM_002784.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr19:43763285 C>T maps to NM_002784.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr2:1459984 A>G maps to NM_000547.5 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr2:1459984 A>G maps to NM_000547.5 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr2:97274402 T>C did not map to a codon.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr2:97274402 T>C did not map to a codon.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr2:196602679 G>A maps to NM_018897.2 R4014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr2:196602679 G>A maps to NM_018897.2 R4014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr20:31379432 G>A maps to NM_006892.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr20:31379432 G>A maps to NM_006892.3 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr22:20103245 C>T maps to ENST00000439169 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr22:20103245 C>T maps to ENST00000439169 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr3:9877029 C>T maps to NM_001025930.3 R869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr3:9877029 C>T maps to NM_001025930.3 R869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr3:40457534 G>T maps to NM_001248.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr3:40457534 G>T maps to NM_001248.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr3:49149393 G>A maps to ENST00000434032 A949A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr3:49149393 G>A maps to ENST00000434032 A949A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr3:52720818 T>C maps to NM_014366.4 H16H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr3:52720818 T>C maps to NM_014366.4 H16H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr3:52825551 C>T maps to NM_002215.2 I838I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr3:52825551 C>T maps to NM_002215.2 I838I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr3:190026160 G>A maps to NM_021101.4 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr3:190026160 G>A maps to NM_021101.4 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr3:193068903 G>A maps to NM_198505.2 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr3:193068903 G>A maps to NM_198505.2 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr5:71654181 G>A maps to NM_024754.3 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr5:71654181 G>A maps to NM_024754.3 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr5:153429536 G>A maps to NM_005927.4 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr5:153429536 G>A maps to NM_005927.4 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr6:26448954 G>A did not map to a codon.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr6:26448954 G>A did not map to a codon.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr8:67925255 C>T maps to ENST00000421742 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr8:67925255 C>T maps to ENST00000421742 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chrX:122532518 G>A maps to NM_000828.4 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chrX:122532518 G>A maps to NM_000828.4 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr1:11090259 C>A maps to NM_006610.2 E424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr1:11090259 C>A maps to NM_006610.2 E424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr1:75039017 T>C maps to NM_001002912.4 K792K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr1:75039017 T>C maps to NM_001002912.4 K792K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr1:149784912 C>G maps to NM_001123375.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr1:149784912 C>G maps to NM_001123375.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr1:157497569 C>T maps to NM_031281.2 W599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr1:157497569 C>T maps to NM_031281.2 W599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr1:158151353 C>T maps to NM_001766.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr1:158151353 C>T maps to NM_001766.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr10:120917409 G>A maps to NM_213649.1 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr10:120917409 G>A maps to NM_213649.1 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr10:131761668 C>A maps to ENST00000355311 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr10:131761668 C>A maps to ENST00000355311 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr11:1028715 G>T maps to NM_005961.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr11:1028715 G>T maps to NM_005961.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr11:40137505 T>G maps to NM_020929.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr11:40137505 T>G maps to NM_020929.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr11:62655846 G>T maps to NM_001012661.1 R556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr11:62655846 G>T maps to NM_001012661.1 R556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr15:33358885 T>A maps to NM_001103184.2 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr15:33358885 T>A maps to NM_001103184.2 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr15:34648620 A>G maps to ENST00000438749 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr15:34648620 A>G maps to ENST00000438749 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr16:15694393 G>C maps to NM_014647.3 L1568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr16:15694393 G>C maps to NM_014647.3 L1568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr17:691247 G>A maps to NM_018146.2 K201K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr17:691247 G>A maps to NM_018146.2 K201K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr17:2298242 T>G maps to NM_020310.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr17:2298242 T>G maps to NM_020310.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr17:7592166 A>G maps to NM_018081.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr17:7592166 A>G maps to NM_018081.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr17:18156742 C>T maps to NM_002018.2 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr17:18156742 C>T maps to NM_002018.2 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr19:22939993 A>G maps to ENST00000397104 C779C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr19:22939993 A>G maps to ENST00000397104 C779C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr19:35832024 C>T maps to NM_001771.3 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr19:35832024 C>T maps to NM_001771.3 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr2:100210747 C>A maps to NM_001025108.1 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr2:100210747 C>A maps to NM_001025108.1 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr2:215274871 T>C maps to NM_024532.3 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr2:215274871 T>C maps to NM_024532.3 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr2:225652093 T>C maps to NM_014689.2 L1813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr2:225652093 T>C maps to NM_014689.2 L1813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr20:2542576 C>T maps to NM_080751.2 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr20:2542576 C>T maps to NM_080751.2 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr21:46066854 C>T maps to NM_198692.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr21:46066854 C>T maps to NM_198692.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr22:50862015 C>T maps to ENST00000216061 C366C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr22:50862015 C>T maps to ENST00000216061 C366C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr3:155838564 C>G maps to NM_172160.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr3:155838564 C>G maps to NM_172160.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr4:436362 C>T maps to NM_133474.2 Q631Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr4:436362 C>T maps to NM_133474.2 Q631Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr4:7056453 G>A maps to NM_152293.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr4:7056453 G>A maps to NM_152293.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr4:85748034 T>A maps to NM_014991.4 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr4:85748034 T>A maps to NM_014991.4 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr5:41929883 C>T maps to NM_012176.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr5:41929883 C>T maps to NM_012176.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr5:140798772 G>A maps to NM_018927.2 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr5:140798772 G>A maps to NM_018927.2 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr6:90425373 G>A maps to NM_014611.1 F2286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr6:90425373 G>A maps to NM_014611.1 F2286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr6:136597105 C>G maps to NM_014739.2 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr6:136597105 C>G maps to NM_014739.2 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr7:1528987 C>T maps to ENST00000389470 V898V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr7:1528987 C>T maps to ENST00000389470 V898V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr7:143632930 T>G maps to NM_001004685.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chr7:143632930 T>G maps to NM_001004685.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chrX:83357103 G>A maps to NM_014496.4 R573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6474-01A-11D-1870-08 chrX:83357103 G>A maps to NM_014496.4 R573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr1:60505606 C>T maps to NM_152377.2 K243K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr1:60505606 C>T maps to NM_152377.2 K243K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr1:200017504 A>G maps to NM_205860.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr1:200017504 A>G maps to NM_205860.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr10:115923079 G>A did not map to a codon.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr10:115923079 G>A did not map to a codon.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr10:120513992 G>A maps to NM_153810.4 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr10:120513992 G>A maps to NM_153810.4 C94C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr11:71725760 G>A maps to ENST00000393695 Q936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr11:71725760 G>A maps to ENST00000393695 Q936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr11:73584273 G>A maps to NM_016565.2 D50D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr11:73584273 G>A maps to NM_016565.2 D50D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr11:123847714 G>A maps to NM_001004474.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr11:123847714 G>A maps to NM_001004474.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr12:102471260 A>G maps to NM_024057.2 N187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr12:102471260 A>G maps to NM_024057.2 N187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr14:56755319 G>T maps to NM_021255.2 G159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr14:56755319 G>T maps to NM_021255.2 G159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr14:69805440 C>T maps to NM_020692.2 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr14:69805440 C>T maps to NM_020692.2 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr16:2369815 G>A maps to NM_001089.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr16:2369815 G>A maps to NM_001089.2 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr16:67863713 G>A maps to NM_025082.3 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr16:67863713 G>A maps to NM_025082.3 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr17:5042700 T>G maps to NM_004505.2 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr17:5042700 T>G maps to NM_004505.2 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr17:10398331 C>T maps to NM_005963.3 V1794V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr17:10398331 C>T maps to NM_005963.3 V1794V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr17:27937743 G>A maps to NM_152345.4 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr17:27937743 G>A maps to NM_152345.4 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr2:65245372 C>G maps to NM_003038.4 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr2:65245372 C>G maps to NM_003038.4 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr2:179586739 T>C maps to NM_133378.4 K6306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr2:179586739 T>C maps to NM_133378.4 K6306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr22:28193870 G>A maps to NM_002430.2 A887A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr22:28193870 G>A maps to NM_002430.2 A887A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr3:1320175 A>G maps to NM_014461.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr3:1320175 A>G maps to NM_014461.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr3:26751570 G>A maps to NM_052953.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr3:26751570 G>A maps to NM_052953.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr3:28562600 A>G maps to NM_001040432.1 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr3:28562600 A>G maps to NM_001040432.1 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr3:113699547 T>C maps to NM_020817.1 K752K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr3:113699547 T>C maps to NM_020817.1 K752K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr4:106158041 T>A maps to ENST00000513237 I1002I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr4:106158041 T>A maps to ENST00000513237 I1002I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr4:187540778 G>A maps to ENST00000260147 Q2324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr4:187540778 G>A maps to ENST00000260147 Q2324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr5:150925422 A>G maps to NM_001447.2 A1755A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr5:150925422 A>G maps to NM_001447.2 A1755A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CR-6477-01A-11D-1870-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-CR-6477-01A-11D-1870-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr6:154763229 C>T maps to NM_173515.2 W137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr6:154763229 C>T maps to NM_173515.2 W137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr8:10466396 C>A maps to NM_178857.5 G1737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr8:10466396 C>A maps to NM_178857.5 G1737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr8:43173711 C>T maps to NM_001005365.2 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chr8:43173711 C>T maps to NM_001005365.2 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chrX:18593591 G>C maps to NM_001037343.1 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chrX:18593591 G>C maps to NM_001037343.1 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chrX:31950340 T>C maps to ENST00000357033 L2206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6477-01A-11D-1870-08 chrX:31950340 T>C maps to ENST00000357033 L2206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr1:29557400 G>A maps to NM_016011.2 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr1:29557400 G>A maps to NM_016011.2 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr1:45478995 C>T maps to NM_000374.4 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr1:45478995 C>T maps to NM_000374.4 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr1:111731344 G>A maps to NM_024901.3 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr1:111731344 G>A maps to NM_024901.3 Q360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr1:202464746 C>T maps to ENST00000367270 I795I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr1:202464746 C>T maps to ENST00000367270 I795I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr1:248790264 G>A maps to NM_001001964.1 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr1:248790264 G>A maps to NM_001001964.1 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr10:30316178 G>A maps to NM_020848.2 D966D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr10:30316178 G>A maps to NM_020848.2 D966D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr10:61022289 G>A maps to ENST00000442566 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr10:61022289 G>A maps to ENST00000442566 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr10:99340626 C>T maps to NM_020349.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr10:99340626 C>T maps to NM_020349.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr10:101190304 G>A maps to NM_002079.2 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr10:101190304 G>A maps to NM_002079.2 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr10:122668113 G>A maps to NM_018117.11 K1188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr10:122668113 G>A maps to NM_018117.11 K1188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr11:60059778 A>T maps to NM_148975.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr11:60059778 A>T maps to NM_148975.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr11:62294493 G>A maps to NM_001620.1 P2465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr11:62294493 G>A maps to NM_001620.1 P2465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr11:92624270 C>T maps to ENST00000298047 Q4588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr11:92624270 C>T maps to ENST00000298047 Q4588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr11:132081942 C>G maps to NM_001144058.1 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr11:132081942 C>G maps to NM_001144058.1 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr12:20799469 T>C maps to NM_000921.3 Y766Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr12:20799469 T>C maps to NM_000921.3 Y766Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr12:39726144 C>T maps to ENST00000395670 E974E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr12:39726144 C>T maps to ENST00000395670 E974E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr12:49434414 G>A maps to NM_003482.3 Q2380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr12:49434414 G>A maps to NM_003482.3 Q2380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr12:75905361 G>A maps to NM_007043.6 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr12:75905361 G>A maps to NM_007043.6 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr12:81839427 C>T maps to NM_003625.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr12:81839427 C>T maps to NM_003625.2 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr12:104067820 C>T maps to NM_017564.9 F836F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr12:104067820 C>T maps to NM_017564.9 F836F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr16:2522265 C>T maps to NM_006181.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr16:2522265 C>T maps to NM_006181.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr16:67692698 G>A maps to NM_001082486.1 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr16:67692698 G>A maps to NM_001082486.1 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr16:67778206 C>T maps to NM_020850.1 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr16:67778206 C>T maps to NM_020850.1 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr17:27896355 C>T maps to NM_138349.2 Y54Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr17:27896355 C>T maps to NM_138349.2 Y54Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr17:38638645 G>T maps to NM_032865.5 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr17:38638645 G>T maps to NM_032865.5 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr17:41956729 C>A maps to NM_005374.3 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr17:41956729 C>A maps to NM_005374.3 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr18:72914174 A>G maps to NM_175907.4 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr18:72914174 A>G maps to NM_175907.4 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr19:6919743 C>T maps to ENST00000381407 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr19:6919743 C>T maps to ENST00000381407 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr19:10663622 T>A maps to NM_032885.4 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr19:10663622 T>A maps to NM_032885.4 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr19:14707911 C>T maps to ENST00000417570 Y195Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr19:14707911 C>T maps to ENST00000417570 Y195Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr19:14991891 G>A maps to NM_030901.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr19:14991891 G>A maps to NM_030901.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr19:17057902 C>T maps to ENST00000443236 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr19:17057902 C>T maps to ENST00000443236 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr19:31039804 C>T maps to NM_014717.1 S1093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr19:31039804 C>T maps to NM_014717.1 S1093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr2:9008677 A>G maps to NM_138799.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr2:9008677 A>G maps to NM_138799.2 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr2:39485696 G>A maps to NM_003618.2 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr2:39485696 G>A maps to NM_003618.2 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr2:47300992 C>T maps to ENST00000394850 F860F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr2:47300992 C>T maps to ENST00000394850 F860F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr2:97866191 C>T maps to NM_001164315.1 A929A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr2:97866191 C>T maps to NM_001164315.1 A929A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr2:98275415 C>T maps to NM_005735.3 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr2:98275415 C>T maps to NM_005735.3 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr2:201507511 A>G maps to NM_001159.3 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr2:201507511 A>G maps to NM_001159.3 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr22:30824463 C>T maps to ENST00000439838 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr22:30824463 C>T maps to ENST00000439838 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr3:49689518 C>T maps to NM_003458.3 R844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr3:49689518 C>T maps to NM_003458.3 R844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr3:121206398 G>A maps to ENST00000393672 F1929F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr3:121206398 G>A maps to ENST00000393672 F1929F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr3:141692898 C>T maps to NM_001178139.1 Q218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr3:141692898 C>T maps to NM_001178139.1 Q218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr4:3520616 C>T maps to NM_002337.2 E191E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr4:3520616 C>T maps to NM_002337.2 E191E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr4:36162101 G>A maps to NM_015230.2 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr4:36162101 G>A maps to NM_015230.2 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr4:66197746 C>T maps to NM_004439.5 E984E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr4:66197746 C>T maps to NM_004439.5 E984E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr4:106156427 A>G maps to ENST00000513237 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr4:106156427 A>G maps to ENST00000513237 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr5:115782988 G>A maps to ENST00000257414 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr5:115782988 G>A maps to ENST00000257414 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr5:140188442 C>T maps to NM_018907.2 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr5:140188442 C>T maps to NM_018907.2 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr6:27101059 G>A maps to NM_021064.4 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr6:27101059 G>A maps to NM_021064.4 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr6:29141561 A>T maps to NM_030905.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr6:29141561 A>T maps to NM_030905.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr7:38796566 C>T maps to NM_014396.3 K522K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr7:38796566 C>T maps to NM_014396.3 K522K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr7:42950073 G>A maps to NM_001099858.1 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr7:42950073 G>A maps to NM_001099858.1 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr7:55466317 C>T maps to NM_018697.3 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr7:55466317 C>T maps to NM_018697.3 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr7:100179490 G>A maps to NM_002319.3 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr7:100179490 G>A maps to NM_002319.3 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr8:55372416 C>T maps to NM_022454.3 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr8:55372416 C>T maps to NM_022454.3 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr8:125113502 G>A maps to NM_001039112.2 K1683K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chr8:125113502 G>A maps to NM_001039112.2 K1683K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chrX:134947916 G>T maps to NM_001172288.1 C136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6478-01A-11D-1870-08 chrX:134947916 G>T maps to NM_001172288.1 C136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr1:150724307 G>A maps to NM_004079.4 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr1:150724307 G>A maps to NM_004079.4 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr1:150724457 G>A maps to NM_004079.4 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr1:150724457 G>A maps to NM_004079.4 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr1:178433453 G>A maps to ENST00000263528 E1087E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr1:178433453 G>A maps to ENST00000263528 E1087E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr1:226041386 G>C maps to NM_014698.2 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr1:226041386 G>C maps to NM_014698.2 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr1:236718635 A>G maps to NM_018072.5 P1961P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr1:236718635 A>G maps to NM_018072.5 P1961P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr11:64022743 C>T maps to NM_000932.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr11:64022743 C>T maps to NM_000932.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr11:116661545 C>T maps to NM_052968.4 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr11:116661545 C>T maps to NM_052968.4 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr12:6031928 G>A maps to ENST00000356134 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr12:6031928 G>A maps to ENST00000356134 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr12:12871105 G>A maps to NM_004064.3 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr12:12871105 G>A maps to NM_004064.3 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr15:59172278 T>C maps to NM_024755.2 V1008V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr15:59172278 T>C maps to NM_024755.2 V1008V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr15:66855886 G>A maps to NM_207338.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr15:66855886 G>A maps to NM_207338.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr16:3639416 G>A maps to NM_032444.2 Q1408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr16:3639416 G>A maps to NM_032444.2 Q1408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr16:10995907 T>A maps to NM_000246.3 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr16:10995907 T>A maps to NM_000246.3 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr17:1582625 C>T maps to NM_006445.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr17:1582625 C>T maps to NM_006445.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr17:27943184 G>A maps to ENST00000345068 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr17:27943184 G>A maps to ENST00000345068 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr17:40870630 G>A maps to ENST00000264646 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr17:40870630 G>A maps to ENST00000264646 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr18:77208871 C>T maps to NM_172387.1 Q480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr18:77208871 C>T maps to NM_172387.1 Q480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr19:54080932 C>T maps to NM_001079907.1 H373H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr19:54080932 C>T maps to NM_001079907.1 H373H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr2:18765359 G>A maps to ENST00000455492 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr2:18765359 G>A maps to ENST00000455492 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr2:24302331 C>T maps to NM_147184.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr2:24302331 C>T maps to NM_147184.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr2:74784054 C>A maps to NM_001381.3 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr2:74784054 C>A maps to NM_001381.3 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr2:106498357 A>G maps to NM_001004720.2 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr2:106498357 A>G maps to NM_001004720.2 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr2:178592822 G>A maps to NM_016953.3 A622A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr2:178592822 G>A maps to NM_016953.3 A622A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr20:25657008 G>C maps to NM_015655.2 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr20:25657008 G>C maps to NM_015655.2 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr20:62598781 C>T maps to NM_020713.1 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr20:62598781 C>T maps to NM_020713.1 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr22:22057703 G>A maps to NM_013313.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr22:22057703 G>A maps to NM_013313.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr22:50319134 G>A maps to NM_001135101.1 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr22:50319134 G>A maps to NM_001135101.1 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr3:122629103 G>A maps to NM_001031702.2 F1114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr3:122629103 G>A maps to NM_001031702.2 F1114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr4:30723352 C>T maps to NM_001173523.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr4:30723352 C>T maps to NM_001173523.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr4:169383026 C>T maps to NM_001012967.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr4:169383026 C>T maps to NM_001012967.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr5:137599971 G>A maps to NM_001496.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr5:137599971 G>A maps to NM_001496.3 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr5:138842246 G>A maps to NM_001077693.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr5:138842246 G>A maps to NM_001077693.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr6:8421005 C>T maps to NM_001142540.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr6:8421005 C>T maps to NM_001142540.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr6:56496809 G>C maps to ENST00000361203 L1067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr6:56496809 G>C maps to ENST00000361203 L1067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr7:8196805 A>T maps to ENST00000422063 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr7:8196805 A>T maps to ENST00000422063 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr8:144992203 G>A maps to NM_201380.2 L4066L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr8:144992203 G>A maps to NM_201380.2 L4066L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr9:5968205 G>A maps to NM_001017969.2 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr9:5968205 G>A maps to NM_001017969.2 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr9:33030453 A>G maps to NM_001539.2 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr9:33030453 A>G maps to NM_001539.2 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr9:137734076 C>T maps to NM_000093.3 I1815I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr9:137734076 C>T maps to NM_000093.3 I1815I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chrX:77380863 G>T maps to NM_000291.3 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chrX:77380863 G>T maps to NM_000291.3 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:1390859 C>T maps to NM_001039211.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:1390859 C>T maps to NM_001039211.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:9427561 G>C maps to NM_025106.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:9427561 G>C maps to NM_025106.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:10703258 C>T maps to NM_001079843.1 R1326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:10703258 C>T maps to NM_001079843.1 R1326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:15392163 G>A maps to NM_201628.2 K379K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:15392163 G>A maps to NM_201628.2 K379K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:41481843 C>T maps to NM_144990.3 E386E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:41481843 C>T maps to NM_144990.3 E386E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:41481852 C>T maps to NM_144990.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:41481852 C>T maps to NM_144990.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:47398444 G>C maps to ENST00000371904 S452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:47398444 G>C maps to ENST00000371904 S452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:47840884 C>T maps to NM_016308.2 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:47840884 C>T maps to NM_016308.2 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:53108621 C>T maps to NM_001042693.1 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:53108621 C>T maps to NM_001042693.1 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:75038327 G>T maps to NM_001002912.4 A1022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:75038327 G>T maps to NM_001002912.4 A1022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:76397846 C>A maps to NM_080868.2 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:76397846 C>A maps to NM_080868.2 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:94577115 C>G maps to NM_000350.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:94577115 C>G maps to NM_000350.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:110466424 C>G maps to NM_000757.4 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:110466424 C>G maps to NM_000757.4 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:150634350 C>T maps to ENST00000369003 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:150634350 C>T maps to ENST00000369003 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:161326610 G>A maps to NM_003001.3 W129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:161326610 G>A maps to NM_003001.3 W129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:183775567 C>T maps to NM_015149.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:183775567 C>T maps to NM_015149.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:186275735 G>A maps to NM_005807.3 Q295Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:186275735 G>A maps to NM_005807.3 Q295Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:186315361 G>A maps to NM_003292.2 Q1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:186315361 G>A maps to NM_003292.2 Q1001*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:223990486 C>G maps to NM_001031685.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:223990486 C>G maps to NM_001031685.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:235915331 G>A maps to NM_000081.2 Q2534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr1:235915331 G>A maps to NM_000081.2 Q2534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:22209806 C>A maps to NM_022365.3 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:22209806 C>A maps to NM_022365.3 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:35929112 C>T maps to NM_031866.2 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:35929112 C>T maps to NM_031866.2 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:61840376 C>T did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:61840376 C>T did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:98133494 C>T maps to NM_012465.3 P840P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:98133494 C>T maps to NM_012465.3 P840P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:105819883 G>A maps to NM_000494.3 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:105819883 G>A maps to NM_000494.3 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:116213164 G>A maps to ENST00000277895 Q575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:116213164 G>A maps to ENST00000277895 Q575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:123844324 G>C maps to NM_206862.2 S770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr10:123844324 G>C maps to NM_206862.2 S770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:2433447 C>T maps to ENST00000452833 K799K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:2433447 C>T maps to ENST00000452833 K799K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:46564068 G>A maps to ENST00000458649 Q500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:46564068 G>A maps to ENST00000458649 Q500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:59604755 G>C maps to NM_005142.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:59604755 G>C maps to NM_005142.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:60107352 G>C maps to NM_139249.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:60107352 G>C maps to NM_139249.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:65649790 C>T maps to NM_001335.3 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:65649790 C>T maps to NM_001335.3 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:67220093 G>A maps to NM_206997.1 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:67220093 G>A maps to NM_206997.1 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:67399080 G>A maps to NM_005995.4 Q385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:67399080 G>A maps to NM_005995.4 Q385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:100061930 C>T maps to NM_014361.2 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:100061930 C>T maps to NM_014361.2 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:108106436 C>T maps to NM_000051.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:108106436 C>T maps to NM_000051.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:112071360 C>T maps to NM_031938.4 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr11:112071360 C>T maps to NM_031938.4 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:996422 C>T maps to NM_001184985.1 L2033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:996422 C>T maps to NM_001184985.1 L2033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:6966014 G>A maps to NM_001098536.1 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:6966014 G>A maps to NM_001098536.1 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:11138871 C>T maps to NM_176890.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:11138871 C>T maps to NM_176890.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:22069955 G>C maps to NM_005691.2 S163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:22069955 G>C maps to NM_005691.2 S163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:30876221 G>A maps to NM_001002259.1 Q672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:30876221 G>A maps to NM_001002259.1 Q672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:43846362 G>A maps to ENST00000389420 I632I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:43846362 G>A maps to ENST00000389420 I632I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:50152484 G>A maps to NM_001098576.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:50152484 G>A maps to NM_001098576.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:72335506 C>G maps to ENST00000389376 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:72335506 C>G maps to ENST00000389376 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:110252301 C>T maps to NM_021625.4 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:110252301 C>T maps to NM_021625.4 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:111776183 G>A maps to NM_015267.3 L1097L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:111776183 G>A maps to NM_015267.3 L1097L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:132404536 G>A maps to NM_003565.2 L939L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:132404536 G>A maps to NM_003565.2 L939L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:132498088 C>T maps to ENST00000333577 L1258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:132498088 C>T maps to ENST00000333577 L1258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:133358995 C>T maps to NM_005895.3 E1117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr12:133358995 C>T maps to NM_005895.3 E1117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr13:25263407 G>A maps to NM_001185085.1 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr13:25263407 G>A maps to NM_001185085.1 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr14:45665673 C>T maps to NM_020937.2 F1880F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr14:45665673 C>T maps to NM_020937.2 F1880F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr14:65198092 C>G maps to ENST00000394691 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr14:65198092 C>G maps to ENST00000394691 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr14:73566392 G>T maps to NM_021239.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr14:73566392 G>T maps to NM_021239.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr14:94394756 G>A maps to NM_138344.3 Q104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr14:94394756 G>A maps to NM_138344.3 Q104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr15:28459834 G>A maps to NM_004667.4 L2108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr15:28459834 G>A maps to NM_004667.4 L2108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr15:31323258 C>T maps to NM_002420.4 W996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr15:31323258 C>T maps to NM_002420.4 W996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr15:33359905 G>A maps to NM_001103184.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr15:33359905 G>A maps to NM_001103184.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr15:34648776 C>T maps to ENST00000438749 T846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr15:34648776 C>T maps to ENST00000438749 T846T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr15:43827591 G>A maps to NM_001130858.2 F1194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr15:43827591 G>A maps to NM_001130858.2 F1194F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr15:76496184 C>G maps to NM_152335.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr15:76496184 C>G maps to NM_152335.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:1399438 C>T maps to NM_001001410.2 *313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:1399438 C>T maps to NM_001001410.2 *313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:1816350 C>A maps to NM_015133.3 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:1816350 C>A maps to NM_015133.3 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:2811882 G>T maps to NM_016333.3 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:2811882 G>T maps to NM_016333.3 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:4835883 C>A maps to NM_144605.3 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:4835883 C>A maps to NM_144605.3 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:16286776 G>A maps to NM_001171.5 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:16286776 G>A maps to NM_001171.5 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:58704060 G>A maps to NM_018231.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:58704060 G>A maps to NM_018231.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:67680669 C>T maps to NM_001013838.1 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:67680669 C>T maps to NM_001013838.1 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:89597146 C>T maps to NM_003119.2 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr16:89597146 C>T maps to NM_003119.2 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:4457188 C>G maps to NM_001105538.1 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:4457188 C>G maps to NM_001105538.1 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:4510764 C>T maps to NM_001114974.1 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:4510764 C>T maps to NM_001114974.1 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:8700952 G>A maps to NM_152599.3 R496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:8700952 G>A maps to NM_152599.3 R496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:17409125 G>A maps to NM_148172.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:17409125 G>A maps to NM_148172.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:29162130 G>A maps to NM_024857.3 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:29162130 G>A maps to NM_024857.3 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:29162271 G>A maps to NM_024857.3 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:29162271 G>A maps to NM_024857.3 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:30349316 G>A maps to ENST00000327564 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:30349316 G>A maps to ENST00000327564 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:36704825 C>T maps to NM_025248.2 E1079E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:36704825 C>T maps to NM_025248.2 E1079E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:36876643 G>C maps to NM_005937.3 A725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:36876643 G>C maps to NM_005937.3 A725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:40948651 C>T did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:40948651 C>T did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:42092251 G>A maps to NM_032376.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:42092251 G>A maps to NM_032376.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:43171125 C>G maps to NM_021079.3 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:43171125 C>G maps to NM_021079.3 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:73887414 C>T maps to NM_173547.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:73887414 C>T maps to NM_173547.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:78156548 C>T maps to NM_024110.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:78156548 C>T maps to NM_024110.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:78320512 C>G maps to NM_020914.4 S2842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:78320512 C>G maps to NM_020914.4 S2842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:80674689 C>A maps to NM_024619.3 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:80674689 C>A maps to NM_024619.3 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:80788497 C>T maps to NM_024702.2 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:80788497 C>T maps to NM_024702.2 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:80790149 G>A maps to NM_024702.2 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr17:80790149 G>A maps to NM_024702.2 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:10132364 C>G maps to NM_015725.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:10132364 C>G maps to NM_015725.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:16611791 C>G maps to NM_032207.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:16611791 C>G maps to NM_032207.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:16875992 C>A maps to ENST00000438489 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:16875992 C>A maps to ENST00000438489 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:17875219 G>A maps to NM_015122.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:17875219 G>A maps to NM_015122.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:35828817 G>A maps to NM_001771.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:35828817 G>A maps to NM_001771.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:41828508 C>T maps to NM_052848.1 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:41828508 C>T maps to NM_052848.1 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:46215858 G>A maps to NM_001080469.1 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:46215858 G>A maps to NM_001080469.1 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:49652885 C>G maps to NM_003660.2 S1146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:49652885 C>G maps to NM_003660.2 S1146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:53058568 C>T maps to NM_001039886.3 F800F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr19:53058568 C>T maps to NM_001039886.3 F800F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:1914019 G>A maps to ENST00000399161 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:1914019 G>A maps to ENST00000399161 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:95953209 G>T maps to NM_144707.2 E748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:95953209 G>T maps to NM_144707.2 E748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:101096983 C>T maps to NM_001011717.1 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:101096983 C>T maps to NM_001011717.1 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:124783247 G>A maps to NM_130773.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:124783247 G>A maps to NM_130773.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:159530187 G>A did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:159530187 G>A did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:167262118 C>A maps to NM_002976.2 E1674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:167262118 C>A maps to NM_002976.2 E1674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:202550740 C>T maps to NM_033066.2 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:202550740 C>T maps to NM_033066.2 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:233899031 G>A maps to NM_005383.2 W136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:233899031 G>A maps to NM_005383.2 W136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:235950501 G>A maps to NM_014521.2 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:235950501 G>A maps to NM_014521.2 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr20:42089354 G>C maps to NM_006275.5 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr20:42089354 G>C maps to NM_006275.5 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr20:52199331 G>A maps to NM_006526.2 Q12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr20:52199331 G>A maps to NM_006526.2 Q12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr20:53208153 G>C did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr20:53208153 G>C did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr21:45219457 C>T maps to NM_003683.5 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr21:45219457 C>T maps to NM_003683.5 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr22:19868159 C>A maps to NM_006440.3 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr22:19868159 C>A maps to NM_006440.3 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr22:38028117 G>A maps to ENST00000381756 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr22:38028117 G>A maps to ENST00000381756 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr22:41240868 G>A maps to NM_003932.3 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr22:41240868 G>A maps to NM_003932.3 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr22:42423139 C>T maps to NM_152613.2 N295N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr22:42423139 C>T maps to NM_152613.2 N295N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:33585010 C>T maps to ENST00000359576 L1115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:33585010 C>T maps to ENST00000359576 L1115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:48669701 G>A maps to NM_022911.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:48669701 G>A maps to NM_022911.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:56173587 G>C maps to ENST00000460849 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:56173587 G>C maps to ENST00000460849 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:89259516 C>T maps to NM_005233.5 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:89259516 C>T maps to NM_005233.5 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:122545832 C>T maps to NM_032839.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:122545832 C>T maps to NM_032839.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:133553478 G>A maps to NM_016577.3 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:133553478 G>A maps to NM_016577.3 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:137843366 G>A maps to NM_016161.2 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:137843366 G>A maps to NM_016161.2 F254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:145789108 G>A maps to NM_182943.2 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:145789108 G>A maps to NM_182943.2 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:155199668 G>C maps to ENST00000340059 L1390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:155199668 G>C maps to ENST00000340059 L1390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:183996309 C>A maps to NM_014693.3 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:183996309 C>A maps to NM_014693.3 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:184022097 C>T maps to NM_002808.3 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:184022097 C>T maps to NM_002808.3 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:186450324 C>T maps to NM_001102416.2 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:186450324 C>T maps to NM_001102416.2 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:193185237 C>T maps to NM_032279.2 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:193185237 C>T maps to NM_032279.2 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:196288298 C>G maps to NM_182627.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr3:196288298 C>G maps to NM_182627.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr4:49034612 G>T maps to NM_025087.2 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr4:49034612 G>T maps to NM_025087.2 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr4:57244555 G>A maps to NM_181806.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr4:57244555 G>A maps to NM_181806.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr4:149357541 C>T maps to ENST00000511528 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr4:149357541 C>T maps to ENST00000511528 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr5:50091251 G>A did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr5:50091251 G>A did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr5:66460112 C>T maps to NM_001164664.1 L1702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr5:66460112 C>T maps to NM_001164664.1 L1702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr5:140167977 C>T maps to NM_018900.2 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr5:140167977 C>T maps to NM_018900.2 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr5:140754585 G>C maps to NM_018919.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr5:140754585 G>C maps to NM_018919.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr5:154393877 C>A maps to NM_001099293.1 C153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr5:154393877 C>A maps to NM_001099293.1 C153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:7566621 C>T maps to NM_004415.2 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:7566621 C>T maps to NM_004415.2 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:7570714 C>T maps to NM_004415.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:7570714 C>T maps to NM_004415.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:26124696 C>T maps to NM_003512.3 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:26124696 C>T maps to NM_003512.3 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:27839888 G>A maps to NM_003533.2 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:27839888 G>A maps to NM_003533.2 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:31324664 G>T maps to ENST00000428231 S48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:31324664 G>T maps to ENST00000428231 S48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:33660548 C>T maps to ENST00000374316 F2501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:33660548 C>T maps to ENST00000374316 F2501F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:36938201 G>A maps to ENST00000373627 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:36938201 G>A maps to ENST00000373627 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:43098330 C>T maps to NM_002821.3 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:43098330 C>T maps to NM_002821.3 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:88144768 C>T maps to NM_001031743.2 Q498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:88144768 C>T maps to NM_001031743.2 Q498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:99347182 G>A maps to NM_012160.3 C426C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:99347182 G>A maps to NM_012160.3 C426C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:116988127 C>T maps to NM_145062.2 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:116988127 C>T maps to NM_145062.2 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:133783786 G>A maps to ENST00000452339 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:133783786 G>A maps to ENST00000452339 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:137527278 G>A maps to NM_000416.2 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:137527278 G>A maps to NM_000416.2 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr7:21781777 C>T maps to NM_003777.3 V2723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr7:21781777 C>T maps to NM_003777.3 V2723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr7:37989862 C>A maps to NM_017549.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr7:37989862 C>A maps to NM_017549.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr7:77256780 C>T maps to NM_002835.3 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr7:77256780 C>T maps to NM_002835.3 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr7:100344230 G>A maps to ENST00000349350 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr7:100344230 G>A maps to ENST00000349350 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr7:100816657 C>A maps to NM_198571.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr7:100816657 C>A maps to NM_198571.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr7:133041327 G>A did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr7:133041327 G>A did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:11188897 C>T maps to NM_054028.1 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:11188897 C>T maps to NM_054028.1 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:17419528 C>T maps to NM_001164771.1 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:17419528 C>T maps to NM_001164771.1 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:100147837 C>T maps to NM_017890.3 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:100147837 C>T maps to NM_017890.3 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:100523502 G>T maps to NM_017890.3 E1491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:100523502 G>T maps to NM_017890.3 E1491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:110497289 G>C maps to ENST00000426474 V3198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:110497289 G>C maps to ENST00000426474 V3198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:117874119 C>A maps to NM_006265.2 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:117874119 C>A maps to NM_006265.2 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:123965798 G>A maps to NM_014943.3 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:123965798 G>A maps to NM_014943.3 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:144941997 G>A maps to NM_031308.1 D1808D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:144941997 G>A maps to NM_031308.1 D1808D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:6506133 G>A maps to NM_152896.1 Q788Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:6506133 G>A maps to NM_152896.1 Q788Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:77354767 G>A maps to NM_017662.4 V1786V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:77354767 G>A maps to NM_017662.4 V1786V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:100616543 C>G maps to NM_004473.3 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:100616543 C>G maps to NM_004473.3 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:125438028 G>A maps to NM_001005234.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:125438028 G>A maps to NM_001005234.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:125865490 G>A maps to NM_012197.3 *1070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:125865490 G>A maps to NM_012197.3 *1070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:128001049 C>T maps to NM_005347.4 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:128001049 C>T maps to NM_005347.4 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:134473642 G>A maps to NM_198679.1 D684D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:134473642 G>A maps to NM_198679.1 D684D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:136323095 G>A maps to NM_139025.3 T1319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:136323095 G>A maps to NM_139025.3 T1319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:139391122 G>A maps to NM_017617.3 A2356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr9:139391122 G>A maps to NM_017617.3 A2356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chrX:18956825 G>T maps to NM_000292.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chrX:18956825 G>T maps to NM_000292.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chrX:70514196 C>T maps to NM_007363.4 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chrX:70514196 C>T maps to NM_007363.4 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chrX:119005249 C>T maps to NM_006978.2 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chrX:119005249 C>T maps to NM_006978.2 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chrX:130410217 G>A maps to NM_001170961.1 F876F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chrX:130410217 G>A maps to NM_001170961.1 F876F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chrX:151366157 G>C maps to NM_000808.3 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chrX:151366157 G>C maps to NM_000808.3 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr1:11718435 C>T maps to NM_033182.5 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr1:11718435 C>T maps to NM_033182.5 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr1:65332749 C>T maps to NM_002227.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr1:65332749 C>T maps to NM_002227.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr1:152188506 A>T maps to NM_001009931.1 G1866G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr1:152188506 A>T maps to NM_001009931.1 G1866G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr1:155152366 C>T maps to NM_025058.3 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr1:155152366 C>T maps to NM_025058.3 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr1:200183317 C>T maps to NM_001105517.1 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr1:200183317 C>T maps to NM_001105517.1 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr10:88277385 T>C maps to ENST00000342368 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr10:88277385 T>C maps to ENST00000342368 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr10:135015083 C>T maps to ENST00000368572 D1025D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr10:135015083 C>T maps to ENST00000368572 D1025D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr15:41191579 C>G maps to NM_020857.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr15:41191579 C>G maps to NM_020857.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr15:43816967 C>A maps to ENST00000382031 V1337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr15:43816967 C>A maps to ENST00000382031 V1337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr17:18057107 G>A maps to ENST00000205890 L2662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr17:18057107 G>A maps to ENST00000205890 L2662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr17:80045300 C>T maps to NM_004104.4 S1041S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr17:80045300 C>T maps to NM_004104.4 S1041S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr18:11893496 G>T maps to ENST00000344987 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr18:11893496 G>T maps to ENST00000344987 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr19:47137456 G>T maps to NM_033258.1 S30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr19:47137456 G>T maps to NM_033258.1 S30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr3:121208234 A>G maps to ENST00000393672 N1317N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr3:121208234 A>G maps to ENST00000393672 N1317N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr4:190905408 C>T did not map to a codon.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr4:190905408 C>T did not map to a codon.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr5:141325323 C>T maps to NM_016580.2 A1059A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr5:141325323 C>T maps to NM_016580.2 A1059A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr6:55223937 T>C did not map to a codon.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr6:55223937 T>C did not map to a codon.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr6:117128261 C>G maps to NM_148963.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr6:117128261 C>G maps to NM_148963.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr8:143695620 G>A maps to NM_015193.3 D4D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr8:143695620 G>A maps to NM_015193.3 D4D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr9:133805082 G>A maps to NM_001145106.1 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6482-01A-11D-1870-08 chr9:133805082 G>A maps to NM_001145106.1 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr1:32678153 T>C maps to NM_001099434.1 Y197Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr1:32678153 T>C maps to NM_001099434.1 Y197Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr1:78470769 C>G did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr1:78470769 C>G did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr1:103364317 A>G maps to NM_080629.2 G1396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr1:103364317 A>G maps to NM_080629.2 G1396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr1:120462867 C>G maps to NM_024408.2 V1821V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr1:120462867 C>G maps to NM_024408.2 V1821V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr1:151234660 G>A maps to ENST00000368881 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr1:151234660 G>A maps to ENST00000368881 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr1:183209188 G>A maps to NM_005562.2 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr1:183209188 G>A maps to NM_005562.2 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr1:213414695 C>A maps to NM_012424.3 S626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr1:213414695 C>A maps to NM_012424.3 S626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr10:116057053 C>G maps to NM_001001936.1 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr10:116057053 C>G maps to NM_001001936.1 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr10:127429585 C>G maps to ENST00000356792 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr10:127429585 C>G maps to ENST00000356792 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:799972 G>C maps to NM_145886.3 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:799972 G>C maps to NM_145886.3 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:1629199 G>C maps to ENST00000359229 S209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:1629199 G>C maps to ENST00000359229 S209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:5988968 G>C maps to NM_001146033.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:5988968 G>C maps to NM_001146033.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:58920370 G>A maps to NM_198847.2 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:58920370 G>A maps to NM_198847.2 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:65810463 G>A maps to NM_033036.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:65810463 G>A maps to NM_033036.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:67191489 G>C maps to NM_001166222.1 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:67191489 G>C maps to NM_001166222.1 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:70218612 G>C maps to NM_003626.2 L1024L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:70218612 G>C maps to NM_003626.2 L1024L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:73074383 G>C maps to NM_014786.3 G1710G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:73074383 G>C maps to NM_014786.3 G1710G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:111844774 C>T maps to NM_001037954.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:111844774 C>T maps to NM_001037954.2 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:128781746 C>G maps to NM_000890.3 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr11:128781746 C>G maps to NM_000890.3 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr12:4919507 C>T maps to NM_002235.3 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr12:4919507 C>T maps to NM_002235.3 Q101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr12:12274060 C>G maps to NM_002336.2 *1614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr12:12274060 C>G maps to NM_002336.2 *1614S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CR-6484-01A-11D-1870-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr12:49462887 C>T maps to NM_144593.1 G18G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CR-6484-01A-11D-1870-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr12:49462887 C>T maps to NM_144593.1 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr12:51138606 G>A maps to NM_173602.2 V1572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr12:51138606 G>A maps to NM_173602.2 V1572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr12:52448879 G>C maps to ENST00000360284 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr12:52448879 G>C maps to ENST00000360284 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr12:53709521 G>C maps to NM_015665.5 S99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr12:53709521 G>C maps to NM_015665.5 S99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr12:56548974 G>A maps to NM_002475.4 K113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr12:56548974 G>A maps to NM_002475.4 K113K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr13:22113513 G>A maps to NM_152726.2 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr13:22113513 G>A maps to NM_152726.2 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr13:23913991 G>C maps to NM_014363.4 L1341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr13:23913991 G>C maps to NM_014363.4 L1341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr13:42352180 C>T maps to NM_015058.1 V763V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr13:42352180 C>T maps to NM_015058.1 V763V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr13:47303004 C>T maps to NM_001164211.1 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr13:47303004 C>T maps to NM_001164211.1 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr13:53603066 C>G maps to NM_006418.3 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr13:53603066 C>G maps to NM_006418.3 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr14:51102086 C>T maps to NM_021818.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr14:51102086 C>T maps to NM_021818.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr14:75200789 C>T maps to NM_015962.4 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr14:75200789 C>T maps to NM_015962.4 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr14:100363568 G>A maps to NM_001008707.1 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr14:100363568 G>A maps to NM_001008707.1 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:40565874 G>T maps to NM_020168.4 E581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:40565874 G>T maps to NM_020168.4 E581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:41624609 G>C maps to NM_007280.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:41624609 G>C maps to NM_007280.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:41804372 G>C maps to NM_002344.5 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:41804372 G>C maps to NM_002344.5 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:55838570 G>A maps to NM_015617.1 Q304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:55838570 G>A maps to NM_015617.1 Q304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:62993360 T>C maps to NM_015059.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:62993360 T>C maps to NM_015059.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:65350895 G>A maps to NM_016563.2 Y98Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:65350895 G>A maps to NM_016563.2 Y98Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:74967309 G>A maps to NM_025083.3 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:74967309 G>A maps to NM_025083.3 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:82336880 G>C maps to NM_032246.3 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:82336880 G>C maps to NM_032246.3 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:89738456 G>C did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:89738456 G>C did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:90210982 C>T maps to NM_002666.4 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr15:90210982 C>T maps to NM_002666.4 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr16:1621493 C>T maps to NM_014714.3 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr16:1621493 C>T maps to NM_014714.3 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr16:19126187 C>A maps to NM_001034841.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr16:19126187 C>A maps to NM_001034841.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr16:30904176 G>A maps to NM_004765.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr16:30904176 G>A maps to NM_004765.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr17:5012862 C>T maps to NM_014519.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr17:5012862 C>T maps to NM_014519.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr17:7216602 G>C maps to NM_004489.4 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr17:7216602 G>C maps to NM_004489.4 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr17:28530256 G>T maps to ENST00000394821 S626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr17:28530256 G>T maps to ENST00000394821 S626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr17:39019595 C>T did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr17:39019595 C>T did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr17:76989754 G>C maps to NM_138793.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr17:76989754 G>C maps to NM_138793.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:2444430 C>G maps to NM_032737.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:2444430 C>G maps to NM_032737.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:10080262 G>A maps to NM_015719.3 I1362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:10080262 G>A maps to NM_015719.3 I1362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:11333758 G>C maps to ENST00000319867 L993L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:11333758 G>C maps to ENST00000319867 L993L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:14627499 T>C maps to NM_006145.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:14627499 T>C maps to NM_006145.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:16614077 C>G maps to NM_032207.2 S321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:16614077 C>G maps to NM_032207.2 S321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:20229331 G>A maps to NM_007138.1 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:20229331 G>A maps to NM_007138.1 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:23927131 G>C maps to NM_138286.2 S407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:23927131 G>C maps to NM_138286.2 S407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:34912555 C>G maps to NM_032346.1 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:34912555 C>G maps to NM_032346.1 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:50394715 G>C maps to NM_172374.1 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:50394715 G>C maps to NM_172374.1 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:52519443 G>A maps to NM_025040.3 C469C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:52519443 G>A maps to NM_025040.3 C469C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:54758763 G>A maps to NM_001081442.1 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:54758763 G>A maps to NM_001081442.1 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:55824271 G>A maps to NM_001085488.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:55824271 G>A maps to NM_001085488.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:56423844 C>T maps to NM_176810.2 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr19:56423844 C>T maps to NM_176810.2 Q446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:27695134 G>A maps to NM_015662.1 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:27695134 G>A maps to NM_015662.1 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:32289082 C>T maps to NM_014946.3 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:32289082 C>T maps to NM_014946.3 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:71189954 C>T maps to NM_001692.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:71189954 C>T maps to NM_001692.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:112994206 G>A maps to NM_032494.2 R146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:112994206 G>A maps to NM_032494.2 R146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:179417225 G>C maps to NM_133378.4 S27566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:179417225 G>C maps to NM_133378.4 S27566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:192225421 C>T maps to NM_001130158.1 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:192225421 C>T maps to NM_001130158.1 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:232146797 G>A maps to ENST00000359743 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr2:232146797 G>A maps to ENST00000359743 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr20:3944598 G>A maps to NM_001134338.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr20:3944598 G>A maps to NM_001134338.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr20:23546667 C>G maps to NM_080610.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr20:23546667 C>G maps to NM_080610.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr20:62172622 G>C maps to NM_080823.2 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr20:62172622 G>C maps to NM_080823.2 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr21:30318478 G>A maps to NM_015565.2 F1252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr21:30318478 G>A maps to NM_015565.2 F1252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr22:19384357 C>T maps to NM_003325.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr22:19384357 C>T maps to NM_003325.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr3:122090638 G>C maps to NM_001017928.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr3:122090638 G>C maps to NM_001017928.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr3:142681167 G>C maps to NM_198504.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr3:142681167 G>C maps to NM_198504.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr3:146307602 T>A did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr3:146307602 T>A did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr3:149039270 G>A maps to NM_138786.3 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr3:149039270 G>A maps to NM_138786.3 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr3:157160248 C>T maps to NM_002852.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr3:157160248 C>T maps to NM_002852.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr4:40245287 G>A maps to NM_004310.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr4:40245287 G>A maps to NM_004310.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr5:35806815 C>G maps to NM_024867.3 S1673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr5:35806815 C>G maps to NM_024867.3 S1673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr5:176519744 C>T maps to NM_213647.1 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr5:176519744 C>T maps to NM_213647.1 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr5:176794746 G>A maps to ENST00000398128 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr5:176794746 G>A maps to ENST00000398128 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr6:57015614 C>T maps to NM_001031623.2 L903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr6:57015614 C>T maps to NM_001031623.2 L903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr6:97247015 G>A maps to NM_030784.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr6:97247015 G>A maps to NM_030784.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr6:112537670 C>T did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr6:112537670 C>T did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:1477793 C>T maps to NM_182924.3 R750R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:1477793 C>T maps to NM_182924.3 R750R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:4722412 C>T maps to NM_001037165.1 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:4722412 C>T maps to NM_001037165.1 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:33066515 G>A maps to NM_001002010.1 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:33066515 G>A maps to NM_001002010.1 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:37172812 G>A maps to NM_014800.9 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:37172812 G>A maps to NM_014800.9 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:75643193 G>A maps to NM_016086.2 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:75643193 G>A maps to NM_016086.2 Q107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:92731897 T>C maps to NM_017654.3 E1171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:92731897 T>C maps to NM_017654.3 E1171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:100229800 G>A maps to NM_003227.3 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr7:100229800 G>A maps to NM_003227.3 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr8:61736505 C>T maps to NM_017780.2 V1103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr8:61736505 C>T maps to NM_017780.2 V1103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr8:88885716 C>T maps to NM_152418.3 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr8:88885716 C>T maps to NM_152418.3 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr8:139890086 G>A maps to NM_152888.1 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr8:139890086 G>A maps to NM_152888.1 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr8:144124444 C>G maps to NM_173687.2 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr8:144124444 C>G maps to NM_173687.2 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr9:214661 G>A maps to NM_152569.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr9:214661 G>A maps to NM_152569.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr9:37512609 C>T maps to NM_012166.2 T935T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr9:37512609 C>T maps to NM_012166.2 T935T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr9:140099677 G>A maps to NM_053045.1 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr9:140099677 G>A maps to NM_053045.1 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr1:35223200 C>T maps to NM_005268.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr1:35223200 C>T maps to NM_005268.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr1:94505665 C>T maps to NM_000350.2 S1180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr1:94505665 C>T maps to NM_000350.2 S1180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr1:117984890 C>G maps to NM_006699.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr1:117984890 C>G maps to NM_006699.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr1:180240978 C>T maps to NM_033343.3 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr1:180240978 C>T maps to NM_033343.3 Q206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr1:228476581 C>T maps to NM_001098623.1 T3444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr1:228476581 C>T maps to NM_001098623.1 T3444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr10:43606743 G>A maps to NM_020975.4 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr10:43606743 G>A maps to NM_020975.4 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr10:79760813 C>A maps to NM_007055.3 G800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr10:79760813 C>A maps to NM_007055.3 G800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr10:103339235 G>A maps to NM_013274.3 R568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr10:103339235 G>A maps to NM_013274.3 R568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr11:12345522 A>G did not map to a codon.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr11:12345522 A>G did not map to a codon.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr11:17140214 G>T maps to NM_002645.2 I1004I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr11:17140214 G>T maps to NM_002645.2 I1004I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr11:55594820 C>T maps to NM_001004739.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr11:55594820 C>T maps to NM_001004739.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr11:123676379 G>A maps to NM_001005325.1 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr11:123676379 G>A maps to NM_001005325.1 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr12:49438594 G>C maps to NM_003482.3 S1632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr12:49438594 G>C maps to NM_003482.3 S1632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr12:120510421 C>T maps to NM_207311.2 D399D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr12:120510421 C>T maps to NM_207311.2 D399D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr13:48954378 T>G did not map to a codon.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr13:48954378 T>G did not map to a codon.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr14:68252947 G>A maps to NM_015346.3 R1008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr14:68252947 G>A maps to NM_015346.3 R1008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr14:71493535 C>T maps to NM_014982.2 Q1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr14:71493535 C>T maps to NM_014982.2 Q1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr14:90433739 C>T maps to NM_018319.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr14:90433739 C>T maps to NM_018319.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr14:96783565 G>A maps to NM_018036.5 D1042D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr14:96783565 G>A maps to NM_018036.5 D1042D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr15:58925415 A>G maps to NM_001110.2 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr15:58925415 A>G maps to NM_001110.2 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr16:2816181 C>T maps to NM_016333.3 R1885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr16:2816181 C>T maps to NM_016333.3 R1885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr17:4688866 G>A maps to NM_182566.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr17:4688866 G>A maps to NM_182566.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr17:33288391 G>C maps to NM_006584.3 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr17:33288391 G>C maps to NM_006584.3 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr17:62238186 C>T maps to NM_018469.3 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr17:62238186 C>T maps to NM_018469.3 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr2:140992402 C>T maps to NM_018557.2 A4537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr2:140992402 C>T maps to NM_018557.2 A4537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr2:219559300 C>T maps to NM_015690.3 D818D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr2:219559300 C>T maps to NM_015690.3 D818D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr2:234775834 C>G did not map to a codon.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr2:234775834 C>G did not map to a codon.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr21:34823151 A>G maps to NM_006134.5 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr21:34823151 A>G maps to NM_006134.5 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr21:41725413 C>T maps to NM_001389.3 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr21:41725413 C>T maps to NM_001389.3 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr21:43221623 C>A maps to NM_022115.3 E1434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr21:43221623 C>A maps to NM_022115.3 E1434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr22:41531854 C>T maps to NM_001429.3 Q523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr22:41531854 C>T maps to NM_001429.3 Q523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr3:121649689 T>C maps to NM_021082.3 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr3:121649689 T>C maps to NM_021082.3 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr3:167543054 C>T maps to NM_005025.4 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr3:167543054 C>T maps to NM_005025.4 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr3:193166023 G>C maps to NM_032279.2 S708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr3:193166023 G>C maps to NM_032279.2 S708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr3:197241273 G>A maps to NM_203315.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr3:197241273 G>A maps to NM_203315.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr4:44449817 G>A maps to NM_198353.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr4:44449817 G>A maps to NM_198353.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr4:146467853 G>A did not map to a codon.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr4:146467853 G>A did not map to a codon.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr5:139918551 C>T maps to ENST00000253810 Q2502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr5:139918551 C>T maps to ENST00000253810 Q2502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr5:140903713 A>G maps to ENST00000398557 R1219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr5:140903713 A>G maps to ENST00000398557 R1219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr6:4998959 C>T maps to NM_006638.2 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr6:4998959 C>T maps to NM_006638.2 W183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr6:7229768 G>A maps to NM_001003699.3 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr6:7229768 G>A maps to NM_001003699.3 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr8:22106635 C>T maps to NM_001722.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr8:22106635 C>T maps to NM_001722.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr8:55542591 T>C maps to NM_006269.1 N2050N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr8:55542591 T>C maps to NM_006269.1 N2050N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr9:108151335 G>C maps to NM_080546.3 *658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr9:108151335 G>C maps to NM_080546.3 *658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chrX:53426516 G>A maps to NM_006306.2 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chrX:53426516 G>A maps to NM_006306.2 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chrX:129272622 C>T maps to NM_004208.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chrX:129272622 C>T maps to NM_004208.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr1:40703343 G>A maps to NM_012421.3 T990T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr1:40703343 G>A maps to NM_012421.3 T990T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr1:186072799 G>A maps to NM_031935.2 Q3590Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr1:186072799 G>A maps to NM_031935.2 Q3590Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr11:7689763 C>A maps to NM_016229.3 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr11:7689763 C>A maps to NM_016229.3 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr16:29891362 G>A maps to NM_201575.2 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr16:29891362 G>A maps to NM_201575.2 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr16:70404239 C>T maps to NM_018332.3 R379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr16:70404239 C>T maps to NM_018332.3 R379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr17:34935801 C>T maps to NM_024835.3 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr17:34935801 C>T maps to NM_024835.3 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr18:2923795 T>A maps to NM_014646.2 A717A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr18:2923795 T>A maps to NM_014646.2 A717A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr19:6004276 T>A maps to NM_000635.3 K479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr19:6004276 T>A maps to NM_000635.3 K479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr19:19655207 G>A maps to NM_153221.2 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr19:19655207 G>A maps to NM_153221.2 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr22:17578690 C>T maps to NM_014339.5 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr22:17578690 C>T maps to NM_014339.5 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr4:113353309 C>T maps to NM_025144.3 H869H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr4:113353309 C>T maps to NM_025144.3 H869H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr4:139966006 A>C maps to NM_012118.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr4:139966006 A>C maps to NM_012118.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr5:140741081 C>T maps to NM_018923.2 H460H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr5:140741081 C>T maps to NM_018923.2 H460H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr5:141316761 G>T did not map to a codon.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr5:141316761 G>T did not map to a codon.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr7:123101542 A>T maps to NM_178827.4 C625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chr7:123101542 A>T maps to NM_178827.4 C625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chrX:26157440 G>A maps to NM_173699.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chrX:26157440 G>A maps to NM_173699.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chrX:65413377 C>T maps to NM_138737.3 R477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6488-01A-12D-2078-08 chrX:65413377 C>T maps to NM_138737.3 R477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr1:6314149 G>A maps to NM_207370.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr1:6314149 G>A maps to NM_207370.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr1:12062112 G>A maps to NM_014874.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr1:12062112 G>A maps to NM_014874.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr1:16355703 C>T maps to NM_004070.3 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr1:16355703 C>T maps to NM_004070.3 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr1:44595383 C>T maps to NM_173484.3 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr1:44595383 C>T maps to NM_173484.3 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr1:75072530 C>A maps to NM_001002912.4 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr1:75072530 C>A maps to NM_001002912.4 E415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr1:160312933 G>A maps to NM_001098398.1 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr1:160312933 G>A maps to NM_001098398.1 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr10:11994185 A>G maps to NM_015542.2 D971D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr10:11994185 A>G maps to NM_015542.2 D971D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr10:12238300 A>T maps to NM_006023.2 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr10:12238300 A>T maps to NM_006023.2 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr10:28872435 T>G did not map to a codon.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr10:28872435 T>G did not map to a codon.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr10:82269157 C>T maps to NM_030927.2 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr10:82269157 C>T maps to NM_030927.2 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr10:99123619 G>A maps to NM_015179.3 I1186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr10:99123619 G>A maps to NM_015179.3 I1186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr10:100503693 G>A maps to NM_021828.4 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr10:100503693 G>A maps to NM_021828.4 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr10:127677182 G>A maps to ENST00000368692 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr10:127677182 G>A maps to ENST00000368692 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr11:10825923 C>A maps to ENST00000429377 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr11:10825923 C>A maps to ENST00000429377 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr12:336789 G>A maps to NM_016615.3 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr12:336789 G>A maps to NM_016615.3 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr12:7086774 A>T maps to NM_005768.5 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr12:7086774 A>T maps to NM_005768.5 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr12:51773259 G>A maps to NM_007210.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr12:51773259 G>A maps to NM_007210.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr12:129360458 G>A maps to ENST00000442111 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr12:129360458 G>A maps to ENST00000442111 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr13:52536025 C>T maps to NM_000053.2 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr13:52536025 C>T maps to NM_000053.2 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr13:101287319 C>T maps to NM_032813.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr13:101287319 C>T maps to NM_032813.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr14:23451168 G>A maps to NM_032876.4 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr14:23451168 G>A maps to NM_032876.4 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr15:53889438 C>T maps to NM_182758.2 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr15:53889438 C>T maps to NM_182758.2 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr16:20781490 C>T maps to NM_005622.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr16:20781490 C>T maps to NM_005622.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr16:20927014 G>A maps to NM_020424.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr16:20927014 G>A maps to NM_020424.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr16:27476144 G>A maps to NM_001520.3 Q1790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr16:27476144 G>A maps to NM_001520.3 Q1790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr16:75564111 G>A maps to NM_024533.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr16:75564111 G>A maps to NM_024533.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr17:11648368 A>T maps to NM_001372.3 K2123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr17:11648368 A>T maps to NM_001372.3 K2123*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CR-6491-01A-11D-1870-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-CR-6491-01A-11D-1870-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr17:33521248 G>A maps to NM_152462.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr17:33521248 G>A maps to NM_152462.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr17:37008938 C>T maps to NM_000978.3 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr17:37008938 C>T maps to NM_000978.3 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr17:43227081 G>A maps to NM_006460.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr17:43227081 G>A maps to NM_006460.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr17:46196401 G>A maps to NM_152244.1 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr17:46196401 G>A maps to NM_152244.1 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr18:33706964 C>T maps to NM_012319.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr18:33706964 C>T maps to NM_012319.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr19:10127886 G>A maps to NM_015725.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr19:10127886 G>A maps to NM_015725.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr19:30496289 C>T maps to NM_003796.2 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr19:30496289 C>T maps to NM_003796.2 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr19:37643885 T>C maps to ENST00000356958 K305K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr19:37643885 T>C maps to ENST00000356958 K305K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr19:42720874 G>A maps to NM_133328.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr19:42720874 G>A maps to NM_133328.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr19:47996259 C>T maps to NM_003827.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr19:47996259 C>T maps to NM_003827.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr2:219540847 C>T maps to NM_015690.3 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr2:219540847 C>T maps to NM_015690.3 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr22:23523320 C>T maps to NM_004327.3 Y58Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr22:23523320 C>T maps to NM_004327.3 Y58Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr3:58104675 G>T maps to NM_001164317.1 P941P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr3:58104675 G>T maps to NM_001164317.1 P941P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr3:122145936 G>A maps to NM_002264.3 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr3:122145936 G>A maps to NM_002264.3 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr3:148458872 T>C maps to NM_032049.2 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr3:148458872 T>C maps to NM_032049.2 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr4:3101072 G>A maps to NM_002111.6 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr4:3101072 G>A maps to NM_002111.6 E140E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr4:55594177 G>T maps to NM_000222.2 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr4:55594177 G>T maps to NM_000222.2 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr4:120221570 G>A maps to NM_001170330.1 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr4:120221570 G>A maps to NM_001170330.1 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr5:1219623 C>T maps to NM_001003841.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr5:1219623 C>T maps to NM_001003841.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr5:146778659 G>T maps to NM_001197294.1 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr5:146778659 G>T maps to NM_001197294.1 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr6:33400551 C>T maps to NM_006772.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr6:33400551 C>T maps to NM_006772.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr6:43406407 C>T maps to NM_033450.2 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr6:43406407 C>T maps to NM_033450.2 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr6:73904677 C>T maps to NM_001160133.1 V799V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr6:73904677 C>T maps to NM_001160133.1 V799V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr6:152639351 A>T maps to NM_182961.2 L5479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr6:152639351 A>T maps to NM_182961.2 L5479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr7:44187277 G>A maps to NM_000162.3 D278D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr7:44187277 G>A maps to NM_000162.3 D278D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr7:72856542 G>A maps to NM_032408.3 R1479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr7:72856542 G>A maps to NM_032408.3 R1479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr7:115892373 G>A maps to NM_015641.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr7:115892373 G>A maps to NM_015641.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr8:27964291 T>C maps to NM_018091.5 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr8:27964291 T>C maps to NM_018091.5 N107N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr9:21350757 T>C maps to NM_021002.2 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr9:21350757 T>C maps to NM_021002.2 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr9:128723126 C>T maps to ENST00000373487 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr9:128723126 C>T maps to ENST00000373487 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chrX:153248202 G>A maps to NM_003492.2 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chrX:153248202 G>A maps to NM_003492.2 K230K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr1:109806317 C>T maps to NM_001408.2 L1640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr1:109806317 C>T maps to NM_001408.2 L1640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr1:145765383 T>C maps to NM_001097612.1 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr1:145765383 T>C maps to NM_001097612.1 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr1:231061287 G>A maps to NM_024525.4 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr1:231061287 G>A maps to NM_024525.4 F521F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr11:64802350 C>T maps to NM_013306.4 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr11:64802350 C>T maps to NM_013306.4 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr12:47472578 C>T maps to NM_001143668.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr12:47472578 C>T maps to NM_001143668.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr12:53455638 G>A maps to NM_170754.2 L1163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr12:53455638 G>A maps to NM_170754.2 L1163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr12:110574582 A>G maps to NM_014055.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr12:110574582 A>G maps to NM_014055.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr15:62942334 G>A maps to NM_015059.2 W63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr15:62942334 G>A maps to NM_015059.2 W63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr16:3736065 G>A maps to NM_016292.2 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr16:3736065 G>A maps to NM_016292.2 D134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr17:10209913 T>C maps to NM_003802.2 E1776E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr17:10209913 T>C maps to NM_003802.2 E1776E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr2:203420619 T>G maps to NM_001204.6 P744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr2:203420619 T>G maps to NM_001204.6 P744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr21:46193488 G>A maps to NM_003343.4 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr21:46193488 G>A maps to NM_003343.4 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr21:46875806 C>T maps to ENST00000359759 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr21:46875806 C>T maps to ENST00000359759 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr22:19839544 A>T maps to NM_024627.5 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr22:19839544 A>T maps to NM_024627.5 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr3:140277532 G>C maps to NM_022131.2 V625V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr3:140277532 G>C maps to NM_022131.2 V625V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr4:187530344 G>A maps to ENST00000260147 R3403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr4:187530344 G>A maps to ENST00000260147 R3403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr5:82948497 G>T maps to NM_001884.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr5:82948497 G>T maps to NM_001884.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr5:86659188 T>A maps to NM_002890.1 L493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr5:86659188 T>A maps to NM_002890.1 L493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr5:154393631 G>A maps to NM_001099293.1 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr5:154393631 G>A maps to NM_001099293.1 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr6:24523068 C>T maps to NM_170740.1 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr6:24523068 C>T maps to NM_170740.1 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr6:28327419 G>A maps to NM_024493.2 Q19Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr6:28327419 G>A maps to NM_024493.2 Q19Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr9:139906445 G>A maps to ENST00000355090 I1825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr9:139906445 G>A maps to ENST00000355090 I1825I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chrX:49032202 G>T maps to NM_006150.3 S556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chrX:49032202 G>T maps to NM_006150.3 S556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chrX:153215721 G>C maps to ENST00000369984 G2037G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chrX:153215721 G>C maps to ENST00000369984 G2037G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr12:57988993 C>T maps to NM_024779.4 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr12:57988993 C>T maps to NM_024779.4 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr14:74004391 C>T maps to NM_001037161.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr14:74004391 C>T maps to NM_001037161.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr2:211441129 T>C maps to NM_001122633.1 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr2:211441129 T>C maps to NM_001122633.1 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr6:86197161 C>T maps to NM_002526.2 C353C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr6:86197161 C>T maps to NM_002526.2 C353C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr7:20825288 G>A maps to NM_182700.4 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr7:20825288 G>A maps to NM_182700.4 H49H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr9:114886702 G>A maps to NM_022486.3 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr9:114886702 G>A maps to NM_022486.3 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr9:125288893 G>A maps to ENST00000359439 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr9:125288893 G>A maps to ENST00000359439 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr9:139273677 C>A maps to NM_003086.2 A867A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chr9:139273677 C>A maps to NM_003086.2 A867A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chrX:63412938 T>C maps to NM_152424.3 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6493-01A-11D-1870-08 chrX:63412938 T>C maps to NM_152424.3 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:16914292 C>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:16914292 C>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:55545228 C>A maps to NM_015306.2 G2394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:55545228 C>A maps to NM_015306.2 G2394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:57420404 G>A maps to NM_000066.2 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:57420404 G>A maps to NM_000066.2 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:76877997 G>A maps to NM_152996.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:76877997 G>A maps to NM_152996.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:77763625 G>A maps to NM_174858.1 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:77763625 G>A maps to NM_174858.1 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:117487466 C>T maps to NM_020440.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:117487466 C>T maps to NM_020440.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:117560847 C>T maps to NM_004258.3 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:117560847 C>T maps to NM_004258.3 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:118165681 C>T maps to NM_017709.3 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:118165681 C>T maps to NM_017709.3 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:156554970 A>G maps to NM_001105669.2 K468K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:156554970 A>G maps to NM_001105669.2 K468K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:158151870 C>T maps to NM_001766.3 N126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:158151870 C>T maps to NM_001766.3 N126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:169696912 C>A maps to NM_000450.2 G479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:169696912 C>A maps to NM_000450.2 G479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:197070946 T>C maps to NM_018136.4 Q2478Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:197070946 T>C maps to NM_018136.4 Q2478Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:197896917 T>C maps to NM_020204.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:197896917 T>C maps to NM_020204.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:204130516 G>A maps to NM_000537.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:204130516 G>A maps to NM_000537.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:204159794 G>T maps to ENST00000306118 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:204159794 G>T maps to ENST00000306118 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:210415651 A>G maps to NM_019605.3 K347K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:210415651 A>G maps to NM_019605.3 K347K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:237780710 C>A maps to NM_001035.2 V1947V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:237780710 C>A maps to NM_001035.2 V1947V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:237951286 G>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:237951286 G>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:240370892 C>T maps to ENST00000406993 P1070P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr1:240370892 C>T maps to ENST00000406993 P1070P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:27687957 C>A maps to NM_001034842.3 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:27687957 C>A maps to NM_001034842.3 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:27702470 G>A maps to NM_001034842.3 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:27702470 G>A maps to NM_001034842.3 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:81372066 G>T did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:81372066 G>T did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:89264701 G>T maps to NM_004897.4 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:89264701 G>T maps to NM_004897.4 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:100012125 G>A maps to NM_032211.6 D645D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:100012125 G>A maps to NM_032211.6 D645D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:102684053 G>A maps to NM_001136123.1 K432K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:102684053 G>A maps to NM_001136123.1 K432K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:116975563 G>A maps to NM_207303.2 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:116975563 G>A maps to NM_207303.2 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:124672280 T>A maps to NM_001029888.1 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:124672280 T>A maps to NM_001029888.1 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:132965137 T>C maps to NM_174937.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:132965137 T>C maps to NM_174937.3 T289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:135024219 G>T maps to ENST00000368572 T1302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr10:135024219 G>T maps to ENST00000368572 T1302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:4976783 C>A maps to NM_001004748.1 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:4976783 C>A maps to NM_001004748.1 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:5364442 T>A maps to NM_001005567.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:5364442 T>A maps to NM_001005567.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:5474909 C>A maps to NM_001004754.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:5474909 C>A maps to NM_001004754.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:5989133 C>T maps to NM_001146033.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:5989133 C>T maps to NM_001146033.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:27147272 T>A maps to NM_003986.2 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:27147272 T>A maps to NM_003986.2 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:33094116 G>A maps to NM_001145541.1 E475E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:33094116 G>A maps to NM_001145541.1 E475E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:47197399 A>T did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:47197399 A>T did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:55653179 A>T maps to NM_032681.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:55653179 A>T maps to NM_032681.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:57559054 C>G maps to NM_001085458.1 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:57559054 C>G maps to NM_001085458.1 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:65360634 G>C maps to NM_033347.1 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:65360634 G>C maps to NM_033347.1 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:65421989 T>A maps to NM_021975.3 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:65421989 T>A maps to NM_021975.3 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:67926429 C>T maps to NM_017635.3 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:67926429 C>T maps to NM_017635.3 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:85977216 A>T maps to ENST00000351625 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:85977216 A>T maps to ENST00000351625 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:93797617 C>A maps to NM_001098672.1 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:93797617 C>A maps to NM_001098672.1 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:94040452 G>A maps to NM_001080486.1 W150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:94040452 G>A maps to NM_001080486.1 W150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:122709300 G>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:122709300 G>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:123900616 C>T maps to NM_001004464.1 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:123900616 C>T maps to NM_001004464.1 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:124095639 C>T maps to NM_001007249.1 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:124095639 C>T maps to NM_001007249.1 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:132180114 G>A maps to NM_001144058.1 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:132180114 G>A maps to NM_001144058.1 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr12:6940434 G>A maps to NM_014262.3 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr12:6940434 G>A maps to NM_014262.3 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr12:41966993 G>T maps to NM_001164595.1 E805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr12:41966993 G>T maps to NM_001164595.1 E805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr12:111655723 A>T maps to NM_015267.3 K69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr12:111655723 A>T maps to NM_015267.3 K69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr12:119592087 C>A maps to NM_194286.2 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr12:119592087 C>A maps to NM_194286.2 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr13:113887571 G>A maps to NM_001008895.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr13:113887571 G>A maps to NM_001008895.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr14:63453788 C>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr14:63453788 C>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:44921517 G>A maps to NM_025137.3 Q602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:44921517 G>A maps to NM_025137.3 Q602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:57953655 A>G maps to NM_001018090.3 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:57953655 A>G maps to NM_001018090.3 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:65676727 G>T maps to NM_020962.1 A1124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:65676727 G>T maps to NM_020962.1 A1124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:65916537 C>T maps to NM_004727.2 H40H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:65916537 C>T maps to NM_004727.2 H40H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:76254224 A>G maps to NM_138573.3 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:76254224 A>G maps to NM_138573.3 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:86312263 C>A maps to NM_022480.3 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:86312263 C>A maps to NM_022480.3 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:89424726 G>A maps to NM_178232.2 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr15:89424726 G>A maps to NM_178232.2 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr16:2235117 G>T maps to NM_020764.3 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr16:2235117 G>T maps to NM_020764.3 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr16:20430565 G>T maps to NM_017888.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr16:20430565 G>T maps to NM_017888.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr16:50745418 C>T maps to NM_022162.1 Q533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr16:50745418 C>T maps to NM_022162.1 Q533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr17:30692367 A>T maps to ENST00000394679 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr17:30692367 A>T maps to ENST00000394679 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr17:32582400 G>T maps to NM_002982.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr17:32582400 G>T maps to NM_002982.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr17:40368064 G>A maps to NM_012448.3 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr17:40368064 G>A maps to NM_012448.3 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr17:54990923 G>A maps to NM_005082.4 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr17:54990923 G>A maps to NM_005082.4 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr18:5489137 C>T maps to NM_012307.2 Q15Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr18:5489137 C>T maps to NM_012307.2 Q15Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr18:6955458 C>T maps to NM_005559.2 Q2700Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr18:6955458 C>T maps to NM_005559.2 Q2700Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr18:19761484 C>T maps to NM_005257.3 N458N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr18:19761484 C>T maps to NM_005257.3 N458N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr18:70526310 T>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr18:70526310 T>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:4442303 C>T maps to NM_005483.2 G912G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:4442303 C>T maps to NM_005483.2 G912G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:9059668 G>T maps to NM_024690.2 P9259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:9059668 G>T maps to NM_024690.2 P9259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:20002665 G>T maps to NM_021047.2 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:20002665 G>T maps to NM_021047.2 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:22940511 G>T maps to ENST00000397104 Y642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:22940511 G>T maps to ENST00000397104 Y642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:39976375 G>T maps to NM_001001563.1 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:39976375 G>T maps to NM_001001563.1 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:40095318 G>C did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:40095318 G>C did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:40357439 C>A maps to NM_003890.2 V5291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:40357439 C>A maps to NM_003890.2 V5291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:42187950 C>A maps to NM_006890.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:42187950 C>A maps to NM_006890.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:44536051 A>G maps to NM_001129996.1 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:44536051 A>G maps to NM_001129996.1 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:54668179 G>A maps to NM_001145303.1 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:54668179 G>A maps to NM_001145303.1 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:55087019 G>T did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr19:55087019 G>T did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr2:26696030 T>G maps to NM_194248.2 P1234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr2:26696030 T>G maps to NM_194248.2 P1234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr2:61760929 A>G maps to NM_003400.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr2:61760929 A>G maps to NM_003400.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr2:155157933 G>T maps to NM_052917.2 G330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr2:155157933 G>T maps to NM_052917.2 G330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr2:179470317 G>T maps to NM_133378.4 R15334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr2:179470317 G>T maps to NM_133378.4 R15334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr2:182392029 A>G maps to NM_000885.4 V782V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr2:182392029 A>G maps to NM_000885.4 V782V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr2:196749472 A>G maps to NM_018897.2 L1867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr2:196749472 A>G maps to NM_018897.2 L1867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr20:35885220 A>T maps to NM_021081.4 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr20:35885220 A>T maps to NM_021081.4 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr20:44519213 T>C maps to NM_080749.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr20:44519213 T>C maps to NM_080749.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr20:53260097 A>G maps to NM_018431.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr20:53260097 A>G maps to NM_018431.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr21:22746286 A>C maps to NM_004540.2 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr21:22746286 A>C maps to NM_004540.2 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr21:34923210 G>T maps to NM_138927.1 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr21:34923210 G>T maps to NM_138927.1 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr21:47557203 G>A maps to ENST00000397748 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr21:47557203 G>A maps to ENST00000397748 F496F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr22:17601354 G>T maps to NM_031890.3 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr22:17601354 G>T maps to NM_031890.3 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr22:19121855 G>T maps to NM_022719.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr22:19121855 G>T maps to NM_022719.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr22:30951149 G>A maps to NM_004861.1 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr22:30951149 G>A maps to NM_004861.1 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr22:43015835 G>C maps to NM_001171660.1 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr22:43015835 G>C maps to NM_001171660.1 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr22:51018495 C>G maps to NM_005198.4 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr22:51018495 C>G maps to NM_005198.4 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr3:49020699 C>G maps to NM_006321.2 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr3:49020699 C>G maps to NM_006321.2 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr3:52428567 C>A maps to ENST00000273600 R3636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr3:52428567 C>A maps to ENST00000273600 R3636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr3:87018112 C>A maps to NM_016206.2 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr3:87018112 C>A maps to NM_016206.2 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr3:127783840 C>T maps to ENST00000464451 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr3:127783840 C>T maps to ENST00000464451 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr3:147131244 G>T maps to NM_003412.3 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr3:147131244 G>T maps to NM_003412.3 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr3:150659510 G>T maps to NM_001195794.1 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr3:150659510 G>T maps to NM_001195794.1 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:38047457 G>A maps to NM_015173.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:38047457 G>A maps to NM_015173.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:52895088 T>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:52895088 T>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:70513299 C>T maps to ENST00000514019 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:70513299 C>T maps to ENST00000514019 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:86915781 T>C maps to NM_001025616.2 H325H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:86915781 T>C maps to NM_001025616.2 H325H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:110902033 G>A maps to NM_001963.4 K758K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:110902033 G>A maps to NM_001963.4 K758K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:140640737 G>A maps to ENST00000509479 S1052S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:140640737 G>A maps to ENST00000509479 S1052S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:141868812 G>T maps to NM_020724.1 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:141868812 G>T maps to NM_020724.1 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:143130162 C>A maps to NM_003866.2 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:143130162 C>A maps to NM_003866.2 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:154556599 C>T maps to NM_001131007.1 A1478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:154556599 C>T maps to NM_001131007.1 A1478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:175896768 G>T maps to NM_014269.4 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:175896768 G>T maps to NM_014269.4 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:177056353 T>C maps to NM_170710.4 D422D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:177056353 T>C maps to NM_170710.4 D422D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:7521005 C>A maps to NM_020546.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:7521005 C>A maps to NM_020546.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:13786379 G>A maps to NM_001369.2 L2910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:13786379 G>A maps to NM_001369.2 L2910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:39381643 G>T maps to NM_001343.2 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:39381643 G>T maps to NM_001343.2 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:53751685 C>T maps to NM_006308.2 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:53751685 C>T maps to NM_006308.2 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:127782270 C>A maps to NM_001999.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:127782270 C>A maps to NM_001999.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:131409632 C>A maps to NM_000758.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:131409632 C>A maps to NM_000758.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:134345141 C>A maps to NM_178019.2 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:134345141 C>A maps to NM_178019.2 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:150696551 C>T maps to NM_181776.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:150696551 C>T maps to NM_181776.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:176709507 G>T maps to NM_022455.4 E1979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr5:176709507 G>T maps to NM_022455.4 E1979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr6:13053693 G>A maps to NM_030948.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr6:13053693 G>A maps to NM_030948.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr6:26046018 G>T maps to NM_003531.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr6:26046018 G>T maps to NM_003531.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr6:33133581 G>T maps to NM_080680.2 G1498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr6:33133581 G>T maps to NM_080680.2 G1498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr6:90382060 G>C maps to NM_014611.1 S4551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr6:90382060 G>C maps to NM_014611.1 S4551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr6:123687328 T>C did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr6:123687328 T>C did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr6:132270616 G>A maps to NM_001901.2 Y279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr6:132270616 G>A maps to NM_001901.2 Y279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr6:154727610 G>A maps to NM_173515.2 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr6:154727610 G>A maps to NM_173515.2 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr7:1132335 C>T maps to NM_001505.2 Y324Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr7:1132335 C>T maps to NM_001505.2 Y324Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr7:6042082 C>T did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr7:6042082 C>T did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr7:23383460 A>T maps to NM_006547.2 L318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr7:23383460 A>T maps to NM_006547.2 L318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr7:82784849 A>G maps to NM_033026.5 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr7:82784849 A>G maps to NM_033026.5 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr7:103202351 C>T maps to ENST00000428762 G1753G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr7:103202351 C>T maps to ENST00000428762 G1753G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr7:123270162 C>A maps to NM_080928.3 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr7:123270162 C>A maps to NM_080928.3 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr7:148903832 G>T maps to NM_003575.2 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr7:148903832 G>T maps to NM_003575.2 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:444570 C>T maps to NM_175075.3 W45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:444570 C>T maps to NM_175075.3 W45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:27310643 G>A maps to NM_004103.3 G854G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:27310643 G>A maps to NM_004103.3 G854G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:38287449 G>A maps to NM_001174067.1 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:38287449 G>A maps to NM_001174067.1 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:86386584 G>T maps to NM_000067.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:86386584 G>T maps to NM_000067.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:110510776 T>C maps to ENST00000426474 A3562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:110510776 T>C maps to ENST00000426474 A3562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:113249530 G>C maps to NM_198123.1 Y3505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:113249530 G>C maps to NM_198123.1 Y3505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:113277721 G>T maps to NM_198123.1 G3202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:113277721 G>T maps to NM_198123.1 G3202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:113317076 G>A maps to NM_198123.1 S2713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:113317076 G>A maps to NM_198123.1 S2713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:133856459 A>G maps to ENST00000395386 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr8:133856459 A>G maps to ENST00000395386 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr9:738305 C>T maps to NM_015158.2 Q1119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr9:738305 C>T maps to NM_015158.2 Q1119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr9:8340363 G>T maps to NM_002839.3 T1744T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr9:8340363 G>T maps to NM_002839.3 T1744T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr9:84607176 C>T maps to NM_001001670.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr9:84607176 C>T maps to NM_001001670.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr9:100092788 C>T maps to ENST00000375206 Q855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr9:100092788 C>T maps to ENST00000375206 Q855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr9:127253384 G>C maps to NM_004959.4 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr9:127253384 G>C maps to NM_004959.4 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chrX:209701 G>T maps to NM_018390.3 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chrX:209701 G>T maps to NM_018390.3 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chrX:151303999 G>A maps to NM_021048.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chrX:151303999 G>A maps to NM_021048.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:11007908 C>T maps to NM_001170754.1 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:11007908 C>T maps to NM_001170754.1 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:12024726 C>G maps to ENST00000376369 S499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:12024726 C>G maps to ENST00000376369 S499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:40129050 G>C maps to NM_032526.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:40129050 G>C maps to NM_032526.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:55598229 G>C maps to NM_015306.2 L1175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:55598229 G>C maps to NM_015306.2 L1175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:155161970 C>G maps to ENST00000425082 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:155161970 C>G maps to ENST00000425082 V54V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:183816704 A>G maps to NM_015149.3 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:183816704 A>G maps to NM_015149.3 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:214549656 G>A maps to NM_005401.4 R938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:214549656 G>A maps to NM_005401.4 R938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:226465499 G>A maps to ENST00000366807 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:226465499 G>A maps to ENST00000366807 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:248551736 C>A maps to NM_001005471.1 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr1:248551736 C>A maps to NM_001005471.1 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr10:26409612 T>C maps to NM_017433.4 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr10:26409612 T>C maps to NM_017433.4 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr10:82269076 C>T maps to NM_030927.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr10:82269076 C>T maps to NM_030927.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr11:5255268 C>G maps to NM_000519.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr11:5255268 C>G maps to NM_000519.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr11:65793517 G>A maps to NM_053054.3 Y111Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr11:65793517 G>A maps to NM_053054.3 Y111Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr11:125453531 C>A maps to ENST00000278903 S342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr11:125453531 C>A maps to ENST00000278903 S342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr12:120600728 C>T maps to NM_006836.1 K695K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr12:120600728 C>T maps to NM_006836.1 K695K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr12:123061461 C>G maps to NM_014708.4 L869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr12:123061461 C>G maps to NM_014708.4 L869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr13:76381900 A>G maps to ENST00000357063 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr13:76381900 A>G maps to ENST00000357063 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr14:102504834 G>C maps to NM_001376.4 L3649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr14:102504834 G>C maps to NM_001376.4 L3649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr15:43924463 T>C maps to NM_172095.1 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr15:43924463 T>C maps to NM_172095.1 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr16:4664714 C>G maps to NM_145253.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr16:4664714 C>G maps to NM_145253.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr16:81219115 C>A maps to NM_052892.3 E660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr16:81219115 C>A maps to NM_052892.3 E660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr17:3981228 C>T maps to NM_015113.3 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr17:3981228 C>T maps to NM_015113.3 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr17:18151260 C>T maps to NM_002018.2 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr17:18151260 C>T maps to NM_002018.2 L759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr17:36552193 G>A maps to NM_014598.2 Q573Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr17:36552193 G>A maps to NM_014598.2 Q573Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr17:42483419 C>G did not map to a codon.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr17:42483419 C>G did not map to a codon.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr17:55182884 C>A maps to ENST00000427138 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr17:55182884 C>A maps to ENST00000427138 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr18:48584551 C>G maps to NM_005359.5 S242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr18:48584551 C>G maps to NM_005359.5 S242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr19:35790469 C>T maps to NM_002361.3 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr19:35790469 C>T maps to NM_002361.3 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr19:50361358 G>A maps to NM_017432.3 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr19:50361358 G>A maps to NM_017432.3 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr19:50368398 C>T maps to NM_007254.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr19:50368398 C>T maps to NM_007254.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr19:58102360 C>A maps to NM_001010879.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr19:58102360 C>A maps to NM_001010879.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr19:58863921 C>T did not map to a codon.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr19:58863921 C>T did not map to a codon.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr2:69093521 C>T maps to NM_014482.1 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr2:69093521 C>T maps to NM_014482.1 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr2:136579615 C>A maps to NM_002299.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr2:136579615 C>A maps to NM_002299.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr2:190571720 A>G maps to NM_144708.3 Q656Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr2:190571720 A>G maps to NM_144708.3 Q656Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr20:32232450 G>A maps to NM_005093.3 *605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr20:32232450 G>A maps to NM_005093.3 *605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr20:43385613 G>A maps to NM_182970.2 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr20:43385613 G>A maps to NM_182970.2 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr22:39222540 C>T maps to NM_014293.2 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr22:39222540 C>T maps to NM_014293.2 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr4:3021417 C>T maps to NM_182982.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr4:3021417 C>T maps to NM_182982.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr4:4458948 G>T maps to NM_016930.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr4:4458948 G>T maps to NM_016930.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr4:13601054 G>T maps to NM_148894.2 S2490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr4:13601054 G>T maps to NM_148894.2 S2490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr4:70512978 G>A maps to ENST00000514019 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr4:70512978 G>A maps to ENST00000514019 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr4:110866312 A>G maps to NM_001963.4 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr4:110866312 A>G maps to NM_001963.4 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr4:155161883 A>G maps to NM_017639.3 N1933N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr4:155161883 A>G maps to NM_017639.3 N1933N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr5:422959 G>A maps to NM_020731.3 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr5:422959 G>A maps to NM_020731.3 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr5:82834174 G>T maps to NM_004385.4 E1785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr5:82834174 G>T maps to NM_004385.4 E1785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr5:86675621 C>G maps to NM_002890.1 S853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr5:86675621 C>G maps to NM_002890.1 S853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr5:141358011 C>T maps to NM_183399.1 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr5:141358011 C>T maps to NM_183399.1 Q151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr6:30859859 C>G maps to NM_013994.2 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr6:30859859 C>G maps to NM_013994.2 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr6:30860255 C>T maps to NM_013994.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr6:30860255 C>T maps to NM_013994.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr6:30862323 C>G maps to NM_013994.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr6:30862323 C>G maps to NM_013994.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr6:39874210 G>T maps to ENST00000425303 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr6:39874210 G>T maps to ENST00000425303 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr6:151161324 C>T maps to NM_001029884.1 Q1151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr6:151161324 C>T maps to NM_001029884.1 Q1151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr7:25163648 C>T maps to NM_018947.5 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr7:25163648 C>T maps to NM_018947.5 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr8:104343655 C>G maps to NM_003506.3 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr8:104343655 C>G maps to NM_003506.3 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr8:116631734 G>C maps to NM_014112.2 S197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr8:116631734 G>C maps to NM_014112.2 S197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr8:144995408 C>T maps to NM_201380.2 E2997E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr8:144995408 C>T maps to NM_201380.2 E2997E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr8:144996218 C>T maps to NM_201380.2 E2727E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr8:144996218 C>T maps to NM_201380.2 E2727E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr9:32493812 G>A maps to NM_014314.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr9:32493812 G>A maps to NM_014314.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr9:136030584 G>A maps to NM_021996.4 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7365-01A-11D-2012-08 chr9:136030584 G>A maps to NM_021996.4 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr1:6635142 C>T maps to NM_138697.3 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr1:6635142 C>T maps to NM_138697.3 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr1:55282672 T>A maps to NM_001110533.1 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr1:55282672 T>A maps to NM_001110533.1 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr1:57351626 A>T maps to NM_000562.2 K295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr1:57351626 A>T maps to NM_000562.2 K295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr1:227935682 C>T maps to NM_053052.3 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr1:227935682 C>T maps to NM_053052.3 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr1:237659855 G>A maps to NM_001035.2 Q669Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr1:237659855 G>A maps to NM_001035.2 Q669Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr1:248223986 G>T maps to NM_001004687.1 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr1:248223986 G>T maps to NM_001004687.1 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr1:248224180 C>G maps to NM_001004687.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr1:248224180 C>G maps to NM_001004687.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr11:56310670 C>T maps to NM_001005245.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr11:56310670 C>T maps to NM_001005245.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr11:57085294 A>G maps to NM_033396.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr11:57085294 A>G maps to NM_033396.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr11:57582973 T>C did not map to a codon.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr11:57582973 T>C did not map to a codon.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr12:43822058 G>A maps to ENST00000389420 T1310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr12:43822058 G>A maps to ENST00000389420 T1310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr12:66531826 G>A maps to ENST00000286424 Y257Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr12:66531826 G>A maps to ENST00000286424 Y257Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr12:125470689 C>T maps to NM_032656.3 E76E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr12:125470689 C>T maps to NM_032656.3 E76E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr13:77566262 C>T maps to NM_006493.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr13:77566262 C>T maps to NM_006493.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr13:84453688 G>A maps to NM_052910.1 R652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr13:84453688 G>A maps to NM_052910.1 R652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr15:62939592 C>G maps to NM_015059.2 Y28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr15:62939592 C>G maps to NM_015059.2 Y28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr16:2569562 C>T maps to NM_001694.3 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr16:2569562 C>T maps to NM_001694.3 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr16:15127243 G>A maps to NM_015027.2 E600E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr16:15127243 G>A maps to NM_015027.2 E600E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr16:20486733 C>T maps to NM_001010845.2 Y315Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr16:20486733 C>T maps to NM_001010845.2 Y315Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr17:44770321 C>T maps to NM_006178.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr17:44770321 C>T maps to NM_006178.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr17:58009057 G>A maps to NM_003161.2 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr17:58009057 G>A maps to NM_003161.2 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr19:6714451 C>T maps to NM_000064.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr19:6714451 C>T maps to NM_000064.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr19:12256888 C>T maps to ENST00000439556 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr19:12256888 C>T maps to ENST00000439556 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr19:45004352 G>T did not map to a codon.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr19:45004352 G>T did not map to a codon.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr19:50250009 G>A maps to NM_021733.1 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr19:50250009 G>A maps to NM_021733.1 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr19:55494908 G>T maps to NM_017852.3 E615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr19:55494908 G>T maps to NM_017852.3 E615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr2:127451473 C>A maps to NM_002101.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr2:127451473 C>A maps to NM_002101.3 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr2:153504403 C>T maps to NM_052905.3 A1088A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr2:153504403 C>T maps to NM_052905.3 A1088A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr2:183627483 A>C maps to NM_018981.1 R741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr2:183627483 A>C maps to NM_018981.1 R741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr2:202593825 C>T maps to NM_020919.3 K887K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr2:202593825 C>T maps to NM_020919.3 K887K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr20:16721613 G>A maps to NM_198220.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr20:16721613 G>A maps to NM_198220.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr20:40162086 A>G maps to NM_032221.3 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr20:40162086 A>G maps to NM_032221.3 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr22:46859979 G>A maps to NM_014246.1 G1269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr22:46859979 G>A maps to NM_014246.1 G1269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr3:105421036 T>A maps to NM_170662.3 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr3:105421036 T>A maps to NM_170662.3 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr3:120053966 G>A maps to NM_001099678.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr3:120053966 G>A maps to NM_001099678.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr3:126220059 C>T did not map to a codon.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr3:126220059 C>T did not map to a codon.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr3:149216508 G>C maps to NM_004617.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr3:149216508 G>C maps to NM_004617.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr4:72423470 C>T maps to NM_001098484.2 Q936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr4:72423470 C>T maps to NM_001098484.2 Q936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr4:110222986 G>A maps to ENST00000333642 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr4:110222986 G>A maps to ENST00000333642 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr4:155158156 G>A maps to NM_017639.3 F2094F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr4:155158156 G>A maps to NM_017639.3 F2094F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr5:31323024 C>T maps to NM_004932.2 D661D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr5:31323024 C>T maps to NM_004932.2 D661D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr5:38933398 T>C maps to NM_003999.2 S931S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr5:38933398 T>C maps to NM_003999.2 S931S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr5:70898413 G>A maps to NM_022132.4 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr5:70898413 G>A maps to NM_022132.4 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr5:137426350 G>A maps to NM_058244.2 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr5:137426350 G>A maps to NM_058244.2 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr5:140346784 C>G maps to NM_018899.5 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr5:140346784 C>G maps to NM_018899.5 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr6:38831661 G>T maps to ENST00000327475 S2096S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr6:38831661 G>T maps to ENST00000327475 S2096S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr6:56495120 G>T maps to ENST00000361203 L1190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr6:56495120 G>T maps to ENST00000361203 L1190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr7:35930337 C>T maps to NM_001788.4 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr7:35930337 C>T maps to NM_001788.4 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr7:38765890 A>C maps to NM_014396.3 A840A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr7:38765890 A>C maps to NM_014396.3 A840A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr7:86416015 G>A maps to NM_000840.2 W303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr7:86416015 G>A maps to NM_000840.2 W303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr7:138583772 G>A maps to NM_001164665.1 L1259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr7:138583772 G>A maps to NM_001164665.1 L1259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr7:139724437 C>T maps to NM_022750.2 Q676Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr7:139724437 C>T maps to NM_022750.2 Q676Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr7:142612692 G>A maps to NM_019841.4 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr7:142612692 G>A maps to NM_019841.4 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr7:154738230 T>G maps to NM_007349.3 R1042R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr7:154738230 T>G maps to NM_007349.3 R1042R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr8:30977860 G>T maps to NM_000553.4 E851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr8:30977860 G>T maps to NM_000553.4 E851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr9:119976973 C>A maps to ENST00000313400 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr9:119976973 C>A maps to ENST00000313400 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr9:137017112 G>A maps to NM_052821.3 W198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chr9:137017112 G>A maps to NM_052821.3 W198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chrX:103268088 T>C maps to NM_001002916.3 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7367-01A-11D-2012-08 chrX:103268088 T>C maps to NM_001002916.3 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:11249655 C>G maps to NM_021146.2 S7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:11249655 C>G maps to NM_021146.2 S7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:17609456 C>G maps to NM_016233.2 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:17609456 C>G maps to NM_016233.2 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:41235026 G>A did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:41235026 G>A did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:45243772 G>A maps to NM_001012.1 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:45243772 G>A maps to NM_001012.1 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:65858190 G>T maps to ENST00000371069 E516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:65858190 G>T maps to ENST00000371069 E516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:150235225 T>G maps to NM_012113.1 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:150235225 T>G maps to NM_012113.1 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:196658598 G>A maps to NM_000186.3 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:196658598 G>A maps to NM_000186.3 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:242045250 C>T maps to NM_006027.4 Q715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr1:242045250 C>T maps to NM_006027.4 Q715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr10:5956204 C>T maps to NM_032807.3 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr10:5956204 C>T maps to NM_032807.3 Q508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr10:69699407 G>A maps to NM_022079.2 S844S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr10:69699407 G>A maps to NM_022079.2 S844S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr10:112356207 G>A maps to NM_005445.3 R672R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr10:112356207 G>A maps to NM_005445.3 R672R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr10:131641454 C>T maps to ENST00000355311 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr10:131641454 C>T maps to ENST00000355311 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr11:76709866 T>C did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr11:76709866 T>C did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr11:107676146 C>T maps to NM_017515.4 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr11:107676146 C>T maps to NM_017515.4 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr12:25702359 A>T maps to NM_001145728.1 Y70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr12:25702359 A>T maps to NM_001145728.1 Y70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr12:26217551 C>G maps to NM_001164747.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr12:26217551 C>G maps to NM_001164747.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr12:49225033 G>C maps to NM_004818.2 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr12:49225033 G>C maps to NM_004818.2 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr12:120882719 C>T maps to NM_016399.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr12:120882719 C>T maps to NM_016399.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr12:122794384 G>T maps to ENST00000302528 S1173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr12:122794384 G>T maps to ENST00000302528 S1173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr14:93118911 T>A maps to NM_024832.3 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr14:93118911 T>A maps to NM_024832.3 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr15:75105239 C>G maps to NM_021819.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr15:75105239 C>G maps to NM_021819.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr15:75105353 C>T maps to NM_021819.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr15:75105353 C>T maps to NM_021819.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr16:55601231 A>G maps to NM_032330.1 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr16:55601231 A>G maps to NM_032330.1 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr17:7127130 G>A did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr17:7127130 G>A did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr17:8701979 G>A maps to NM_152599.3 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr17:8701979 G>A maps to NM_152599.3 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr17:27442706 C>T maps to NM_078471.3 E734E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr17:27442706 C>T maps to NM_078471.3 E734E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr17:43923105 C>T maps to NM_175882.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr17:43923105 C>T maps to NM_175882.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr18:480722 G>A maps to NM_130386.2 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr18:480722 G>A maps to NM_130386.2 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr18:29104494 C>T maps to NM_001943.3 Q259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr18:29104494 C>T maps to NM_001943.3 Q259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr18:59221720 C>T maps to NM_031891.2 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr18:59221720 C>T maps to NM_031891.2 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr19:4101136 C>G maps to NM_030662.3 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr19:4101136 C>G maps to NM_030662.3 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr19:5754219 G>A maps to NM_152784.3 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr19:5754219 G>A maps to NM_152784.3 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr19:8618293 C>G maps to NM_012335.3 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr19:8618293 C>G maps to NM_012335.3 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr19:40368714 G>A maps to NM_003890.2 G4211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr19:40368714 G>A maps to NM_003890.2 G4211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr19:55559838 G>C maps to NM_001145971.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr19:55559838 G>C maps to NM_001145971.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr2:44079963 C>T maps to NM_022437.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr2:44079963 C>T maps to NM_022437.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr2:113251797 C>G maps to NM_153712.4 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr2:113251797 C>G maps to NM_153712.4 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr2:168103754 T>G maps to NM_152381.5 A1951A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr2:168103754 T>G maps to NM_152381.5 A1951A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr2:189873852 A>G maps to NM_000090.3 G1243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr2:189873852 A>G maps to NM_000090.3 G1243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr2:203157550 C>T maps to NM_015934.3 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr2:203157550 C>T maps to NM_015934.3 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr20:17937597 G>C maps to NM_152227.1 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr20:17937597 G>C maps to NM_152227.1 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr20:25604530 G>A maps to NM_152667.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr20:25604530 G>A maps to NM_152667.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr20:37209994 G>A maps to ENST00000416116 W15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr20:37209994 G>A maps to ENST00000416116 W15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr22:22869588 T>C maps to NM_080740.3 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr22:22869588 T>C maps to NM_080740.3 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr22:38323541 G>A maps to NM_033386.2 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr22:38323541 G>A maps to NM_033386.2 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr22:39497504 C>T maps to NM_001166003.1 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr22:39497504 C>T maps to NM_001166003.1 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr3:1363507 C>G maps to NM_014461.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr3:1363507 C>G maps to NM_014461.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr3:43344764 C>T maps to NM_017719.4 R24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr3:43344764 C>T maps to NM_017719.4 R24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr3:47957726 G>A maps to ENST00000426837 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr3:47957726 G>A maps to ENST00000426837 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr3:130714943 C>T maps to NM_001001486.1 F705F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr3:130714943 C>T maps to NM_001001486.1 F705F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr4:68543385 T>A maps to NM_018227.5 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr4:68543385 T>A maps to NM_018227.5 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:7867641 C>G maps to NM_024091.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:7867641 C>G maps to NM_024091.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:36251469 G>A maps to NM_001161429.1 C458C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:36251469 G>A maps to NM_001161429.1 C458C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:75490759 C>T maps to NM_014979.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:75490759 C>T maps to NM_014979.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:140175901 C>T maps to NM_018905.2 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:140175901 C>T maps to NM_018905.2 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:140768637 C>G maps to NM_003736.2 S396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:140768637 C>G maps to NM_003736.2 S396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:148619422 C>T maps to NM_014945.2 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:148619422 C>T maps to NM_014945.2 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:149516592 C>T maps to NM_002609.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:149516592 C>T maps to NM_002609.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:180472572 C>T maps to NM_152547.4 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr5:180472572 C>T maps to NM_152547.4 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr6:32169063 C>G maps to NM_004557.3 L1323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr6:32169063 C>G maps to NM_004557.3 L1323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr6:41753184 G>C maps to NM_013397.5 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr6:41753184 G>C maps to NM_013397.5 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr6:51890329 C>T maps to NM_138694.3 S1426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr6:51890329 C>T maps to NM_138694.3 S1426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr6:105824003 G>C maps to NM_002726.4 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr6:105824003 G>C maps to NM_002726.4 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr6:114378933 G>A maps to NM_153612.3 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr6:114378933 G>A maps to NM_153612.3 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr8:11172548 C>T maps to NM_015458.3 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr8:11172548 C>T maps to NM_015458.3 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr8:30889926 C>T maps to NM_013357.2 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr8:30889926 C>T maps to NM_013357.2 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr8:57025629 G>A maps to NM_005372.1 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr8:57025629 G>A maps to NM_005372.1 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr9:71606109 G>A maps to NM_003558.2 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chr9:71606109 G>A maps to NM_003558.2 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chrX:1407733 G>A maps to NM_001161530.1 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chrX:1407733 G>A maps to NM_001161530.1 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chrX:15349713 G>A maps to NM_002641.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chrX:15349713 G>A maps to NM_002641.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chrX:19568090 C>T did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chrX:19568090 C>T did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chrX:44870204 G>A did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chrX:44870204 G>A did not map to a codon.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chrX:134426279 C>T maps to NM_007131.3 W177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7368-01A-11D-2129-08 chrX:134426279 C>T maps to NM_007131.3 W177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr1:14075947 C>A maps to NM_012231.4 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr1:14075947 C>A maps to NM_012231.4 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr1:33402523 G>A maps to NM_153341.2 A694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr1:33402523 G>A maps to NM_153341.2 A694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr1:154524643 G>A maps to NM_017582.6 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr1:154524643 G>A maps to NM_017582.6 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr11:2190936 G>A maps to NM_199292.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr11:2190936 G>A maps to NM_199292.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr11:6191144 G>A maps to NM_001004052.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr11:6191144 G>A maps to NM_001004052.1 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr11:26734240 G>A maps to NM_178498.3 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr11:26734240 G>A maps to NM_178498.3 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr14:42360815 A>T maps to NM_152447.3 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr14:42360815 A>T maps to NM_152447.3 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr15:90168260 C>T maps to NM_152259.3 R1574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr15:90168260 C>T maps to NM_152259.3 R1574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr17:78063684 T>G did not map to a codon.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr17:78063684 T>G did not map to a codon.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr19:4267628 G>A maps to NM_018074.4 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr19:4267628 G>A maps to NM_018074.4 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr19:5455921 C>T maps to NM_181710.3 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr19:5455921 C>T maps to NM_181710.3 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr20:31671215 C>A maps to NM_182519.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr20:31671215 C>A maps to NM_182519.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr20:43530338 C>T maps to NM_139323.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr20:43530338 C>T maps to NM_139323.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr22:32009446 G>T maps to NM_001007467.1 T891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr22:32009446 G>T maps to NM_001007467.1 T891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr3:102171892 C>A maps to NM_175056.1 C95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr3:102171892 C>A maps to NM_175056.1 C95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr4:83748770 G>A maps to ENST00000505472 F1045F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr4:83748770 G>A maps to ENST00000505472 F1045F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr4:100131635 G>A maps to NM_001102470.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr4:100131635 G>A maps to NM_001102470.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr5:37008755 T>G maps to NM_133433.3 L1451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr5:37008755 T>G maps to NM_133433.3 L1451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr5:41008748 C>T maps to ENST00000296803 V1190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr5:41008748 C>T maps to ENST00000296803 V1190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr5:112868638 C>T maps to NM_022828.3 Q247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr5:112868638 C>T maps to NM_022828.3 Q247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr6:348126 G>A maps to ENST00000457386 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr6:348126 G>A maps to ENST00000457386 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr6:36824425 T>C maps to NM_016059.4 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr6:36824425 T>C maps to NM_016059.4 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr6:43188999 C>T maps to ENST00000354495 L2231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr6:43188999 C>T maps to ENST00000354495 L2231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr8:145583548 C>T maps to NM_024531.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chr8:145583548 C>T maps to NM_024531.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chrX:139586673 C>T maps to NM_005634.2 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7369-01A-11D-2129-08 chrX:139586673 C>T maps to NM_005634.2 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:17295648 G>T maps to NM_014675.3 L1705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:17295648 G>T maps to NM_014675.3 L1705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:34174730 C>T maps to ENST00000373381 L1138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:34174730 C>T maps to ENST00000373381 L1138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:103462680 C>T did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:103462680 C>T did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:145075790 G>T maps to NM_022359.5 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:145075790 G>T maps to NM_022359.5 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:158435443 C>T maps to NM_001004473.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:158435443 C>T maps to NM_001004473.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:158582606 C>T maps to NM_003126.2 Q2378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:158582606 C>T maps to NM_003126.2 Q2378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:162824617 G>A maps to NM_178550.4 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:162824617 G>A maps to NM_178550.4 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:180006139 G>T maps to NM_014810.4 S1342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:180006139 G>T maps to NM_014810.4 S1342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:181690907 G>A maps to ENST00000357570 E657E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:181690907 G>A maps to ENST00000357570 E657E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:207106356 C>A maps to NM_002644.3 G620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:207106356 C>A maps to NM_002644.3 G620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:209781227 C>A maps to NM_020439.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:209781227 C>A maps to NM_020439.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:210006692 A>G maps to NM_014388.6 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:210006692 A>G maps to NM_014388.6 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:215955410 C>G maps to ENST00000366943 T3571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:215955410 C>G maps to ENST00000366943 T3571T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:231335943 C>T maps to NM_001004342.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:231335943 C>T maps to NM_001004342.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:237817704 G>T maps to NM_001035.2 L2652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:237817704 G>T maps to NM_001035.2 L2652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:248224348 C>T maps to NM_001004687.1 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:248224348 C>T maps to NM_001004687.1 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:248756556 G>A maps to NM_001004693.1 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr1:248756556 G>A maps to NM_001004693.1 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr10:76803729 C>T maps to NM_001003892.1 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr10:76803729 C>T maps to NM_001003892.1 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr10:87614372 C>A did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr10:87614372 C>A did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr10:117885027 C>T maps to NM_005264.4 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr10:117885027 C>T maps to NM_005264.4 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:3249861 G>A maps to ENST00000328215 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:3249861 G>A maps to ENST00000328215 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:4470787 G>T maps to NM_001005172.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:4470787 G>T maps to NM_001005172.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:5373013 G>T maps to NM_001004750.1 G93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:5373013 G>T maps to NM_001004750.1 G93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:5510562 C>A maps to NM_001005163.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:5510562 C>A maps to NM_001005163.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:31484807 G>A maps to NM_144981.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:31484807 G>A maps to NM_144981.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:44286553 C>T maps to NM_021926.3 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:44286553 C>T maps to NM_021926.3 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:47611621 C>T maps to NM_031909.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:47611621 C>T maps to NM_031909.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:48327914 C>A maps to NM_001004725.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:48327914 C>A maps to NM_001004725.1 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:55658942 G>T maps to NM_032681.3 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:55658942 G>T maps to NM_032681.3 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:55944655 C>A maps to NM_001005492.1 S188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:55944655 C>A maps to NM_001005492.1 S188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:57379389 C>A maps to ENST00000403558 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:57379389 C>A maps to ENST00000403558 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:60637114 C>A maps to NM_207341.2 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:60637114 C>A maps to NM_207341.2 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:61094320 T>A maps to NM_001923.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:61094320 T>A maps to NM_001923.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:62296992 T>C maps to NM_001620.1 P1632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:62296992 T>C maps to NM_001620.1 P1632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:67399228 C>G maps to NM_005995.4 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:67399228 C>G maps to NM_005995.4 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:68181316 C>T maps to NM_002335.2 F888F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:68181316 C>T maps to NM_002335.2 F888F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:102738032 G>C maps to ENST00000326227 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:102738032 G>C maps to ENST00000326227 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:119229765 A>T maps to NM_004205.4 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:119229765 A>T maps to NM_004205.4 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:132306620 C>T maps to NM_002545.3 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr11:132306620 C>T maps to NM_002545.3 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:6646844 C>A maps to NM_002046.3 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:6646844 C>A maps to NM_002046.3 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:12232293 C>T maps to NM_138722.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:12232293 C>T maps to NM_138722.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:43769236 A>G maps to ENST00000389420 A1797A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:43769236 A>G maps to ENST00000389420 A1797A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:43847819 C>T maps to ENST00000389420 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:43847819 C>T maps to ENST00000389420 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:53684656 G>T maps to NM_012291.4 L1799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:53684656 G>T maps to NM_012291.4 L1799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:72936126 G>A maps to NM_013381.2 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:72936126 G>A maps to NM_013381.2 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:78400832 G>A maps to NM_014903.4 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:78400832 G>A maps to NM_014903.4 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:82147792 G>T maps to NM_003625.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:82147792 G>T maps to NM_003625.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:88381701 G>A maps to NM_152589.1 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:88381701 G>A maps to NM_152589.1 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:109684048 C>A maps to NM_001093.3 I1789I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:109684048 C>A maps to NM_001093.3 I1789I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:111923528 G>A maps to NM_002973.3 S975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:111923528 G>A maps to NM_002973.3 S975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:120652756 G>T maps to NM_001080855.1 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:120652756 G>T maps to NM_001080855.1 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:123485363 G>A maps to NM_020845.2 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:123485363 G>A maps to NM_020845.2 F395F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:130926459 C>A maps to NM_015347.4 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:130926459 C>A maps to NM_015347.4 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:132510275 G>T maps to ENST00000333577 A1683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:132510275 G>T maps to ENST00000333577 A1683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:133433062 G>C maps to NM_001161344.1 S419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr12:133433062 G>C maps to NM_001161344.1 S419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr13:99092243 G>T maps to NM_005766.2 V821V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr13:99092243 G>T maps to NM_005766.2 V821V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr14:25043922 T>C maps to NM_001911.2 Q99Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr14:25043922 T>C maps to NM_001911.2 Q99Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr14:59112861 A>G maps to NM_016651.5 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr14:59112861 A>G maps to NM_016651.5 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr14:60756618 G>T maps to NM_177952.2 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr14:60756618 G>T maps to NM_177952.2 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr14:63671524 G>A did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr14:63671524 G>A did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr14:100157457 G>T maps to NM_006668.1 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr14:100157457 G>T maps to NM_006668.1 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:23811592 G>T maps to NM_005664.3 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:23811592 G>T maps to NM_005664.3 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:27128608 C>T maps to NM_000810.3 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:27128608 C>T maps to NM_000810.3 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:31197879 G>A maps to NM_014967.4 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:31197879 G>A maps to NM_014967.4 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:34640392 C>T maps to ENST00000438749 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:34640392 C>T maps to ENST00000438749 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:42117603 C>T maps to NM_001128608.1 A1505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:42117603 C>T maps to NM_001128608.1 A1505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:42278075 G>A maps to NM_001080490.1 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:42278075 G>A maps to NM_001080490.1 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:45560573 C>T maps to NM_004212.3 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:45560573 C>T maps to NM_004212.3 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:69347809 C>T maps to NM_024505.3 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:69347809 C>T maps to NM_024505.3 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:76630853 C>A maps to NM_145805.1 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:76630853 C>A maps to NM_145805.1 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:78758819 A>G maps to NM_004136.2 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:78758819 A>G maps to NM_004136.2 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:78765605 A>G maps to NM_004136.2 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:78765605 A>G maps to NM_004136.2 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:85326319 C>T maps to NM_014630.2 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr15:85326319 C>T maps to NM_014630.2 F138F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr16:9923429 G>T maps to NM_000833.3 V619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr16:9923429 G>T maps to NM_000833.3 V619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr16:23647269 A>C maps to NM_024675.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr16:23647269 A>C maps to NM_024675.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr16:30770422 C>T did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr16:30770422 C>T did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr16:31143905 C>T maps to NM_002773.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr16:31143905 C>T maps to NM_002773.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:7366416 C>A maps to NM_020899.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:7366416 C>A maps to NM_020899.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:10364259 C>A maps to NM_017533.2 E374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:10364259 C>A maps to NM_017533.2 E374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:10366497 T>C maps to NM_017533.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:10366497 T>C maps to NM_017533.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:18030102 A>G did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:18030102 A>G did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:21205549 C>A maps to NM_145109.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:21205549 C>A maps to NM_145109.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:33768372 G>A maps to NM_144682.5 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:33768372 G>A maps to NM_144682.5 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:61557821 C>T maps to NM_000789.3 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:61557821 C>T maps to NM_000789.3 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:65628288 A>T maps to NM_012417.2 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:65628288 A>T maps to NM_012417.2 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:65722657 G>A maps to NM_015462.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr17:65722657 G>A maps to NM_015462.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr18:8113616 G>T maps to NM_001105244.1 E664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr18:8113616 G>T maps to NM_001105244.1 E664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr18:11868554 C>T maps to NM_182978.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr18:11868554 C>T maps to NM_182978.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr18:63547682 C>A maps to NM_004361.2 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr18:63547682 C>A maps to NM_004361.2 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:9074422 G>T maps to NM_024690.2 T4341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:9074422 G>T maps to NM_024690.2 T4341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:10505717 C>A maps to NM_007065.3 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:10505717 C>A maps to NM_007065.3 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:15537871 C>A maps to ENST00000389282 P1191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:15537871 C>A maps to ENST00000389282 P1191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:37440566 C>A maps to NM_198539.2 S171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:37440566 C>A maps to NM_198539.2 S171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:42224050 C>T maps to NM_004363.2 D565D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:42224050 C>T maps to NM_004363.2 D565D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:46914603 C>T maps to NM_032040.3 W488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:46914603 C>T maps to NM_032040.3 W488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:50204809 C>A maps to NM_152359.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:50204809 C>A maps to NM_152359.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:50305112 C>T maps to NM_014203.2 I640I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:50305112 C>T maps to NM_014203.2 I640I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:50412134 C>A maps to NM_012346.4 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:50412134 C>A maps to NM_012346.4 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:51633326 C>A maps to NM_014441.2 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:51633326 C>A maps to NM_014441.2 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:54418658 C>A maps to NM_031896.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:54418658 C>A maps to NM_031896.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:56487624 G>T maps to NM_176811.2 L944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:56487624 G>T maps to NM_176811.2 L944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:57931541 A>C maps to NM_006959.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:57931541 A>C maps to NM_006959.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:74763194 T>A maps to NM_032603.2 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:74763194 T>A maps to NM_032603.2 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:95952297 C>A maps to NM_144707.2 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:95952297 C>A maps to NM_144707.2 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:100623730 G>A maps to NM_001025108.1 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:100623730 G>A maps to NM_001025108.1 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:109408220 G>A maps to NM_144978.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:109408220 G>A maps to NM_144978.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:136467632 A>G maps to ENST00000409606 G822G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:136467632 A>G maps to ENST00000409606 G822G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:160257123 G>A maps to NM_013450.2 Q962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:160257123 G>A maps to NM_013450.2 Q962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:179439362 G>T maps to NM_133378.4 T21264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:179439362 G>T maps to NM_133378.4 T21264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:219677073 G>T maps to NM_000784.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:219677073 G>T maps to NM_000784.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:241661289 C>T maps to ENST00000373308 L1567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr2:241661289 C>T maps to ENST00000373308 L1567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr20:947817 C>T maps to NM_001029871.3 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr20:947817 C>T maps to NM_001029871.3 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr20:21687097 C>T maps to NM_006192.3 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr20:21687097 C>T maps to NM_006192.3 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr20:44839175 G>T maps to NM_021248.1 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr20:44839175 G>T maps to NM_021248.1 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr20:60887106 C>T did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr20:60887106 C>T did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr22:46657866 G>C maps to NM_006071.1 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr22:46657866 G>C maps to NM_006071.1 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:38951679 A>T maps to ENST00000302328 Y326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:38951679 A>T maps to ENST00000302328 Y326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:45152274 G>T maps to NM_022842.3 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:45152274 G>T maps to NM_022842.3 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:51982441 C>T maps to NM_001003931.2 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:51982441 C>T maps to NM_001003931.2 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:121352000 C>A maps to NM_005335.4 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:121352000 C>A maps to NM_005335.4 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:137822453 G>A maps to NM_173543.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:137822453 G>A maps to NM_173543.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:145917673 G>A maps to NM_020353.2 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:145917673 G>A maps to NM_020353.2 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:186944201 G>T maps to NM_001879.5 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:186944201 G>T maps to NM_001879.5 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:194149601 C>T maps to NM_024524.3 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:194149601 C>T maps to NM_024524.3 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:194344009 C>A maps to NM_001166305.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:194344009 C>A maps to NM_001166305.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:195479979 G>A maps to NM_018406.5 A5150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr3:195479979 G>A maps to NM_018406.5 A5150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr4:56744195 G>A maps to NM_018261.3 K396K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr4:56744195 G>A maps to NM_018261.3 K396K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr4:77039259 G>A maps to ENST00000458189 Q419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr4:77039259 G>A maps to ENST00000458189 Q419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr4:128637584 C>T maps to NM_015693.3 T941T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr4:128637584 C>T maps to NM_015693.3 T941T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr4:190878614 A>T maps to NM_004477.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr4:190878614 A>T maps to NM_004477.2 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:6609986 T>A maps to NM_017755.5 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:6609986 T>A maps to NM_017755.5 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:7897180 A>G maps to NM_024010.2 K618K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:7897180 A>G maps to NM_024010.2 K618K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:31323141 C>A maps to NM_004932.2 P700P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:31323141 C>A maps to NM_004932.2 P700P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:33461069 G>A maps to ENST00000455217 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:33461069 G>A maps to ENST00000455217 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:35654801 C>T maps to NM_024867.3 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:35654801 C>T maps to NM_024867.3 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:36184010 T>G maps to ENST00000308927 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:36184010 T>G maps to ENST00000308927 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:43382138 G>T maps to NM_148672.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:43382138 G>T maps to NM_148672.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:92923836 G>C maps to NM_005654.4 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:92923836 G>C maps to NM_005654.4 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:137593401 G>T maps to NM_001496.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:137593401 G>T maps to NM_001496.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:140188562 G>A maps to NM_018907.2 V597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:140188562 G>A maps to NM_018907.2 V597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:140209619 G>T maps to NM_018909.2 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:140209619 G>T maps to NM_018909.2 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:140257258 G>T maps to NM_018903.2 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:140257258 G>T maps to NM_018903.2 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:140712445 T>A maps to NM_018912.2 L732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:140712445 T>A maps to NM_018912.2 L732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:140720610 G>T maps to NM_018915.2 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:140720610 G>T maps to NM_018915.2 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:153077674 A>T maps to NM_001114183.1 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:153077674 A>T maps to NM_001114183.1 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:159821206 C>A maps to NM_022090.3 E431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:159821206 C>A maps to NM_022090.3 E431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:160029628 G>A maps to NM_025153.2 Y1106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:160029628 G>A maps to NM_025153.2 Y1106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:160033897 C>A maps to NM_025153.2 E1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:160033897 C>A maps to NM_025153.2 E1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:176489128 C>T maps to ENST00000503039 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:176489128 C>T maps to ENST00000503039 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:178770806 G>A maps to NM_014244.4 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr5:178770806 G>A maps to NM_014244.4 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr6:15468902 G>T maps to NM_004973.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr6:15468902 G>T maps to NM_004973.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr6:33146750 C>A did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr6:33146750 C>A did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr6:41653830 G>T maps to ENST00000343317 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr6:41653830 G>T maps to ENST00000343317 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr6:132722445 G>T maps to NM_015529.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr6:132722445 G>T maps to NM_015529.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr6:133073774 A>G maps to NM_004665.2 Y217Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr6:133073774 A>G maps to NM_004665.2 Y217Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr6:135239567 G>T maps to NM_022568.3 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr6:135239567 G>T maps to NM_022568.3 I483I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr6:166581040 C>G maps to NM_003181.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr6:166581040 C>G maps to NM_003181.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:23682550 G>T maps to NM_138771.3 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:23682550 G>T maps to NM_138771.3 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:28318963 C>A did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:28318963 C>A did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:34009963 G>A maps to NM_133468.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:34009963 G>A maps to NM_133468.3 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:44609414 G>A maps to NM_019082.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:44609414 G>A maps to NM_019082.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:57194380 C>T maps to NM_033273.1 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:57194380 C>T maps to NM_033273.1 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:63680232 C>A maps to NM_001159524.1 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:63680232 C>A maps to NM_001159524.1 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:72718296 C>A maps to NM_148956.2 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:72718296 C>A maps to NM_148956.2 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:82584628 T>A maps to NM_033026.5 V1880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:82584628 T>A maps to NM_033026.5 V1880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:113518192 G>T maps to NM_002711.3 S985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:113518192 G>T maps to NM_002711.3 S985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:122338456 G>A maps to NM_139175.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:122338456 G>A maps to NM_139175.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:140125808 C>T maps to ENST00000275874 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:140125808 C>T maps to ENST00000275874 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:141478515 G>A maps to NM_016944.1 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:141478515 G>A maps to NM_016944.1 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:143657596 C>T maps to NM_012369.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:143657596 C>T maps to NM_012369.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:150164298 G>A maps to NM_175571.2 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:150164298 G>A maps to NM_175571.2 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:150784094 G>T maps to NM_031946.4 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr7:150784094 G>T maps to NM_031946.4 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:1497719 G>A maps to ENST00000357934 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:1497719 G>A maps to ENST00000357934 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:29037626 C>T maps to NM_015254.3 K238K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:29037626 C>T maps to NM_015254.3 K238K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:56879419 G>T maps to NM_002350.2 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:56879419 G>T maps to NM_002350.2 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:87126073 C>A maps to NM_152565.1 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:87126073 C>A maps to NM_152565.1 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:89128828 G>A maps to NM_005941.4 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:89128828 G>A maps to NM_005941.4 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:90777690 G>A maps to NM_003821.5 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:90777690 G>A maps to NM_003821.5 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:93027016 G>A maps to NM_175634.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:93027016 G>A maps to NM_175634.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:146017245 C>A maps to NM_000973.3 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr8:146017245 C>A maps to NM_000973.3 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr9:32633171 G>A maps to NM_153809.2 G802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr9:32633171 G>A maps to NM_153809.2 G802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:5821197 G>T maps to ENST00000381093 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:5821197 G>T maps to ENST00000381093 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:12632925 G>A maps to ENST00000429478 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:12632925 G>A maps to ENST00000429478 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:30260833 C>A maps to NM_002367.3 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:30260833 C>A maps to NM_002367.3 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:30327198 C>T maps to NM_000475.4 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:30327198 C>T maps to NM_000475.4 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:47272965 T>G maps to NM_003446.3 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:47272965 T>G maps to NM_003446.3 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:48370282 G>A maps to NM_203475.1 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:48370282 G>A maps to NM_203475.1 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:48762558 G>A maps to ENST00000452555 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:48762558 G>A maps to ENST00000452555 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:49099870 C>T maps to NM_014008.3 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:49099870 C>T maps to NM_014008.3 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:49958927 C>A maps to NM_003886.2 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:49958927 C>A maps to NM_003886.2 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:53276217 G>A maps to NM_001111125.1 D894D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:53276217 G>A maps to NM_001111125.1 D894D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:86919889 G>A maps to NM_057162.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:86919889 G>A maps to NM_057162.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:135429617 C>A maps to NM_153834.3 T1251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:135429617 C>A maps to NM_153834.3 T1251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:135431249 T>G maps to NM_153834.3 T1795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:135431249 T>G maps to NM_153834.3 T1795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:154493402 G>C maps to NM_171998.2 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chrX:154493402 G>C maps to NM_171998.2 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:22157583 C>G did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:22157583 C>G did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:34092181 C>T did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:34092181 C>T did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:55059687 C>T maps to NM_015547.3 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:55059687 C>T maps to NM_015547.3 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:117656089 C>G maps to NM_025188.3 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:117656089 C>G maps to NM_025188.3 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:155240768 C>G did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:155240768 C>G did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:156621473 G>A maps to NM_021948.3 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:156621473 G>A maps to NM_021948.3 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:156849867 C>T maps to NM_002529.3 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:156849867 C>T maps to NM_002529.3 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:181058478 G>C maps to NM_016545.4 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr1:181058478 G>C maps to NM_016545.4 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr10:5799598 G>A maps to NM_017782.4 V2283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr10:5799598 G>A maps to NM_017782.4 V2283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr10:34420468 C>G maps to NM_019619.3 L1157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr10:34420468 C>G maps to NM_019619.3 L1157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr10:118969464 T>C maps to NM_181840.1 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr10:118969464 T>C maps to NM_181840.1 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr10:119768712 A>T maps to ENST00000369199 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr10:119768712 A>T maps to ENST00000369199 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:4945473 G>T maps to NM_001005237.1 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:4945473 G>T maps to NM_001005237.1 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:5653888 G>T maps to NM_001003819.3 E464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:5653888 G>T maps to NM_001003819.3 E464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:6913476 C>A maps to NM_003700.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:6913476 C>A maps to NM_003700.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:18741304 C>A maps to NM_173588.3 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:18741304 C>A maps to NM_173588.3 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:33768855 T>C maps to NM_012175.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:33768855 T>C maps to NM_012175.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:57118258 C>T maps to NM_002559.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:57118258 C>T maps to NM_002559.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:59271773 C>T maps to NM_001004706.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:59271773 C>T maps to NM_001004706.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:60215207 T>C maps to NM_023945.2 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:60215207 T>C maps to NM_023945.2 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:77301378 C>A maps to NM_173039.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:77301378 C>A maps to NM_173039.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:124252329 G>A maps to NM_001005468.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:124252329 G>A maps to NM_001005468.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:125484216 A>G did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:125484216 A>G did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:130318900 C>T maps to NM_139055.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr11:130318900 C>T maps to NM_139055.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr12:8691818 C>A maps to NM_014358.2 G72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr12:8691818 C>A maps to NM_014358.2 G72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr12:100955660 A>T did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr12:100955660 A>T did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr12:108589737 C>T maps to ENST00000261400 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr12:108589737 C>T maps to ENST00000261400 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr12:124008156 C>T maps to NM_178314.3 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr12:124008156 C>T maps to NM_178314.3 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:20849804 G>A maps to NM_007110.4 L1489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:20849804 G>A maps to NM_007110.4 L1489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:22133981 C>G maps to NM_001001912.1 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:22133981 C>G maps to NM_001001912.1 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:33684489 T>A maps to NM_001164749.1 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:33684489 T>A maps to NM_001164749.1 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:37754563 G>T maps to NM_001195296.1 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:37754563 G>T maps to NM_001195296.1 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:38679679 C>A maps to NM_001049.2 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:38679679 C>A maps to NM_001049.2 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:74761851 T>A maps to NM_005050.3 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:74761851 T>A maps to NM_005050.3 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:89305908 A>G maps to NM_144596.2 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:89305908 A>G maps to NM_144596.2 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:91780145 G>A maps to NM_001080414.2 Q672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:91780145 G>A maps to NM_001080414.2 Q672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:102028009 C>G maps to NM_001362.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr14:102028009 C>G maps to NM_001362.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr16:1996718 G>C maps to NM_005061.2 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr16:1996718 G>C maps to NM_005061.2 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr16:30518131 G>C maps to NM_002209.2 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr16:30518131 G>C maps to NM_002209.2 L821L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CR-7371-01A-11D-2012-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CR-7371-01A-11D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr16:71406096 C>T maps to NM_001740.4 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr16:71406096 C>T maps to NM_001740.4 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr16:84808829 A>T maps to NM_005153.2 A736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr16:84808829 A>T maps to NM_005153.2 A736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr17:26107911 C>T maps to NM_000625.4 W295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr17:26107911 C>T maps to NM_000625.4 W295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr17:46135824 G>T maps to ENST00000362042 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr17:46135824 G>T maps to ENST00000362042 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr17:56620419 G>C maps to NM_001038704.1 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr17:56620419 G>C maps to NM_001038704.1 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr17:62122728 G>A maps to NM_001433.3 P881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr17:62122728 G>A maps to NM_001433.3 P881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr17:73498199 C>A maps to NM_020753.3 T985T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr17:73498199 C>A maps to NM_020753.3 T985T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr18:33828963 G>T did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr18:33828963 G>T did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr19:1043351 G>C maps to NM_019112.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr19:1043351 G>C maps to NM_019112.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr19:9056572 G>A maps to NM_024690.2 T10291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr19:9056572 G>A maps to NM_024690.2 T10291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr19:12297489 G>A maps to NM_003437.3 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr19:12297489 G>A maps to NM_003437.3 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:25050955 C>T maps to NM_004036.3 E749E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:25050955 C>T maps to NM_004036.3 E749E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:37217853 G>C maps to NM_019024.1 V1878V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:37217853 G>C maps to NM_019024.1 V1878V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:96689185 G>A maps to NM_207328.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:96689185 G>A maps to NM_207328.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:143712376 A>G did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:143712376 A>G did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:179259093 G>A maps to ENST00000392505 E901E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:179259093 G>A maps to ENST00000392505 E901E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:179579977 G>A maps to NM_133378.4 F7401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:179579977 G>A maps to NM_133378.4 F7401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:183731214 G>A maps to NM_001463.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:183731214 G>A maps to NM_001463.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:202005137 C>T maps to NM_001127183.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:202005137 C>T maps to NM_001127183.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:242662622 A>T did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr2:242662622 A>T did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr20:31620829 G>A maps to NM_174897.2 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr20:31620829 G>A maps to NM_174897.2 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr21:46596173 G>A maps to NM_015833.3 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr21:46596173 G>A maps to NM_015833.3 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr22:21799709 C>T maps to NM_015094.2 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr22:21799709 C>T maps to NM_015094.2 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr22:30412530 G>A maps to NM_021090.3 Q506Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr22:30412530 G>A maps to NM_021090.3 Q506Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr22:30977574 C>T maps to NM_014303.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr22:30977574 C>T maps to NM_014303.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr22:44585009 C>T maps to NM_001137606.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr22:44585009 C>T maps to NM_001137606.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr22:47033857 G>T did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr22:47033857 G>T did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr22:47095334 G>T maps to NM_022766.5 S273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr22:47095334 G>T maps to NM_022766.5 S273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:47712146 C>A did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:47712146 C>A did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:74350692 C>A maps to NM_020872.1 E651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:74350692 C>A maps to NM_020872.1 E651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:87325509 G>A maps to NM_001122757.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:87325509 G>A maps to NM_001122757.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:123019031 G>A maps to NM_183357.2 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:123019031 G>A maps to NM_183357.2 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:130463594 G>A maps to NM_014602.2 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:130463594 G>A maps to NM_014602.2 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:141622515 C>G maps to NM_001679.2 S55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:141622515 C>G maps to NM_001679.2 S55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:179051457 C>T maps to NM_016331.1 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:179051457 C>T maps to NM_016331.1 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:194169312 C>T maps to NM_024524.3 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:194169312 C>T maps to NM_024524.3 V341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:195451994 C>G maps to ENST00000447234 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr3:195451994 C>G maps to ENST00000447234 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:42602536 T>A did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:42602536 T>A did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:57221513 G>A maps to NM_181806.2 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:57221513 G>A maps to NM_181806.2 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:89668808 C>A maps to NM_014883.2 A785A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:89668808 C>A maps to NM_014883.2 A785A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:104035709 C>T did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:104035709 C>T did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:114376955 C>T maps to ENST00000515496 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:114376955 C>T maps to ENST00000515496 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:134084408 G>T maps to NM_032961.1 T1025T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:134084408 G>T maps to NM_032961.1 T1025T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:139980634 C>T maps to ENST00000379550 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:139980634 C>T maps to ENST00000379550 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:153247310 C>T maps to NM_033632.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:153247310 C>T maps to NM_033632.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:176573009 A>G maps to NM_005277.3 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr4:176573009 A>G maps to NM_005277.3 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr5:7717277 C>A maps to NM_020546.2 S544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr5:7717277 C>A maps to NM_020546.2 S544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr5:11236805 G>T maps to NM_001332.2 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr5:11236805 G>T maps to NM_001332.2 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr5:63256364 C>A maps to NM_000524.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr5:63256364 C>A maps to NM_000524.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr5:63256922 C>A maps to NM_000524.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr5:63256922 C>A maps to NM_000524.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr5:140562679 C>T maps to NM_020957.1 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr5:140562679 C>T maps to NM_020957.1 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr5:180057696 G>A maps to NM_182925.4 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr5:180057696 G>A maps to NM_182925.4 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr6:70040461 C>T maps to NM_001704.2 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr6:70040461 C>T maps to NM_001704.2 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr6:96651726 T>C maps to NM_006581.3 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr6:96651726 T>C maps to NM_006581.3 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr6:133802715 G>T maps to ENST00000452339 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr6:133802715 G>T maps to ENST00000452339 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr7:47913504 G>A maps to NM_138295.3 G1296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr7:47913504 G>A maps to NM_138295.3 G1296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr7:55221792 G>A maps to NM_005228.3 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr7:55221792 G>A maps to NM_005228.3 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr7:99124009 A>G maps to NM_014569.3 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr7:99124009 A>G maps to NM_014569.3 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr7:123516941 C>T maps to NM_012269.2 N393N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr7:123516941 C>T maps to NM_012269.2 N393N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr7:141952172 C>T maps to NM_001001317.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr7:141952172 C>T maps to NM_001001317.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:1876768 G>C maps to ENST00000398564 V983V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:1876768 G>C maps to ENST00000398564 V983V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:28196681 C>T maps to NM_006228.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:28196681 C>T maps to NM_006228.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:41798737 G>C maps to NM_006766.3 L887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:41798737 G>C maps to NM_006766.3 L887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:100831005 G>A maps to NM_017890.3 E2862E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:100831005 G>A maps to NM_017890.3 E2862E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:139155261 G>T maps to NM_015912.3 R1211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:139155261 G>T maps to NM_015912.3 R1211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:139165259 C>T maps to NM_015912.3 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:139165259 C>T maps to NM_015912.3 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:139614356 C>A did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:139614356 C>A did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:143425408 G>T maps to ENST00000445818 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr8:143425408 G>T maps to ENST00000445818 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr9:27950477 G>A maps to NM_152570.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr9:27950477 G>A maps to NM_152570.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr9:72435948 T>A did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr9:72435948 T>A did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr9:79320153 C>A maps to NM_015225.2 E2346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr9:79320153 C>A maps to NM_015225.2 E2346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr9:111903625 G>A maps to NM_014334.2 Q287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr9:111903625 G>A maps to NM_014334.2 Q287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr9:114676935 C>T maps to NM_003358.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr9:114676935 C>T maps to NM_003358.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr9:133993217 C>G maps to NM_001185095.1 S119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr9:133993217 C>G maps to NM_001185095.1 S119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr9:134308155 A>T maps to NM_013318.3 K90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chr9:134308155 A>T maps to NM_013318.3 K90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chrX:31496267 G>C maps to ENST00000357033 G2964G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chrX:31496267 G>C maps to ENST00000357033 G2964G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chrX:70146773 G>A maps to NM_032803.5 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chrX:70146773 G>A maps to NM_032803.5 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr1:198723446 G>T maps to ENST00000271610 E1187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr1:198723446 G>T maps to ENST00000271610 E1187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr1:223177008 C>A maps to NM_032890.2 S757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr1:223177008 C>A maps to NM_032890.2 S757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr10:115962044 G>A maps to NM_198795.1 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr10:115962044 G>A maps to NM_198795.1 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr11:56258615 A>G maps to NM_001005282.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr11:56258615 A>G maps to NM_001005282.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr12:11461742 T>C maps to NM_002723.3 Q58Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr12:11461742 T>C maps to NM_002723.3 Q58Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr12:133215739 G>A maps to ENST00000455752 L1844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr12:133215739 G>A maps to ENST00000455752 L1844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr15:43705365 G>A maps to NM_001141980.1 S1752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr15:43705365 G>A maps to NM_001141980.1 S1752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr15:54542505 G>A maps to ENST00000260323 T1104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr15:54542505 G>A maps to ENST00000260323 T1104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr15:89871965 G>A maps to NM_002693.2 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr15:89871965 G>A maps to NM_002693.2 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr18:32443989 A>G maps to NM_001390.4 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr18:32443989 A>G maps to NM_001390.4 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr19:1784855 G>A maps to NM_138813.2 R1208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr19:1784855 G>A maps to NM_138813.2 R1208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr19:42793502 G>A maps to NM_015125.3 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr19:42793502 G>A maps to NM_015125.3 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr19:50549980 C>T maps to NM_015428.1 Q761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr19:50549980 C>T maps to NM_015428.1 Q761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr3:46728523 G>A maps to NM_147129.3 H161H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr3:46728523 G>A maps to NM_147129.3 H161H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr4:114469878 A>G maps to ENST00000515496 C116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr4:114469878 A>G maps to ENST00000515496 C116C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr6:114379097 C>A maps to NM_153612.3 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr6:114379097 C>A maps to NM_153612.3 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr7:121691547 A>T maps to NM_002851.2 K2051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr7:121691547 A>T maps to NM_002851.2 K2051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr8:110477208 G>T maps to ENST00000426474 L2716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr8:110477208 G>T maps to ENST00000426474 L2716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr8:140630971 C>T maps to NM_016601.2 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7372-01A-11D-2012-08 chr8:140630971 C>T maps to NM_016601.2 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr1:14925657 C>T maps to NM_201628.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr1:14925657 C>T maps to NM_201628.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr1:94342344 G>A maps to NM_014597.4 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr1:94342344 G>A maps to NM_014597.4 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr1:112309064 C>T maps to NM_007204.4 Y673Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr1:112309064 C>T maps to NM_007204.4 Y673Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr1:152883938 C>T maps to NM_005547.2 Q556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr1:152883938 C>T maps to NM_005547.2 Q556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr1:153533986 C>T maps to ENST00000368707 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr1:153533986 C>T maps to ENST00000368707 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr1:221913035 G>A maps to NM_007207.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr1:221913035 G>A maps to NM_007207.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr10:30900883 T>A maps to NM_183058.2 *195Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr10:30900883 T>A maps to NM_183058.2 *195Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr10:106113660 T>A maps to NM_001008723.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr10:106113660 T>A maps to NM_001008723.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr11:6891449 C>T maps to NM_001004460.1 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr11:6891449 C>T maps to NM_001004460.1 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr11:59857260 G>A maps to NM_000139.4 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr11:59857260 G>A maps to NM_000139.4 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr11:71822258 G>T maps to NM_014042.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr11:71822258 G>T maps to NM_014042.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr11:94134044 G>C maps to NM_016540.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr11:94134044 G>C maps to NM_016540.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr11:124750347 C>T maps to NM_022370.3 F1331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr11:124750347 C>T maps to NM_022370.3 F1331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr11:133792106 G>C maps to NM_014987.1 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr11:133792106 G>C maps to NM_014987.1 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr12:4409144 C>T maps to NM_001759.3 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr12:4409144 C>T maps to NM_001759.3 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr12:13722779 C>A maps to NM_000834.3 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr12:13722779 C>A maps to NM_000834.3 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr12:114804165 G>C maps to NM_000192.3 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr12:114804165 G>C maps to NM_000192.3 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr13:77715010 G>C maps to NM_015057.4 V2457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr13:77715010 G>C maps to NM_015057.4 V2457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr14:20345328 G>C maps to NM_001005501.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr14:20345328 G>C maps to NM_001005501.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr15:84286873 C>G maps to ENST00000434347 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr15:84286873 C>G maps to ENST00000434347 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr15:85669604 G>A maps to NM_002605.2 Q751Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr15:85669604 G>A maps to NM_002605.2 Q751Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr15:90143869 C>T maps to NM_152259.3 R703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr15:90143869 C>T maps to NM_152259.3 R703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr16:28883682 T>G maps to NM_001145795.1 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr16:28883682 T>G maps to NM_001145795.1 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr16:28906159 G>A maps to NM_173201.3 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr16:28906159 G>A maps to NM_173201.3 E435E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CR-7373-01A-11D-2012-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CR-7373-01A-11D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr16:86580198 T>C maps to NM_001159377.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr16:86580198 T>C maps to NM_001159377.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr17:4847868 C>T maps to NM_015528.1 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr17:4847868 C>T maps to NM_015528.1 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr17:18144787 C>T maps to NM_004140.3 S842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr17:18144787 C>T maps to NM_004140.3 S842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr17:44248385 G>C maps to NM_015443.3 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr17:44248385 G>C maps to NM_015443.3 S375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr17:54940146 G>T maps to NM_003647.2 E567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr17:54940146 G>T maps to NM_003647.2 E567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr17:73751884 G>A maps to NM_001005619.1 E1537E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr17:73751884 G>A maps to NM_001005619.1 E1537E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr19:15290214 G>A maps to NM_000435.2 L1140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr19:15290214 G>A maps to NM_000435.2 L1140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr19:50098965 G>T maps to NM_020719.1 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr19:50098965 G>T maps to NM_020719.1 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr19:50958902 T>C did not map to a codon.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr19:50958902 T>C did not map to a codon.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr2:24261334 G>A maps to NM_025203.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr2:24261334 G>A maps to NM_025203.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr2:24261746 G>C maps to NM_025203.2 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr2:24261746 G>C maps to NM_025203.2 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr2:98408978 C>T maps to NM_015348.1 A1338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr2:98408978 C>T maps to NM_015348.1 A1338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr20:23966390 G>A maps to NM_178311.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr20:23966390 G>A maps to NM_178311.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr20:35695459 A>G maps to NM_002895.2 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr20:35695459 A>G maps to NM_002895.2 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr3:40570901 G>A maps to NM_001098414.1 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr3:40570901 G>A maps to NM_001098414.1 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr3:168834350 C>A maps to NM_004991.3 G437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr3:168834350 C>A maps to NM_004991.3 G437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr5:149754238 C>A maps to ENST00000451292 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr5:149754238 C>A maps to ENST00000451292 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr6:2675331 G>C maps to NM_001012418.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr6:2675331 G>C maps to NM_001012418.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr6:29910348 C>T maps to ENST00000376806 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr6:29910348 C>T maps to ENST00000376806 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr6:40359912 C>T maps to NM_020737.1 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr6:40359912 C>T maps to NM_020737.1 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr6:41318600 G>A maps to NM_004828.3 *277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr6:41318600 G>A maps to NM_004828.3 *277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr6:119501046 G>A maps to NM_005907.2 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr6:119501046 G>A maps to NM_005907.2 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr6:126203621 G>A maps to NM_181782.4 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr6:126203621 G>A maps to NM_181782.4 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr7:14378223 G>A maps to NM_004080.2 R681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr7:14378223 G>A maps to NM_004080.2 R681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr8:144557589 G>T maps to NM_015117.2 G627G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr8:144557589 G>T maps to NM_015117.2 G627G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr9:32635388 C>T maps to NM_153809.2 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr9:32635388 C>T maps to NM_153809.2 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr9:33917125 C>G maps to NM_017811.3 S203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr9:33917125 C>G maps to NM_017811.3 S203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr9:134321938 C>T maps to NM_013318.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr9:134321938 C>T maps to NM_013318.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr9:139617955 C>T maps to NM_152421.3 Y342Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chr9:139617955 C>T maps to NM_152421.3 Y342Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chrX:48123287 C>T maps to NM_005635.2 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7373-01A-11D-2012-08 chrX:48123287 C>T maps to NM_005635.2 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:10713621 G>C maps to NM_001079843.1 S831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:10713621 G>C maps to NM_001079843.1 S831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:31423054 G>A maps to ENST00000373741 V961V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:31423054 G>A maps to ENST00000373741 V961V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:48708176 G>T maps to NM_001135181.1 E601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:48708176 G>T maps to NM_001135181.1 E601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:52854209 C>T maps to NM_004153.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:52854209 C>T maps to NM_004153.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:78279428 G>A maps to NM_198549.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:78279428 G>A maps to NM_198549.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:109538249 G>C maps to NM_001142550.1 S556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:109538249 G>C maps to NM_001142550.1 S556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:149783711 G>T maps to ENST00000427880 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:149783711 G>T maps to ENST00000427880 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:152275981 G>A maps to NM_002016.1 Q3794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:152275981 G>A maps to NM_002016.1 Q3794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:190067942 C>T maps to NM_199051.1 Q502Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:190067942 C>T maps to NM_199051.1 Q502Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:216850475 G>C maps to NM_001438.2 Y138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:216850475 G>C maps to NM_001438.2 Y138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:236724550 A>G maps to NM_018072.5 P1540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:236724550 A>G maps to NM_018072.5 P1540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:240256602 C>A maps to ENST00000406993 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:240256602 C>A maps to ENST00000406993 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:247655014 G>T maps to NM_001004698.2 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr1:247655014 G>T maps to NM_001004698.2 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr10:8100436 G>A maps to NM_001002295.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr10:8100436 G>A maps to NM_001002295.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr10:15120600 C>A maps to NM_001039844.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr10:15120600 C>A maps to NM_001039844.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr10:24884717 G>A maps to NM_020824.3 R1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr10:24884717 G>A maps to NM_020824.3 R1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr10:70406352 G>A maps to NM_030625.2 T1289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr10:70406352 G>A maps to NM_030625.2 T1289T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr10:75139820 G>A maps to NM_004034.2 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr10:75139820 G>A maps to NM_004034.2 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:5142451 C>A maps to NM_001005222.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:5142451 C>A maps to NM_001005222.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:17409545 C>T maps to NM_000525.3 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:17409545 C>T maps to NM_000525.3 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:26681843 C>T maps to NM_031418.2 Y933Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:26681843 C>T maps to NM_031418.2 Y933Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:26742937 G>A maps to NM_178498.3 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:26742937 G>A maps to NM_178498.3 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:35222734 G>A maps to NM_000610.3 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:35222734 G>A maps to NM_000610.3 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:55872802 G>T maps to NM_001005200.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:55872802 G>T maps to NM_001005200.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:65651445 C>T maps to NM_198897.1 *365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:65651445 C>T maps to NM_198897.1 *365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:67378580 C>T maps to NM_007103.3 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:67378580 C>T maps to NM_007103.3 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:76063226 C>A maps to NM_004705.2 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:76063226 C>A maps to NM_004705.2 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:121476227 C>G maps to NM_003105.5 L1632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr11:121476227 C>G maps to NM_003105.5 L1632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr12:14976372 C>T maps to NM_175874.3 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr12:14976372 C>T maps to NM_175874.3 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr12:72278769 G>T maps to NM_022771.4 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr12:72278769 G>T maps to NM_022771.4 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr12:107109318 C>T maps to ENST00000357881 Q388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr12:107109318 C>T maps to ENST00000357881 Q388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr12:112711556 G>C maps to NM_001109662.2 S433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr12:112711556 G>C maps to NM_001109662.2 S433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr12:122281717 T>C maps to NM_002150.2 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr12:122281717 T>C maps to NM_002150.2 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr12:123651317 G>A maps to NM_022782.2 D673D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr12:123651317 G>A maps to NM_022782.2 D673D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr13:33016825 C>T maps to NM_033111.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr13:33016825 C>T maps to NM_033111.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr13:48955579 G>A did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr13:48955579 G>A did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr14:62550912 G>A did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr14:62550912 G>A did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr14:64954377 G>A maps to NM_006977.2 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr14:64954377 G>A maps to NM_006977.2 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr14:86088199 C>T maps to NM_013231.4 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr14:86088199 C>T maps to NM_013231.4 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr14:92625449 G>T maps to NM_017437.1 E649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr14:92625449 G>T maps to NM_017437.1 E649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr15:22332525 C>A did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr15:22332525 C>A did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr15:48577393 C>T maps to NM_000338.2 G859G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr15:48577393 C>T maps to NM_000338.2 G859G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr15:79292108 G>T maps to NM_002891.4 R924R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr15:79292108 G>T maps to NM_002891.4 R924R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr15:89015920 G>A maps to NM_022839.3 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr15:89015920 G>A maps to NM_022839.3 E82E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr15:89862532 G>A maps to NM_002693.2 L1010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr15:89862532 G>A maps to NM_002693.2 L1010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:20439172 C>T maps to NM_017888.2 Q329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:20439172 C>T maps to NM_017888.2 Q329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:20476885 G>A maps to NM_001010845.2 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:20476885 G>A maps to NM_001010845.2 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:20570721 C>T maps to NM_182617.3 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:20570721 C>T maps to NM_182617.3 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:30495264 C>T maps to NM_002209.2 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:30495264 C>T maps to NM_002209.2 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:30779632 G>A maps to NM_014771.2 E587E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:30779632 G>A maps to NM_014771.2 E587E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:66881110 T>C maps to NM_005182.2 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:66881110 T>C maps to NM_005182.2 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:67913614 G>T maps to NM_014329.3 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:67913614 G>T maps to NM_014329.3 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:68729191 G>A maps to NM_001793.4 K679K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:68729191 G>A maps to NM_001793.4 K679K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:71570717 G>T maps to NM_001166395.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr16:71570717 G>T maps to NM_001166395.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr17:2323538 C>A maps to NM_024086.3 G472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr17:2323538 C>A maps to NM_024086.3 G472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr17:10353771 G>T maps to NM_017533.2 A1393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr17:10353771 G>T maps to NM_017533.2 A1393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr17:18070959 C>T maps to ENST00000205890 S3335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr17:18070959 C>T maps to ENST00000205890 S3335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr17:38906821 C>A maps to NM_181534.3 E329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr17:38906821 C>A maps to NM_181534.3 E329*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CR-7374-01A-11D-2012-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CR-7374-01A-11D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr18:29052737 C>T maps to NM_001944.2 F696F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr18:29052737 C>T maps to NM_001944.2 F696F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:2109957 C>G did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:2109957 C>G did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:6924813 G>T maps to ENST00000381407 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:6924813 G>T maps to ENST00000381407 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:7697682 G>A maps to NM_174895.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:7697682 G>A maps to NM_174895.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:7965434 A>T maps to NM_025061.3 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:7965434 A>T maps to NM_025061.3 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:9069583 A>T maps to NM_024690.2 A5954A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:9069583 A>T maps to NM_024690.2 A5954A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:14090330 T>A maps to NM_002918.4 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:14090330 T>A maps to NM_002918.4 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:35800951 G>T maps to NM_002361.3 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:35800951 G>T maps to NM_002361.3 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:36362533 C>T maps to NM_001024807.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:36362533 C>T maps to NM_001024807.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:44376784 T>C maps to ENST00000324394 E525E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:44376784 T>C maps to ENST00000324394 E525E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:54318202 G>C maps to ENST00000391773 S110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:54318202 G>C maps to ENST00000391773 S110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:55106847 C>A maps to NM_006863.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr19:55106847 C>A maps to NM_006863.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:88424027 G>A maps to NM_001443.1 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:88424027 G>A maps to NM_001443.1 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:116257181 T>A did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:116257181 T>A did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:167056096 A>G maps to ENST00000303354 F1685F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:167056096 A>G maps to ENST00000303354 F1685F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:168107804 G>A maps to NM_152381.5 V3301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:168107804 G>A maps to NM_152381.5 V3301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:180383317 G>T maps to NM_152520.4 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:180383317 G>T maps to NM_152520.4 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:209180090 C>T maps to NM_015040.3 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:209180090 C>T maps to NM_015040.3 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:211018890 G>C maps to NM_152519.2 S139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:211018890 G>C maps to NM_152519.2 S139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:216269262 G>A maps to NM_212482.1 T1034T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr2:216269262 G>A maps to NM_212482.1 T1034T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr20:4865410 G>A maps to NM_203327.1 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr20:4865410 G>A maps to NM_203327.1 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr20:20350276 C>T maps to NM_002196.2 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr20:20350276 C>T maps to NM_002196.2 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr20:31652344 G>T maps to NM_182658.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr20:31652344 G>T maps to NM_182658.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr20:62321523 C>T maps to ENST00000482936 I742I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr20:62321523 C>T maps to ENST00000482936 I742I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr21:34003712 G>A maps to NM_003895.3 I1477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr21:34003712 G>A maps to NM_003895.3 I1477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr22:47033813 C>T maps to NM_015124.2 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr22:47033813 C>T maps to NM_015124.2 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr22:50860745 C>T maps to ENST00000216061 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr22:50860745 C>T maps to ENST00000216061 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr3:43596800 G>C maps to NM_018075.3 S546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr3:43596800 G>C maps to NM_018075.3 S546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr3:46482937 C>A maps to NM_002343.3 V564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr3:46482937 C>A maps to NM_002343.3 V564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr3:47049353 C>G maps to NM_015175.1 S2519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr3:47049353 C>G maps to NM_015175.1 S2519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr3:112647681 C>A maps to NM_138806.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr3:112647681 C>A maps to NM_138806.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr3:150690258 C>T maps to NM_001195794.1 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr3:150690258 C>T maps to NM_001195794.1 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr3:160120572 C>A maps to NM_005496.3 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr3:160120572 C>A maps to NM_005496.3 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr3:169492265 C>G maps to NM_018657.4 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr3:169492265 C>G maps to NM_018657.4 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr4:79285131 C>G maps to NM_025074.6 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr4:79285131 C>G maps to NM_025074.6 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr4:109822295 C>T maps to ENST00000333642 Q271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr4:109822295 C>T maps to ENST00000333642 Q271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr4:123155981 A>G maps to NM_015312.3 K1126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr4:123155981 A>G maps to NM_015312.3 K1126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr4:176573000 C>T maps to NM_005277.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr4:176573000 C>T maps to NM_005277.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr4:187521276 C>A maps to ENST00000260147 G3963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr4:187521276 C>A maps to ENST00000260147 G3963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:11023076 G>A maps to NM_001332.2 R935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:11023076 G>A maps to NM_001332.2 R935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:35039553 C>T maps to NM_031900.3 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:35039553 C>T maps to NM_031900.3 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:80640769 G>A maps to NM_130767.2 Y288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:80640769 G>A maps to NM_130767.2 Y288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:90106676 T>A maps to NM_032119.3 A5200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:90106676 T>A maps to NM_032119.3 A5200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:113831599 C>T maps to NM_021614.2 N487N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:113831599 C>T maps to NM_021614.2 N487N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:140581329 C>G maps to NM_018931.2 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:140581329 C>G maps to NM_018931.2 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:140719456 C>T maps to NM_018915.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:140719456 C>T maps to NM_018915.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:140795001 C>T maps to NM_018913.2 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:140795001 C>T maps to NM_018913.2 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:145439600 C>T maps to NM_152550.3 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr5:145439600 C>T maps to NM_152550.3 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:26197325 C>T maps to NM_003530.3 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:26197325 C>T maps to NM_003530.3 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:28541502 A>C maps to NM_052923.1 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:28541502 A>C maps to NM_052923.1 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:33287563 G>C maps to NM_001350.4 G511G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:33287563 G>C maps to NM_001350.4 G511G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:35378950 C>G maps to NM_006238.4 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:35378950 C>G maps to NM_006238.4 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:38759380 C>T maps to ENST00000327475 A932A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:38759380 C>T maps to ENST00000327475 A932A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:71185188 T>C maps to NM_001162529.1 N78N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:71185188 T>C maps to NM_001162529.1 N78N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:136990453 G>A maps to NM_005923.3 Q445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:136990453 G>A maps to NM_005923.3 Q445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:147684645 G>A maps to NM_001127715.1 Q907Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr6:147684645 G>A maps to NM_001127715.1 Q907Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr7:5353144 C>T maps to NM_001080495.2 E2459E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr7:5353144 C>T maps to NM_001080495.2 E2459E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr7:44091507 C>T maps to NM_001122956.1 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr7:44091507 C>T maps to NM_001122956.1 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr7:56147374 C>T maps to NM_001130069.1 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr7:56147374 C>T maps to NM_001130069.1 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr7:87056097 G>A maps to NM_018849.2 Q678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr7:87056097 G>A maps to NM_018849.2 Q678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr8:35608236 G>T maps to ENST00000416672 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr8:35608236 G>T maps to ENST00000416672 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr8:41792080 T>C maps to NM_006766.3 L1219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr8:41792080 T>C maps to NM_006766.3 L1219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr8:113668539 C>G maps to NM_198123.1 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr8:113668539 C>G maps to NM_198123.1 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr8:144358698 C>T maps to NM_138465.3 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr8:144358698 C>T maps to NM_138465.3 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr8:144463845 G>A maps to ENST00000422773 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr8:144463845 G>A maps to ENST00000422773 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr9:84609740 G>A maps to NM_001001670.2 E1452E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr9:84609740 G>A maps to NM_001001670.2 E1452E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr9:130485520 C>T maps to NM_144965.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr9:130485520 C>T maps to NM_144965.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr9:131768857 G>A maps to NM_015354.1 S1717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr9:131768857 G>A maps to NM_015354.1 S1717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chrX:36162676 G>C did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chrX:36162676 G>C did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chrX:54469924 G>T did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chrX:54469924 G>T did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chrX:144906313 C>T maps to NM_001144010.2 R791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chrX:144906313 C>T maps to NM_001144010.2 R791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr1:12920036 C>T maps to NM_023014.1 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr1:12920036 C>T maps to NM_023014.1 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr1:43812538 G>A maps to NM_005373.2 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr1:43812538 G>A maps to NM_005373.2 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr10:77818490 C>T maps to NM_032024.3 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr10:77818490 C>T maps to NM_032024.3 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr11:1018366 T>A maps to NM_005961.2 S1478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr11:1018366 T>A maps to NM_005961.2 S1478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr11:1501644 G>A maps to NM_001172223.1 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr11:1501644 G>A maps to NM_001172223.1 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr12:9251235 G>A maps to NM_000014.4 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr12:9251235 G>A maps to NM_000014.4 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr12:121867997 G>T did not map to a codon.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr12:121867997 G>T did not map to a codon.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr13:36229803 C>T maps to ENST00000400445 I2739I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr13:36229803 C>T maps to ENST00000400445 I2739I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr17:48273001 G>A maps to NM_000088.3 R361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr17:48273001 G>A maps to NM_000088.3 R361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr19:51532605 A>G maps to NM_019598.2 Y233Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr19:51532605 A>G maps to NM_019598.2 Y233Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr2:1652026 G>C maps to NM_012293.1 V1175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr2:1652026 G>C maps to NM_012293.1 V1175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr2:212587118 T>C maps to NM_005235.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr2:212587118 T>C maps to NM_005235.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr3:11389502 C>T maps to NM_006395.2 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr3:11389502 C>T maps to NM_006395.2 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr3:30713558 C>G maps to NM_001024847.2 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr3:30713558 C>G maps to NM_001024847.2 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr3:58514634 G>C maps to NM_003500.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr3:58514634 G>C maps to NM_003500.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr3:98251011 G>T maps to NM_005290.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr3:98251011 G>T maps to NM_005290.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr5:139747330 C>G maps to ENST00000507527 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr5:139747330 C>G maps to ENST00000507527 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr7:91682105 C>G maps to NM_005751.4 S1812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr7:91682105 C>G maps to NM_005751.4 S1812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr7:100205593 G>A maps to NM_002593.3 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr7:100205593 G>A maps to NM_002593.3 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr8:69005940 T>C maps to NM_024870.2 F784F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr8:69005940 T>C maps to NM_024870.2 F784F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr9:36236907 T>A maps to NM_001128227.2 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7376-01A-11D-2129-08 chr9:36236907 T>A maps to NM_001128227.2 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr1:100572485 G>A maps to NM_194292.1 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr1:100572485 G>A maps to NM_194292.1 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr1:117492009 G>A maps to NM_020440.2 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr1:117492009 G>A maps to NM_020440.2 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr1:182554926 G>A maps to NM_021133.3 Q339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr1:182554926 G>A maps to NM_021133.3 Q339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr1:203276430 G>A maps to NM_006763.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr1:203276430 G>A maps to NM_006763.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr1:208061163 A>T maps to NM_001025109.1 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr1:208061163 A>T maps to NM_001025109.1 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr1:248616313 C>A maps to NM_001004136.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr1:248616313 C>A maps to NM_001004136.1 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr10:6255709 A>G maps to NM_004566.3 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr10:6255709 A>G maps to NM_004566.3 K67K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr11:76919560 C>T maps to NM_000260.3 D1981D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr11:76919560 C>T maps to NM_000260.3 D1981D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr12:21668637 A>G maps to NM_016072.4 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr12:21668637 A>G maps to NM_016072.4 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr12:48543151 T>C maps to NM_024095.3 E288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr12:48543151 T>C maps to NM_024095.3 E288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr12:49521799 C>A maps to NM_006082.2 E433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr12:49521799 C>A maps to NM_006082.2 E433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr12:72091108 A>G maps to NM_018279.3 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr12:72091108 A>G maps to NM_018279.3 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr12:108102725 A>G maps to NM_007062.1 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr12:108102725 A>G maps to NM_007062.1 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr13:46287816 G>A maps to NM_152719.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr13:46287816 G>A maps to NM_152719.1 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr13:73334726 G>T maps to NM_014953.3 I911I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr13:73334726 G>T maps to NM_014953.3 I911I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr13:111299461 C>T maps to NM_024537.2 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr13:111299461 C>T maps to NM_024537.2 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr13:111973248 G>T maps to NM_152324.1 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr13:111973248 G>T maps to NM_152324.1 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr14:20917163 G>A maps to NM_017807.3 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr14:20917163 G>A maps to NM_017807.3 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr14:94089059 C>T maps to ENST00000393153 S1849S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr14:94089059 C>T maps to ENST00000393153 S1849S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr16:20994155 C>T maps to NM_017539.1 S2582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr16:20994155 C>T maps to NM_017539.1 S2582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr17:49825157 G>A maps to NM_001082534.1 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr17:49825157 G>A maps to NM_001082534.1 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr19:13035606 C>T maps to NM_004461.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr19:13035606 C>T maps to NM_004461.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr19:22939798 G>A maps to ENST00000397104 A844A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr19:22939798 G>A maps to ENST00000397104 A844A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr19:34984492 G>T maps to ENST00000270288 E557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr19:34984492 G>T maps to ENST00000270288 E557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr19:36212435 C>T maps to NM_014727.1 N729N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr19:36212435 C>T maps to NM_014727.1 N729N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr2:40397430 G>A maps to NM_021097.2 I676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr2:40397430 G>A maps to NM_021097.2 I676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr2:128029026 T>A maps to NM_000122.1 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr2:128029026 T>A maps to NM_000122.1 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr20:57767312 C>T maps to NM_178457.1 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr20:57767312 C>T maps to NM_178457.1 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr22:50720045 C>T maps to NM_012401.2 P1157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr22:50720045 C>T maps to NM_012401.2 P1157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr3:3887530 G>C maps to NM_020873.5 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr3:3887530 G>C maps to NM_020873.5 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr3:97868270 C>T maps to NM_001005514.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr3:97868270 C>T maps to NM_001005514.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr3:100469362 C>T maps to ENST00000471714 G1770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr3:100469362 C>T maps to ENST00000471714 G1770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr3:108746687 G>A maps to NM_014429.3 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr3:108746687 G>A maps to NM_014429.3 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr3:109047777 C>T maps to NM_018189.3 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr3:109047777 C>T maps to NM_018189.3 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr4:162306901 G>A maps to NM_020116.3 A847A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr4:162306901 G>A maps to NM_020116.3 A847A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr4:185681654 C>T did not map to a codon.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr4:185681654 C>T did not map to a codon.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr5:54565330 C>T maps to NM_019030.2 P1068P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr5:54565330 C>T maps to NM_019030.2 P1068P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr5:145719961 C>T maps to NM_002700.2 N324N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr5:145719961 C>T maps to NM_002700.2 N324N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr6:30140092 G>A maps to NM_033229.2 W455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr6:30140092 G>A maps to NM_033229.2 W455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr6:38649809 T>C maps to NM_006708.2 K148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr6:38649809 T>C maps to NM_006708.2 K148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr6:43322833 T>C maps to NM_014345.2 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr6:43322833 T>C maps to NM_014345.2 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr6:49704205 A>G maps to NM_001190986.1 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr6:49704205 A>G maps to NM_001190986.1 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr6:71232223 A>G maps to NM_001162529.1 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr6:71232223 A>G maps to NM_001162529.1 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr6:100901655 C>T maps to ENST00000262901 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr6:100901655 C>T maps to ENST00000262901 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr6:134638657 T>C did not map to a codon.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr6:134638657 T>C did not map to a codon.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr7:12258147 G>A did not map to a codon.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr7:12258147 G>A did not map to a codon.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr7:43581557 A>G maps to NM_015052.3 L1403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr7:43581557 A>G maps to NM_015052.3 L1403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr9:77370355 G>A maps to NM_017662.4 Q1607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr9:77370355 G>A maps to NM_017662.4 Q1607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr9:114305146 C>T maps to NM_133464.2 F644F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr9:114305146 C>T maps to NM_133464.2 F644F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr9:126137516 C>T maps to NM_173689.5 P1176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr9:126137516 C>T maps to NM_173689.5 P1176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr9:139399999 C>A maps to NM_017617.3 E1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chr9:139399999 C>A maps to NM_017617.3 E1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chrX:70604856 A>G maps to ENST00000449580 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7377-01A-11D-2012-08 chrX:70604856 A>G maps to ENST00000449580 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr1:112303129 G>A maps to NM_007204.4 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr1:112303129 G>A maps to NM_007204.4 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr1:114215338 A>G maps to NM_001142782.1 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr1:114215338 A>G maps to NM_001142782.1 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr10:48388750 C>T maps to NM_002900.2 V709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr10:48388750 C>T maps to NM_002900.2 V709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr10:98743186 T>A maps to NM_015652.2 A680A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr10:98743186 T>A maps to NM_015652.2 A680A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr10:103558655 C>T maps to NM_012215.3 W584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr10:103558655 C>T maps to NM_012215.3 W584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr10:116593010 C>T maps to NM_020940.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr10:116593010 C>T maps to NM_020940.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr10:129913711 T>C maps to NM_002417.4 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr10:129913711 T>C maps to NM_002417.4 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr11:5509983 C>T maps to NM_001005163.2 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr11:5509983 C>T maps to NM_001005163.2 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr11:6452482 C>T maps to NM_000613.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr11:6452482 C>T maps to NM_000613.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr11:47298326 G>C maps to NM_003682.3 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr11:47298326 G>C maps to NM_003682.3 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr11:108380961 G>A maps to NM_015065.2 L1758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr11:108380961 G>A maps to NM_015065.2 L1758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr12:11082883 C>T maps to NM_001110213.1 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr12:11082883 C>T maps to NM_001110213.1 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr12:54110136 C>T maps to NM_020898.2 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr12:54110136 C>T maps to NM_020898.2 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr12:112506763 T>A maps to NM_024953.3 K357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr12:112506763 T>A maps to NM_024953.3 K357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr12:118406029 C>A maps to ENST00000339824 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr12:118406029 C>A maps to ENST00000339824 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr12:124862848 C>A maps to NM_006312.4 E701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr12:124862848 C>A maps to NM_006312.4 E701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr13:49027133 A>T maps to NM_000321.2 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr13:49027133 A>T maps to NM_000321.2 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr14:19566009 A>T did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr14:19566009 A>T did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr14:29237756 G>A maps to NM_005249.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr14:29237756 G>A maps to NM_005249.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr14:30046527 G>T maps to NM_002742.2 I885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr14:30046527 G>T maps to NM_002742.2 I885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr14:64989073 C>T maps to NM_001123329.1 Y284Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr14:64989073 C>T maps to NM_001123329.1 Y284Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr14:67843301 A>C maps to NM_004094.4 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr14:67843301 A>C maps to NM_004094.4 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr15:48760183 C>G maps to NM_000138.4 L1566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr15:48760183 C>G maps to NM_000138.4 L1566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr15:51031994 A>G maps to NM_032802.3 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr15:51031994 A>G maps to NM_032802.3 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr15:91346817 C>T maps to NM_000057.2 A1142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr15:91346817 C>T maps to NM_000057.2 A1142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr16:3646277 C>T maps to NM_032444.2 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr16:3646277 C>T maps to NM_032444.2 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr16:19047108 G>A maps to NM_024847.3 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr16:19047108 G>A maps to NM_024847.3 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr16:20439132 C>A maps to NM_017888.2 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr16:20439132 C>A maps to NM_017888.2 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr16:49764835 C>T maps to NM_015069.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr16:49764835 C>T maps to NM_015069.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr17:4647996 C>G maps to NM_001136046.1 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr17:4647996 C>G maps to NM_001136046.1 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr17:44110823 C>T maps to NM_015443.3 W890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr17:44110823 C>T maps to NM_015443.3 W890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr17:58329764 C>T maps to NM_032582.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr17:58329764 C>T maps to NM_032582.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr17:79658577 G>A maps to NM_004712.4 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr17:79658577 G>A maps to NM_004712.4 E213E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr18:14537868 G>T maps to ENST00000444806 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr18:14537868 G>T maps to ENST00000444806 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr18:30350278 C>T maps to NM_020805.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr18:30350278 C>T maps to NM_020805.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr19:9085507 G>A maps to NM_024690.2 Q2103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr19:9085507 G>A maps to NM_024690.2 Q2103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr19:10129434 G>T maps to NM_015725.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr19:10129434 G>T maps to NM_015725.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr19:12763059 G>A maps to NM_000528.3 N651N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr19:12763059 G>A maps to NM_000528.3 N651N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr19:19790617 A>C maps to NM_033204.2 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr19:19790617 A>C maps to NM_033204.2 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr19:57648259 C>T maps to NM_052882.1 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr19:57648259 C>T maps to NM_052882.1 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr2:212568851 G>A maps to NM_005235.2 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr2:212568851 G>A maps to NM_005235.2 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr2:237172796 G>A maps to NM_212556.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr2:237172796 G>A maps to NM_212556.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr20:42825850 C>T maps to NM_016470.6 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr20:42825850 C>T maps to NM_016470.6 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr22:40815259 A>G maps to NM_020831.3 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr22:40815259 A>G maps to NM_020831.3 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr22:50439547 C>T maps to NM_001001694.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr22:50439547 C>T maps to NM_001001694.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr3:57898144 C>T maps to ENST00000428312 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr3:57898144 C>T maps to ENST00000428312 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr4:4864758 G>T maps to NM_002448.3 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr4:4864758 G>T maps to NM_002448.3 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr4:126241669 C>T maps to NM_024582.4 N1368N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr4:126241669 C>T maps to NM_024582.4 N1368N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr4:177081213 G>A maps to NM_170710.4 V889V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr4:177081213 G>A maps to NM_170710.4 V889V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr5:156668656 C>T maps to NM_005546.3 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr5:156668656 C>T maps to NM_005546.3 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr6:40399667 G>A maps to NM_020737.1 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr6:40399667 G>A maps to NM_020737.1 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr6:64422706 G>A maps to NM_015153.2 E1741E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr6:64422706 G>A maps to NM_015153.2 E1741E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr7:50121442 C>G maps to NM_007009.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr7:50121442 C>G maps to NM_007009.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr8:70476366 C>T maps to NM_001128206.1 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr8:70476366 C>T maps to NM_001128206.1 Q53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr8:91929758 A>T maps to NM_022351.4 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr8:91929758 A>T maps to NM_022351.4 R133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr8:143999223 C>T maps to NM_000498.3 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr8:143999223 C>T maps to NM_000498.3 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr8:145012831 G>T maps to NM_201380.2 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr8:145012831 G>T maps to NM_201380.2 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr9:15199905 G>A maps to NM_152574.2 N259N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr9:15199905 G>A maps to NM_152574.2 N259N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr9:35658693 C>G maps to NM_174923.2 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr9:35658693 C>G maps to NM_174923.2 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chrX:14861943 A>C maps to NM_152633.2 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chrX:14861943 A>C maps to NM_152633.2 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chrX:37431411 A>T maps to NM_001170331.1 K97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chrX:37431411 A>T maps to NM_001170331.1 K97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chrX:37431413 G>A maps to NM_001170331.1 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chrX:37431413 G>A maps to NM_001170331.1 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chrX:48564735 C>A maps to NM_003173.2 Y303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chrX:48564735 C>A maps to NM_003173.2 Y303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chrX:101095786 G>C maps to ENST00000263032 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chrX:101095786 G>C maps to ENST00000263032 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chrX:102337968 C>T maps to NM_022052.1 Q218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chrX:102337968 C>T maps to NM_022052.1 Q218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chrX:151092702 C>G maps to ENST00000427663 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chrX:151092702 C>G maps to ENST00000427663 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chrX:154159319 T>G maps to NM_000132.3 A915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chrX:154159319 T>G maps to NM_000132.3 A915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr1:33745944 C>T maps to NM_152493.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr1:33745944 C>T maps to NM_152493.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr1:78392265 C>G maps to NM_144573.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr1:78392265 C>G maps to NM_144573.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr1:247201302 G>A maps to NM_033213.3 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr1:247201302 G>A maps to NM_033213.3 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr10:71258082 G>A maps to NM_012339.3 Q167Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr10:71258082 G>A maps to NM_012339.3 Q167Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr12:475138 G>C maps to NM_001042603.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr12:475138 G>C maps to NM_001042603.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr13:37439826 G>A maps to NM_001127217.2 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr13:37439826 G>A maps to NM_001127217.2 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr13:109661379 T>C maps to NM_015011.1 L838L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr13:109661379 T>C maps to NM_015011.1 L838L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr16:396962 G>A maps to NM_003502.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr16:396962 G>A maps to NM_003502.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr16:20371928 C>T maps to NM_174924.1 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr16:20371928 C>T maps to NM_174924.1 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr17:7951078 G>A maps to NM_001141.2 W566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr17:7951078 G>A maps to NM_001141.2 W566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr19:9048093 G>T maps to NM_024690.2 T11179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr19:9048093 G>T maps to NM_024690.2 T11179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr19:14069866 T>C maps to NM_138353.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr19:14069866 T>C maps to NM_138353.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr19:56693616 C>T maps to NM_033106.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr19:56693616 C>T maps to NM_033106.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr2:27800114 G>T maps to NM_032266.3 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr2:27800114 G>T maps to NM_032266.3 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr2:54081572 G>A maps to NM_006794.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr2:54081572 G>A maps to NM_006794.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr2:133174855 T>C maps to NM_001508.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr2:133174855 T>C maps to NM_001508.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr2:160690587 G>A maps to NM_001198759.1 Q1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr2:160690587 G>A maps to NM_001198759.1 Q1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr2:220422981 G>A maps to NM_015311.2 H1142H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr2:220422981 G>A maps to NM_015311.2 H1142H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr22:46776785 C>T maps to NM_014246.1 P2385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr22:46776785 C>T maps to NM_014246.1 P2385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr3:174974309 G>A maps to NM_207015.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr3:174974309 G>A maps to NM_207015.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr4:8456492 C>T maps to NM_152544.2 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr4:8456492 C>T maps to NM_152544.2 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr5:13919308 C>T maps to NM_001369.2 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr5:13919308 C>T maps to NM_001369.2 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr5:140683342 G>A maps to NM_031947.2 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr5:140683342 G>A maps to NM_031947.2 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr5:153432558 C>T maps to NM_005927.4 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr5:153432558 C>T maps to NM_005927.4 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr6:30856981 G>A maps to NM_013994.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr6:30856981 G>A maps to NM_013994.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr7:23825152 C>T maps to NM_031414.3 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr7:23825152 C>T maps to NM_031414.3 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr7:156762309 C>T maps to NM_138400.1 H832H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr7:156762309 C>T maps to NM_138400.1 H832H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr8:100147901 C>T maps to NM_017890.3 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr8:100147901 C>T maps to NM_017890.3 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr9:124522453 C>T maps to ENST00000408936 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chr9:124522453 C>T maps to ENST00000408936 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chrX:150832807 C>T maps to NM_173493.2 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7380-01A-11D-2012-08 chrX:150832807 C>T maps to NM_173493.2 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr1:19577910 A>G maps to NM_015047.1 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr1:19577910 A>G maps to NM_015047.1 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr1:237961366 C>T maps to NM_001035.2 R4663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr1:237961366 C>T maps to NM_001035.2 R4663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr10:62648570 G>A maps to NM_014836.4 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr10:62648570 G>A maps to NM_014836.4 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr12:57867439 G>C maps to ENST00000393797 S747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr12:57867439 G>C maps to ENST00000393797 S747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr13:113508637 C>T maps to NM_032189.3 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr13:113508637 C>T maps to NM_032189.3 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr15:93518122 C>A maps to NM_001271.3 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr15:93518122 C>A maps to NM_001271.3 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr17:10354167 G>A maps to NM_017533.2 Q1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr17:10354167 G>A maps to NM_017533.2 Q1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr18:5489116 C>T maps to NM_012307.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr18:5489116 C>T maps to NM_012307.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr18:48573553 G>A maps to NM_005359.5 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr18:48573553 G>A maps to NM_005359.5 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr19:4847852 C>T maps to NM_005817.4 Q228Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr19:4847852 C>T maps to NM_005817.4 Q228Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr19:8551951 C>T maps to NM_005968.3 N674N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr19:8551951 C>T maps to NM_005968.3 N674N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr19:13414686 G>A maps to NM_023035.2 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr19:13414686 G>A maps to NM_023035.2 G667G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr19:35173683 G>A maps to ENST00000221282 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr19:35173683 G>A maps to ENST00000221282 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr3:58555542 C>G maps to ENST00000474531 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr3:58555542 C>G maps to ENST00000474531 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr3:110852575 C>T maps to NM_015480.1 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr3:110852575 C>T maps to NM_015480.1 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr4:129864210 C>T maps to NM_144643.2 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr4:129864210 C>T maps to NM_144643.2 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr4:129873943 C>A maps to NM_144643.2 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr4:129873943 C>A maps to NM_144643.2 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr5:33624345 C>T maps to NM_030955.2 K711K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr5:33624345 C>T maps to NM_030955.2 K711K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr5:41008748 C>T maps to ENST00000296803 V1190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr5:41008748 C>T maps to ENST00000296803 V1190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr5:167689097 C>G maps to NM_001122679.1 A2527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr5:167689097 C>G maps to NM_001122679.1 A2527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr6:139101030 C>T maps to NM_015439.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr6:139101030 C>T maps to NM_015439.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr7:83014671 G>A maps to NM_012431.2 R605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr7:83014671 G>A maps to NM_012431.2 R605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr7:99117509 C>A maps to NM_014569.3 S205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr7:99117509 C>A maps to NM_014569.3 S205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr7:123142650 C>T maps to NM_178827.4 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr7:123142650 C>T maps to NM_178827.4 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr8:21843103 G>A maps to ENST00000434536 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr8:21843103 G>A maps to ENST00000434536 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr8:103305834 G>A maps to NM_015902.4 S1529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr8:103305834 G>A maps to NM_015902.4 S1529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr8:140744266 G>A maps to NM_031466.5 H1176H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr8:140744266 G>A maps to NM_031466.5 H1176H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr8:144940689 G>A maps to NM_031308.1 S2244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr8:144940689 G>A maps to NM_031308.1 S2244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr9:35618374 G>A did not map to a codon.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr9:35618374 G>A did not map to a codon.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr9:90321942 G>A maps to NM_004938.2 P1319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr9:90321942 G>A maps to NM_004938.2 P1319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr9:100331210 G>A maps to NM_003275.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr9:100331210 G>A maps to NM_003275.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr9:100331219 G>A maps to NM_003275.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7382-01A-11D-2129-08 chr9:100331219 G>A maps to NM_003275.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr1:33363921 T>A did not map to a codon.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr1:33363921 T>A did not map to a codon.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr1:59042501 G>A maps to NM_002353.2 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr1:59042501 G>A maps to NM_002353.2 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr1:114397602 G>A maps to NM_015967.5 D203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr1:114397602 G>A maps to NM_015967.5 D203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr1:176738745 G>T maps to NM_020318.2 E1443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr1:176738745 G>T maps to NM_020318.2 E1443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr1:247201494 A>G maps to NM_033213.3 H142H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr1:247201494 A>G maps to NM_033213.3 H142H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr11:57080222 C>A maps to NM_033396.2 E647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr11:57080222 C>A maps to NM_033396.2 E647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr11:61505661 C>T maps to NM_006133.2 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr11:61505661 C>T maps to NM_006133.2 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr11:65417518 G>T maps to NM_153253.29 E949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr11:65417518 G>T maps to NM_153253.29 E949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr12:6753640 C>T maps to NM_032489.2 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr12:6753640 C>T maps to NM_032489.2 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr12:11421067 G>A maps to NM_006249.4 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr12:11421067 G>A maps to NM_006249.4 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr12:11545925 A>G maps to NM_006248.3 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr12:11545925 A>G maps to NM_006248.3 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr12:100728041 G>A maps to NM_017988.4 Q620Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr12:100728041 G>A maps to NM_017988.4 Q620Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr13:33091953 G>T maps to NM_014887.2 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr13:33091953 G>T maps to NM_014887.2 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr14:93176021 G>A maps to NM_005606.6 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr14:93176021 G>A maps to NM_005606.6 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr14:96851861 G>A maps to NM_016472.3 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr14:96851861 G>A maps to NM_016472.3 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr16:20559464 C>T maps to NM_182617.3 E339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr16:20559464 C>T maps to NM_182617.3 E339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr16:89986163 G>A maps to ENST00000304984 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr16:89986163 G>A maps to ENST00000304984 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr17:7576851 C>T did not map to a codon.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr17:7576851 C>T did not map to a codon.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr17:65104672 C>T maps to NM_014877.3 P1553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr17:65104672 C>T maps to NM_014877.3 P1553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr17:73725496 C>T maps to NM_001005619.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr17:73725496 C>T maps to NM_001005619.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr18:57569916 G>A maps to ENST00000269518 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr18:57569916 G>A maps to ENST00000269518 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr19:11537571 C>T maps to NM_145045.4 K215K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr19:11537571 C>T maps to NM_145045.4 K215K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr19:14521048 C>A maps to ENST00000451994 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr19:14521048 C>A maps to ENST00000451994 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr19:17411759 G>A maps to NM_024527.4 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr19:17411759 G>A maps to NM_024527.4 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr2:17697543 A>G maps to NM_001099218.2 C713C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr2:17697543 A>G maps to NM_001099218.2 C713C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr21:40650699 G>A maps to NM_018963.3 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr21:40650699 G>A maps to NM_018963.3 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr3:170078019 C>T did not map to a codon.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr3:170078019 C>T did not map to a codon.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr3:183381263 G>A maps to NM_017644.3 E313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr3:183381263 G>A maps to NM_017644.3 E313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr5:16674966 C>T maps to NM_012334.2 L1653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr5:16674966 C>T maps to NM_012334.2 L1653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr5:140255326 C>A maps to NM_018903.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr5:140255326 C>A maps to NM_018903.2 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr5:154183810 C>T maps to ENST00000377643 S830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr5:154183810 C>T maps to ENST00000377643 S830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr6:45459774 C>A maps to ENST00000359524 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr6:45459774 C>A maps to ENST00000359524 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr6:153043079 C>T maps to NM_025107.2 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr6:153043079 C>T maps to NM_025107.2 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr7:50611623 C>A maps to NM_000790.3 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr7:50611623 C>A maps to NM_000790.3 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr7:89861766 T>G maps to NM_152999.3 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr7:89861766 T>G maps to NM_152999.3 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr8:53062327 A>T maps to NM_014682.2 Y672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr8:53062327 A>T maps to NM_014682.2 Y672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr8:77764889 G>A maps to NM_024721.4 A1911A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr8:77764889 G>A maps to NM_024721.4 A1911A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr9:6587231 G>A maps to NM_000170.2 Q587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr9:6587231 G>A maps to NM_000170.2 Q587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chrX:84585989 G>A maps to ENST00000373145 H273H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chrX:84585989 G>A maps to ENST00000373145 H273H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chrX:107909816 T>C maps to ENST00000328300 G1182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chrX:107909816 T>C maps to ENST00000328300 G1182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr1:149761631 G>A maps to NM_000566.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr1:149761631 G>A maps to NM_000566.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr1:152191392 G>T maps to NM_001009931.1 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr1:152191392 G>T maps to NM_001009931.1 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr1:214478568 A>C maps to NM_020197.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr1:214478568 A>C maps to NM_020197.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr11:78413295 G>A maps to NM_001098816.2 D1454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr11:78413295 G>A maps to NM_001098816.2 D1454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr12:68724992 A>G maps to NM_017440.4 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr12:68724992 A>G maps to NM_017440.4 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr15:42111557 G>A maps to NM_001128608.1 K808K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr15:42111557 G>A maps to NM_001128608.1 K808K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr15:85341885 C>G maps to NM_014630.2 S935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr15:85341885 C>G maps to NM_014630.2 S935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr16:29888271 C>T did not map to a codon.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr16:29888271 C>T did not map to a codon.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr19:10742816 C>T maps to NM_020428.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr19:10742816 C>T maps to NM_020428.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr19:54782208 G>C maps to ENST00000391747 S405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr19:54782208 G>C maps to ENST00000391747 S405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr3:52544477 T>C maps to NM_015136.2 G914G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr3:52544477 T>C maps to NM_015136.2 G914G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr4:71467196 A>G maps to NM_016519.4 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr4:71467196 A>G maps to NM_016519.4 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr5:176687120 C>T maps to NM_022455.4 R1700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr5:176687120 C>T maps to NM_022455.4 R1700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr6:42689523 G>A maps to NM_000322.4 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr6:42689523 G>A maps to NM_000322.4 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr6:43472752 G>A maps to NM_001146016.1 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr6:43472752 G>A maps to NM_001146016.1 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr7:6226734 C>T maps to ENST00000396741 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chr7:6226734 C>T maps to ENST00000396741 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chrX:69458122 C>T maps to NM_001013579.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7385-01A-11D-2012-08 chrX:69458122 C>T maps to NM_001013579.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:6738498 G>A maps to NM_018198.3 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:6738498 G>A maps to NM_018198.3 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:9067372 C>T maps to NM_207420.2 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:9067372 C>T maps to NM_207420.2 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:16273490 G>C maps to ENST00000375733 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:16273490 G>C maps to ENST00000375733 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:32165442 C>T maps to NM_001856.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:32165442 C>T maps to NM_001856.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:38345770 G>A maps to ENST00000373026 D589D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:38345770 G>A maps to ENST00000373026 D589D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:44422117 C>T maps to NM_014652.3 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:44422117 C>T maps to NM_014652.3 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:45480409 C>A maps to NM_000374.4 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:45480409 C>A maps to NM_000374.4 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:45797202 G>A maps to NM_001128425.1 F404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:45797202 G>A maps to NM_001128425.1 F404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:176740226 C>T maps to NM_020318.2 L1542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:176740226 C>T maps to NM_020318.2 L1542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:200880919 G>A maps to NM_018265.2 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr1:200880919 G>A maps to NM_018265.2 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr10:88946847 G>A maps to ENST00000298786 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr10:88946847 G>A maps to ENST00000298786 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr10:105362899 G>C maps to ENST00000369774 S692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr10:105362899 G>C maps to ENST00000369774 S692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr11:1579115 G>A maps to NM_004420.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr11:1579115 G>A maps to NM_004420.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr11:64521766 C>G maps to NM_005609.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr11:64521766 C>G maps to NM_005609.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr12:53849782 G>T maps to NM_005016.5 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr12:53849782 G>T maps to NM_005016.5 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr12:105568150 G>A maps to NM_018171.3 Q646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr12:105568150 G>A maps to NM_018171.3 Q646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr12:111956092 G>A maps to NM_002973.3 F535F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr12:111956092 G>A maps to NM_002973.3 F535F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr14:23897711 C>T maps to NM_000257.2 E525E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr14:23897711 C>T maps to NM_000257.2 E525E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr14:102476267 C>T maps to NM_001376.4 Y2022Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr14:102476267 C>T maps to NM_001376.4 Y2022Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr15:48056144 G>C maps to NM_153618.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr15:48056144 G>C maps to NM_153618.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr16:49672762 G>A maps to NM_015069.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr16:49672762 G>A maps to NM_015069.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr16:66562952 C>T maps to ENST00000299697 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr16:66562952 C>T maps to ENST00000299697 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr16:72984802 C>T maps to NM_006885.3 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr16:72984802 C>T maps to NM_006885.3 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr17:4535216 G>A maps to NM_001140.3 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr17:4535216 G>A maps to NM_001140.3 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr17:39659615 G>A maps to NM_153490.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr17:39659615 G>A maps to NM_153490.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr17:79663006 C>T maps to NM_004712.4 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr17:79663006 C>T maps to NM_004712.4 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr19:6697748 G>A maps to NM_000064.2 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr19:6697748 G>A maps to NM_000064.2 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr19:10415871 G>A maps to NM_001103167.1 Y237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr19:10415871 G>A maps to NM_001103167.1 Y237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr19:11665078 G>A maps to NM_032377.3 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr19:11665078 G>A maps to NM_032377.3 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr19:50042434 C>T maps to NM_020650.2 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr19:50042434 C>T maps to NM_020650.2 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr2:108487256 C>T maps to NM_182588.2 Q933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr2:108487256 C>T maps to NM_182588.2 Q933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr2:166615259 G>A maps to NM_004482.3 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr2:166615259 G>A maps to NM_004482.3 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr2:169023848 G>A maps to NM_013233.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr2:169023848 G>A maps to NM_013233.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr2:170101260 C>T maps to NM_004525.2 K1124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr2:170101260 C>T maps to NM_004525.2 K1124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr2:222298866 G>A maps to NM_004438.3 Q831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr2:222298866 G>A maps to NM_004438.3 Q831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr20:23586432 G>C maps to NM_001008693.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr20:23586432 G>C maps to NM_001008693.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr3:133368366 G>C maps to NM_007027.3 S455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr3:133368366 G>C maps to NM_007027.3 S455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr3:142241602 G>A maps to NM_001184.3 S1411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr3:142241602 G>A maps to NM_001184.3 S1411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr3:155200324 G>A maps to ENST00000340059 L1172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr3:155200324 G>A maps to ENST00000340059 L1172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr3:185882739 G>A maps to NM_001346.2 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr3:185882739 G>A maps to NM_001346.2 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr3:186358275 C>A maps to NM_014375.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr3:186358275 C>A maps to NM_014375.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr3:186793539 C>T maps to NM_003032.2 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr3:186793539 C>T maps to NM_003032.2 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr3:197665629 C>A maps to NM_001134435.1 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr3:197665629 C>A maps to NM_001134435.1 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:957072 C>T maps to NM_001347.2 A580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:957072 C>T maps to NM_001347.2 A580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:2242703 G>C did not map to a codon.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:2242703 G>C did not map to a codon.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:3768938 C>T maps to NM_000683.3 C202C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:3768938 C>T maps to NM_000683.3 C202C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:39276494 C>T maps to NM_025132.3 F1211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:39276494 C>T maps to NM_025132.3 F1211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:83838783 G>C maps to NM_024672.4 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:83838783 G>C maps to NM_024672.4 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:89652579 C>G did not map to a codon.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:89652579 C>G did not map to a codon.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:122068284 T>C maps to ENST00000509841 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:122068284 T>C maps to ENST00000509841 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:187532589 G>C maps to ENST00000260147 S3271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:187532589 G>C maps to ENST00000260147 S3271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr5:40747076 G>C maps to NM_012382.2 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr5:40747076 G>C maps to NM_012382.2 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr5:72798853 G>C maps to NM_001037637.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr5:72798853 G>C maps to NM_001037637.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr5:112256897 G>C maps to NM_005669.4 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr5:112256897 G>C maps to NM_005669.4 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr5:118832265 G>C maps to NM_000414.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr5:118832265 G>C maps to NM_000414.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr5:140779484 C>T maps to NM_018925.2 N597N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr5:140779484 C>T maps to NM_018925.2 N597N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr5:141019744 G>A maps to NM_173828.4 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr5:141019744 G>A maps to NM_173828.4 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr6:56374647 G>A maps to ENST00000361203 I6057I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr6:56374647 G>A maps to ENST00000361203 I6057I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr7:31683299 G>A maps to NM_194300.2 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr7:31683299 G>A maps to NM_194300.2 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr7:50513305 C>T maps to NM_022116.3 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr7:50513305 C>T maps to NM_022116.3 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr7:89939441 C>T maps to NM_001039706.2 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr7:89939441 C>T maps to NM_001039706.2 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr7:106826263 C>T maps to NM_012257.3 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr7:106826263 C>T maps to NM_012257.3 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr7:146536830 C>T maps to NM_014141.5 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr7:146536830 C>T maps to NM_014141.5 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr8:42038170 G>A maps to NM_000930.3 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr8:42038170 G>A maps to NM_000930.3 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr8:48842537 C>A maps to NM_006904.6 E643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr8:48842537 C>A maps to NM_006904.6 E643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr8:92972553 C>T maps to NM_175634.2 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr8:92972553 C>T maps to NM_175634.2 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr8:122626423 C>T maps to NM_005328.2 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr8:122626423 C>T maps to NM_005328.2 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr8:144899259 C>T maps to NM_078480.1 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr8:144899259 C>T maps to NM_078480.1 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr9:21971027 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr9:21971027 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr9:115422153 C>T maps to NM_133465.2 F652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr9:115422153 C>T maps to NM_133465.2 F652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chrX:27999310 C>G maps to NM_001017930.1 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chrX:27999310 C>G maps to NM_001017930.1 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chrX:50377068 G>A maps to NM_020717.3 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chrX:50377068 G>A maps to NM_020717.3 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chrX:107169396 G>A maps to NM_012216.3 E557E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chrX:107169396 G>A maps to NM_012216.3 E557E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chrX:148059933 G>A maps to NM_002025.3 L1173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chrX:148059933 G>A maps to NM_002025.3 L1173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:7999953 C>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:7999953 C>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:11334043 G>C maps to NM_013319.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:11334043 G>C maps to NM_013319.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:24137223 A>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:24137223 A>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:26691025 G>C maps to ENST00000436292 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:26691025 G>C maps to ENST00000436292 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:67558778 G>C maps to NM_001013674.1 S371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:67558778 G>C maps to NM_001013674.1 S371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:85733495 C>T maps to NM_003921.4 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:85733495 C>T maps to NM_003921.4 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:94650454 C>T maps to NM_004815.3 E694E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:94650454 C>T maps to NM_004815.3 E694E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:152278664 T>C maps to NM_002016.1 G2899G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:152278664 T>C maps to NM_002016.1 G2899G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:152284281 G>C maps to NM_002016.1 S1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:152284281 G>C maps to NM_002016.1 S1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:152681604 C>A maps to NM_178356.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:152681604 C>A maps to NM_178356.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:155924707 G>A maps to NM_001162383.1 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:155924707 G>A maps to NM_001162383.1 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:157545496 C>A maps to NM_031282.2 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:157545496 C>A maps to NM_031282.2 E485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:158153925 C>T maps to NM_001766.3 Q332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:158153925 C>T maps to NM_001766.3 Q332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:158812149 C>A maps to NM_002432.1 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:158812149 C>A maps to NM_002432.1 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:159410396 G>C maps to NM_012351.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:159410396 G>C maps to NM_012351.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:160098578 C>A maps to NM_000702.3 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:160098578 C>A maps to NM_000702.3 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:167095718 C>T maps to NM_001080426.1 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:167095718 C>T maps to NM_001080426.1 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:170961322 G>A maps to NM_001163629.1 W349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:170961322 G>A maps to NM_001163629.1 W349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:179398720 C>T maps to NM_144696.4 Y433Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:179398720 C>T maps to NM_144696.4 Y433Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:183230438 C>G did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:183230438 C>G did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:185833651 G>A maps to NM_031935.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:185833651 G>A maps to NM_031935.2 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:198682088 A>G maps to ENST00000271610 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:198682088 A>G maps to ENST00000271610 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:200182930 C>A maps to NM_001105517.1 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:200182930 C>A maps to NM_001105517.1 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:214171245 C>A maps to NM_002763.3 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:214171245 C>A maps to NM_002763.3 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:223933089 C>G maps to NM_001748.4 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:223933089 C>G maps to NM_001748.4 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:228346340 G>C maps to NM_020435.2 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:228346340 G>C maps to NM_020435.2 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:237777905 T>C maps to NM_001035.2 Y1826Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:237777905 T>C maps to NM_001035.2 Y1826Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:240492683 C>G maps to ENST00000406993 V1594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:240492683 C>G maps to ENST00000406993 V1594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:241798316 G>C maps to NM_001821.3 S251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:241798316 G>C maps to NM_001821.3 S251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:248437008 G>T maps to NM_001004695.1 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr1:248437008 G>T maps to NM_001004695.1 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr10:61592412 T>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr10:61592412 T>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr10:68687294 C>G maps to NM_178011.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr10:68687294 C>G maps to NM_178011.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr10:79784810 G>A maps to NM_007055.3 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr10:79784810 G>A maps to NM_007055.3 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr10:116853720 C>A maps to NM_207303.2 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr10:116853720 C>A maps to NM_207303.2 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr10:120809437 G>A maps to NM_003750.2 Q845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr10:120809437 G>A maps to NM_003750.2 Q845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr10:121618669 G>T maps to NM_024834.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr10:121618669 G>T maps to NM_024834.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:6129217 C>A maps to NM_001005181.1 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:6129217 C>A maps to NM_001005181.1 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:9090929 C>T maps to ENST00000457346 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:9090929 C>T maps to ENST00000457346 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:46564191 G>A maps to ENST00000458649 Q459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:46564191 G>A maps to ENST00000458649 Q459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:46772904 T>C maps to ENST00000415402 K1771K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:46772904 T>C maps to ENST00000415402 K1771K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:48346906 C>T maps to NM_001004702.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:48346906 C>T maps to NM_001004702.1 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:55371369 C>A maps to NM_001004700.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:55371369 C>A maps to NM_001004700.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:57947761 C>A maps to NM_001005212.3 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:57947761 C>A maps to NM_001005212.3 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:57996164 G>C maps to NM_001004471.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:57996164 G>C maps to NM_001004471.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:65617934 G>A maps to NM_152760.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:65617934 G>A maps to NM_152760.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:69063360 G>T maps to NM_138768.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:69063360 G>T maps to NM_138768.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:78413271 G>T maps to NM_001098816.2 A1462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:78413271 G>T maps to NM_001098816.2 A1462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:85375814 C>G maps to NM_001039618.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:85375814 C>G maps to NM_001039618.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:92523336 G>T maps to ENST00000298047 E1522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:92523336 G>T maps to ENST00000298047 E1522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:93088642 C>T maps to NM_181645.3 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr11:93088642 C>T maps to NM_181645.3 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:6939087 G>C maps to NM_014262.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:6939087 G>C maps to NM_014262.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:7177303 G>T maps to NM_001734.3 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:7177303 G>T maps to NM_001734.3 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:8211439 G>A maps to NM_004054.2 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:8211439 G>A maps to NM_004054.2 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:14959574 T>G maps to NM_001013698.2 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:14959574 T>G maps to NM_001013698.2 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:32260339 G>C maps to NM_001714.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:32260339 G>C maps to NM_001714.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:32793298 G>T maps to NM_139241.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:32793298 G>T maps to NM_139241.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:49434306 G>A maps to NM_003482.3 Q2416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:49434306 G>A maps to NM_003482.3 Q2416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:51584172 T>A maps to NM_002702.3 K255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:51584172 T>A maps to NM_002702.3 K255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:56094760 G>A maps to ENST00000347027 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:56094760 G>A maps to ENST00000347027 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:57929538 C>T maps to ENST00000434715 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:57929538 C>T maps to ENST00000434715 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:69265655 C>G maps to NM_001874.4 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:69265655 C>G maps to NM_001874.4 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:70049560 C>T maps to NM_032735.2 W378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:70049560 C>T maps to NM_032735.2 W378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:78562545 T>A maps to NM_014903.4 L1627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:78562545 T>A maps to NM_014903.4 L1627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:86373114 T>G maps to ENST00000393205 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:86373114 T>G maps to ENST00000393205 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:94694715 G>A maps to NM_005761.1 L1423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:94694715 G>A maps to NM_005761.1 L1423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:101017767 G>C maps to NM_174942.1 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:101017767 G>C maps to NM_174942.1 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:103699897 C>T maps to NM_001099336.1 W162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:103699897 C>T maps to NM_001099336.1 W162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:113614712 C>A maps to NM_001111322.1 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:113614712 C>A maps to NM_001111322.1 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:124221631 G>A maps to NM_012463.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:124221631 G>A maps to NM_012463.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:130912809 C>A maps to NM_015347.4 E759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:130912809 C>A maps to NM_015347.4 E759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:133327232 C>T maps to NM_015114.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr12:133327232 C>T maps to NM_015114.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr13:36744766 T>G maps to ENST00000511166 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr13:36744766 T>G maps to ENST00000511166 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr13:37269081 A>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr13:37269081 A>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr13:38143520 C>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr13:38143520 C>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr13:46542017 C>T maps to ENST00000242848 E1314E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr13:46542017 C>T maps to ENST00000242848 E1314E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr13:86369100 C>A maps to NM_032229.2 E515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr13:86369100 C>A maps to NM_032229.2 E515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr14:30066889 G>A maps to NM_002742.2 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr14:30066889 G>A maps to NM_002742.2 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr14:36988379 G>A maps to NM_001079668.2 H91H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr14:36988379 G>A maps to NM_001079668.2 H91H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr14:50088060 G>A maps to NM_002408.3 W25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr14:50088060 G>A maps to NM_002408.3 W25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr14:51375032 C>A maps to NM_002863.4 E779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr14:51375032 C>A maps to NM_002863.4 E779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr14:59946013 G>A maps to NM_144581.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr14:59946013 G>A maps to NM_144581.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr14:65041171 G>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr14:65041171 G>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr14:74759944 C>A maps to NM_005050.3 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr14:74759944 C>A maps to NM_005050.3 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr15:75977613 C>T maps to NM_001897.4 L1406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr15:75977613 C>T maps to NM_001897.4 L1406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr15:81041862 G>T maps to NM_021214.1 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr15:81041862 G>T maps to NM_021214.1 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr15:92981808 C>T maps to NM_006011.3 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr15:92981808 C>T maps to NM_006011.3 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:1720767 G>C maps to NM_020825.3 S1201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:1720767 G>C maps to NM_020825.3 S1201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:2159506 G>A maps to NM_001009944.2 I1887I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:2159506 G>A maps to NM_001009944.2 I1887I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:3304449 G>A maps to NM_000243.2 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:3304449 G>A maps to NM_000243.2 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:3487314 T>A maps to NM_152457.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:3487314 T>A maps to NM_152457.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:67173917 G>A maps to NM_025187.3 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:67173917 G>A maps to NM_025187.3 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:71015348 C>G maps to NM_032821.2 L1484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:71015348 C>G maps to NM_032821.2 L1484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:72158691 C>A maps to NM_031293.2 E855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:72158691 C>A maps to NM_031293.2 E855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:74716631 C>G maps to NM_152649.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr16:74716631 C>G maps to NM_152649.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:1437392 T>C maps to ENST00000313486 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:1437392 T>C maps to ENST00000313486 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:10406201 A>G maps to NM_005963.3 G988G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:10406201 A>G maps to NM_005963.3 G988G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:27829691 C>G maps to NM_020791.2 S430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:27829691 C>G maps to NM_020791.2 S430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:36484371 C>A maps to ENST00000398597 E1695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:36484371 C>A maps to ENST00000398597 E1695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:36485275 C>A maps to ENST00000398597 G1393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:36485275 C>A maps to ENST00000398597 G1393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:40865278 T>C maps to ENST00000264646 K387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:40865278 T>C maps to ENST00000264646 K387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:45056163 G>T maps to NM_203400.3 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:45056163 G>T maps to NM_203400.3 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:47699429 C>G did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr17:47699429 C>G did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr18:5397175 C>A maps to NM_012307.2 E908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr18:5397175 C>A maps to NM_012307.2 E908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr18:13884800 G>T maps to NM_000529.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr18:13884800 G>T maps to NM_000529.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr18:31323160 C>T maps to NM_030632.1 R1117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr18:31323160 C>T maps to NM_030632.1 R1117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr18:56202140 T>A maps to NM_052947.3 K1760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr18:56202140 T>A maps to NM_052947.3 K1760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:6694460 G>T maps to NM_000064.2 A1045A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:6694460 G>T maps to NM_000064.2 A1045A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:7705801 G>C maps to ENST00000441779 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:7705801 G>C maps to ENST00000441779 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:7810692 C>T maps to NM_021155.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:7810692 C>T maps to NM_021155.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:9048497 G>A maps to NM_024690.2 L11045L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:9048497 G>A maps to NM_024690.2 L11045L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:9297145 C>G maps to NM_175883.2 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:9297145 C>G maps to NM_175883.2 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:14710933 C>T maps to ENST00000417570 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:14710933 C>T maps to ENST00000417570 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:19356186 G>A maps to NM_004386.2 V1186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:19356186 G>A maps to NM_004386.2 V1186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:21991839 C>T maps to NM_003423.2 K333K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:21991839 C>T maps to NM_003423.2 K333K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:22155675 G>C maps to NM_007153.3 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:22155675 G>C maps to NM_007153.3 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:30936466 G>T maps to NM_014717.1 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:30936466 G>T maps to NM_014717.1 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:36018829 C>T maps to NM_001166034.1 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:36018829 C>T maps to NM_001166034.1 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:38692544 G>C maps to NM_015073.1 L1676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:38692544 G>C maps to NM_015073.1 L1676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:40366445 G>A maps to NM_003890.2 F4596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:40366445 G>A maps to NM_003890.2 F4596F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:44661806 G>A maps to NM_006630.2 G546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:44661806 G>A maps to NM_006630.2 G546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:47969075 C>T maps to NM_015063.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:47969075 C>T maps to NM_015063.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:48305448 G>C maps to NM_198479.2 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:48305448 G>C maps to NM_198479.2 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:49912473 G>A maps to NM_144688.4 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:49912473 G>A maps to NM_144688.4 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:50549314 A>C maps to NM_015428.1 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:50549314 A>C maps to NM_015428.1 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:51293712 C>T maps to NM_033068.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:51293712 C>T maps to NM_033068.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:53058025 A>G maps to NM_001039886.3 G619G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:53058025 A>G maps to NM_001039886.3 G619G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:55915772 G>A maps to NM_014501.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr19:55915772 G>A maps to NM_014501.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:21231101 G>A maps to NM_000384.2 Q2880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:21231101 G>A maps to NM_000384.2 Q2880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:26502172 C>T maps to NM_000183.2 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:26502172 C>T maps to NM_000183.2 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:68609700 T>A maps to NM_002664.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:68609700 T>A maps to NM_002664.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:105897017 G>A maps to NM_004257.4 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:105897017 G>A maps to NM_004257.4 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:109988085 G>T maps to NM_001099289.1 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:109988085 G>T maps to NM_001099289.1 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:145147398 C>T maps to NM_014795.3 R1088R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:145147398 C>T maps to NM_014795.3 R1088R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:152138557 C>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:152138557 C>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:160294954 C>G maps to NM_013450.2 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:160294954 C>G maps to NM_013450.2 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:160994113 C>G maps to NM_000888.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:160994113 C>G maps to NM_000888.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:162711548 T>C maps to NM_001178015.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:162711548 T>C maps to NM_001178015.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:169791839 G>T maps to NM_003742.2 P970P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:169791839 G>T maps to NM_003742.2 P970P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:169989113 G>A maps to NM_004525.2 N4566N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:169989113 G>A maps to NM_004525.2 N4566N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:209308193 G>T maps to NM_005048.2 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:209308193 G>T maps to NM_005048.2 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:216904000 G>C maps to NM_018441.5 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:216904000 G>C maps to NM_018441.5 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:219873819 G>A maps to NM_194302.2 D1541D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr2:219873819 G>A maps to NM_194302.2 D1541D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr20:33440232 C>A maps to NM_178026.2 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr20:33440232 C>A maps to NM_178026.2 V476V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CR-7388-01A-11D-2012-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CR-7388-01A-11D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr20:35441118 G>A maps to NM_080627.2 S815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr20:35441118 G>A maps to NM_080627.2 S815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr20:37356753 C>A maps to NM_080552.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr20:37356753 C>A maps to NM_080552.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr21:41719756 A>G maps to NM_001389.3 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr21:41719756 A>G maps to NM_001389.3 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr21:46945760 C>A maps to NM_194255.1 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr21:46945760 C>A maps to NM_194255.1 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr22:36629288 T>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr22:36629288 T>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr22:44340663 C>T maps to NM_025225.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr22:44340663 C>T maps to NM_025225.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:40231678 C>A maps to NM_015460.2 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:40231678 C>A maps to NM_015460.2 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:42793454 C>T maps to NM_144719.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:42793454 C>T maps to NM_144719.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:74350576 G>A maps to NM_020872.1 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:74350576 G>A maps to NM_020872.1 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:87018031 C>A maps to NM_016206.2 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:87018031 C>A maps to NM_016206.2 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:119156655 G>A maps to NM_018266.1 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:119156655 G>A maps to NM_018266.1 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:120998663 G>T maps to NM_014980.2 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:120998663 G>T maps to NM_014980.2 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:121217351 G>A maps to ENST00000393672 Q845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:121217351 G>A maps to ENST00000393672 Q845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:122811250 G>T maps to NM_006810.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:122811250 G>T maps to NM_006810.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:122842956 C>T maps to NM_006810.3 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:122842956 C>T maps to NM_006810.3 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:137803005 G>C maps to NM_173543.2 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:137803005 G>C maps to NM_173543.2 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:139090584 T>C maps to NM_004766.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:139090584 T>C maps to NM_004766.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:147113921 G>C maps to NM_001168379.1 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:147113921 G>C maps to NM_001168379.1 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:156711003 G>T maps to NM_001004316.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:156711003 G>T maps to NM_001004316.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:158399881 T>A maps to ENST00000264263 L586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:158399881 T>A maps to ENST00000264263 L586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:160243623 T>A maps to NM_002268.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:160243623 T>A maps to NM_002268.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:186450367 G>T maps to NM_001102416.2 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr3:186450367 G>T maps to NM_001102416.2 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:52938152 C>A maps to NM_145263.2 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:52938152 C>A maps to NM_145263.2 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:55131136 C>A maps to NM_006206.4 S227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:55131136 C>A maps to NM_006206.4 S227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:70079864 G>T maps to NM_001073.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:70079864 G>T maps to NM_001073.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:95223374 C>T maps to NM_014485.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:95223374 C>T maps to NM_014485.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:96256639 G>T maps to NM_003728.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:96256639 G>T maps to NM_003728.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:106156785 G>T maps to ENST00000513237 G584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:106156785 G>T maps to ENST00000513237 G584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:120240197 A>T maps to NM_000134.3 *133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:120240197 A>T maps to NM_000134.3 *133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:149357049 C>A maps to ENST00000511528 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:149357049 C>A maps to ENST00000511528 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:156289866 T>A maps to NM_001039580.1 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr4:156289866 T>A maps to NM_001039580.1 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:36953854 C>T maps to NM_133433.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:36953854 C>T maps to NM_133433.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:37003450 T>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:37003450 T>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:71482445 C>A maps to NM_005909.3 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:71482445 C>A maps to NM_005909.3 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:127647622 G>C maps to NM_001999.3 P1634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:127647622 G>C maps to NM_001999.3 P1634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:127686625 G>A maps to NM_001999.3 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:127686625 G>A maps to NM_001999.3 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:140215587 G>C maps to NM_018910.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:140215587 G>C maps to NM_018910.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:140554221 G>T maps to NM_018940.2 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:140554221 G>T maps to NM_018940.2 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:140755149 C>A maps to NM_018919.2 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:140755149 C>A maps to NM_018919.2 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:140764244 G>C maps to NM_018920.2 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:140764244 G>C maps to NM_018920.2 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:156770190 G>A maps to NM_001001343.3 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:156770190 G>A maps to NM_001001343.3 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:161119064 C>T maps to NM_000811.2 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr5:161119064 C>T maps to NM_000811.2 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:26271336 G>T maps to NM_003534.2 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:26271336 G>T maps to NM_003534.2 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:27925413 C>A maps to NM_012367.1 Y132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:27925413 C>A maps to NM_012367.1 Y132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:30863277 C>T maps to NM_013994.2 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:30863277 C>T maps to NM_013994.2 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:30878469 C>T maps to NM_001517.4 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:30878469 C>T maps to NM_001517.4 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:32037925 A>C maps to ENST00000375244 P1752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:32037925 A>C maps to ENST00000375244 P1752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:36767802 G>A maps to NM_020939.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:36767802 G>A maps to NM_020939.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:56044742 G>A maps to NM_030820.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:56044742 G>A maps to NM_030820.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:100868713 G>A maps to ENST00000262901 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:100868713 G>A maps to ENST00000262901 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:151939224 A>G maps to ENST00000367290 K704K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:151939224 A>G maps to ENST00000367290 K704K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:152786533 G>C maps to NM_182961.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:152786533 G>C maps to NM_182961.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:152826447 C>A maps to NM_182961.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:152826447 C>A maps to NM_182961.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:158516990 T>C maps to NM_003898.3 N1362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:158516990 T>C maps to NM_003898.3 N1362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:4796622 A>G did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:4796622 A>G did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:21779239 C>T maps to NM_003777.3 V2628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:21779239 C>T maps to NM_003777.3 V2628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:29111997 G>A maps to NM_031311.3 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:29111997 G>A maps to NM_031311.3 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:32908968 T>C maps to NM_015483.2 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:32908968 T>C maps to NM_015483.2 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:37955824 G>T maps to ENST00000223214 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:37955824 G>T maps to ENST00000223214 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:73184250 C>T maps to NM_001306.3 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:73184250 C>T maps to NM_001306.3 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:75189090 G>A maps to NM_005338.4 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:75189090 G>A maps to NM_005338.4 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:80394476 G>C maps to NM_006379.2 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:80394476 G>C maps to NM_006379.2 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:89982158 C>G maps to NM_033107.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:89982158 C>G maps to NM_033107.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:100685078 C>G maps to NM_001040105.1 S3461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:100685078 C>G maps to NM_001040105.1 S3461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:106509406 G>T maps to NM_002649.2 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:106509406 G>T maps to NM_002649.2 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:107340589 C>T maps to NM_000441.1 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:107340589 C>T maps to NM_000441.1 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:141315362 C>A maps to NM_018238.3 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:141315362 C>A maps to NM_018238.3 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:141673225 C>T maps to NM_176817.4 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:141673225 C>T maps to NM_176817.4 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:143701433 G>C maps to NM_001005281.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:143701433 G>C maps to NM_001005281.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:144060359 G>T maps to NM_005435.3 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr7:144060359 G>T maps to NM_005435.3 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:19811806 C>T maps to NM_000237.2 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:19811806 C>T maps to NM_000237.2 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:30702708 C>G maps to NM_031271.3 V1275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:30702708 C>G maps to NM_031271.3 V1275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:48697803 G>A maps to NM_006904.6 F3658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:48697803 G>A maps to NM_006904.6 F3658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:110100016 C>A maps to NM_003301.4 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:110100016 C>A maps to NM_003301.4 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:110420424 C>G maps to ENST00000426474 S654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:110420424 C>G maps to ENST00000426474 S654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:110984838 G>T maps to NM_014379.2 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:110984838 G>T maps to NM_014379.2 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:113562954 G>T maps to NM_198123.1 I1503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:113562954 G>T maps to NM_198123.1 I1503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:139729091 G>A maps to NM_152888.1 G792G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:139729091 G>A maps to NM_152888.1 G792G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:143783129 G>C maps to ENST00000292430 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:143783129 G>C maps to ENST00000292430 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:145773626 G>A maps to NM_025251.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr8:145773626 G>A maps to NM_025251.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:5754838 A>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:5754838 A>T did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:37740291 G>T maps to NM_014907.2 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:37740291 G>T maps to NM_014907.2 A589A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:90536022 C>T maps to NM_001145124.1 Q401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:90536022 C>T maps to NM_001145124.1 Q401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:112899230 A>G maps to NM_007203.4 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:112899230 A>G maps to NM_007203.4 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:121976296 C>G maps to NM_014618.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:121976296 C>G maps to NM_014618.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:123930379 C>T maps to NM_007018.4 Q1951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:123930379 C>T maps to NM_007018.4 Q1951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:125643073 C>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:125643073 C>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:133945218 C>T maps to ENST00000355048 Y1017Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:133945218 C>T maps to ENST00000355048 Y1017Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:139371757 G>A maps to NM_014866.1 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr9:139371757 G>A maps to NM_014866.1 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:18660201 G>T maps to NM_000330.3 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:18660201 G>T maps to NM_000330.3 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:19475137 C>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:19475137 C>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:23749057 G>A maps to NM_001037171.1 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:23749057 G>A maps to NM_001037171.1 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:39932750 G>T maps to NM_001123385.1 G616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:39932750 G>T maps to NM_001123385.1 G616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:48542679 C>A maps to NM_000377.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:48542679 C>A maps to NM_000377.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:48672939 C>A maps to ENST00000444343 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:48672939 C>A maps to ENST00000444343 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:48826246 G>T maps to NM_004979.4 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:48826246 G>T maps to NM_004979.4 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:49142666 G>C maps to NM_033215.4 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:49142666 G>C maps to NM_033215.4 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:50089706 G>A maps to NM_033031.2 Q1237Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:50089706 G>A maps to NM_033031.2 Q1237Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:52844168 G>T maps to NM_130775.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:52844168 G>T maps to NM_130775.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:53571656 G>C maps to ENST00000276009 L3707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:53571656 G>C maps to ENST00000276009 L3707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:54785153 G>T maps to NM_198510.2 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:54785153 G>T maps to NM_198510.2 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:55248197 A>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:55248197 A>C did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:63412058 C>A maps to NM_152424.3 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:63412058 C>A maps to NM_152424.3 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:69719859 T>C maps to ENST00000194900 Y734Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:69719859 T>C maps to ENST00000194900 Y734Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:78010698 C>A maps to NM_005296.2 C111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:78010698 C>A maps to NM_005296.2 C111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:82763400 G>A maps to NM_000307.3 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:82763400 G>A maps to NM_000307.3 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:84362471 C>T maps to NM_001012980.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:84362471 C>T maps to NM_001012980.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:102632527 C>A maps to NM_206915.1 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:102632527 C>A maps to NM_206915.1 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:107977921 G>T maps to NM_003604.2 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:107977921 G>T maps to NM_003604.2 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:112025793 A>G maps to NM_001113490.1 N738N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:112025793 A>G maps to NM_001113490.1 N738N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:119054533 C>T maps to NM_178813.5 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:119054533 C>T maps to NM_178813.5 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:120183196 T>C maps to NM_012084.3 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:120183196 T>C maps to NM_012084.3 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:135961277 G>A maps to NM_002139.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:135961277 G>A maps to NM_002139.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:141291017 C>A maps to NM_016249.3 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:141291017 C>A maps to NM_016249.3 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:153132809 C>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:153132809 C>A did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:153132823 G>C maps to NM_000425.3 V708V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chrX:153132823 G>C maps to NM_000425.3 V708V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr1:113636138 A>T maps to NM_014813.1 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr1:113636138 A>T maps to NM_014813.1 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr1:158639215 T>C maps to NM_003126.2 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr1:158639215 T>C maps to NM_003126.2 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr10:91098945 T>C maps to NM_001549.4 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr10:91098945 T>C maps to NM_001549.4 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr11:56057818 A>G maps to NM_001005199.1 C240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr11:56057818 A>G maps to NM_001005199.1 C240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr11:108348423 T>C maps to NM_153705.4 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr11:108348423 T>C maps to NM_153705.4 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr12:13526326 C>T maps to ENST00000318426 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr12:13526326 C>T maps to ENST00000318426 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr12:53069123 G>A maps to NM_006121.3 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr12:53069123 G>A maps to NM_006121.3 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr12:54063125 C>T did not map to a codon.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr12:54063125 C>T did not map to a codon.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr14:60582437 A>G maps to ENST00000404681 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr14:60582437 A>G maps to ENST00000404681 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr14:95033316 G>A maps to NM_006215.2 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr14:95033316 G>A maps to NM_006215.2 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr15:42701995 C>T maps to NM_000070.2 I668I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr15:42701995 C>T maps to NM_000070.2 I668I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr15:78474319 G>A maps to NM_015162.4 D354D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr15:78474319 G>A maps to NM_015162.4 D354D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr17:26731994 G>A maps to ENST00000440501 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr17:26731994 G>A maps to ENST00000440501 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr18:347015 G>A maps to NM_130386.2 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr18:347015 G>A maps to NM_130386.2 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr18:59928748 A>G maps to NM_020854.3 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr18:59928748 A>G maps to NM_020854.3 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr19:18235531 C>T maps to NM_015016.1 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr19:18235531 C>T maps to NM_015016.1 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr19:42873016 G>A maps to ENST00000251268 G2168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr19:42873016 G>A maps to ENST00000251268 G2168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr19:44739551 T>C maps to NM_182490.1 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr19:44739551 T>C maps to NM_182490.1 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr19:44933968 G>A maps to NM_014518.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr19:44933968 G>A maps to NM_014518.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr2:74688528 C>T maps to NM_006302.2 W796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr2:74688528 C>T maps to NM_006302.2 W796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr2:179404535 T>C maps to NM_133378.4 A30184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr2:179404535 T>C maps to NM_133378.4 A30184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr2:242793392 G>A maps to NM_005018.2 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr2:242793392 G>A maps to NM_005018.2 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr22:40066098 C>A maps to NM_021096.3 I1417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr22:40066098 C>A maps to NM_021096.3 I1417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr3:35732404 T>A maps to ENST00000458225 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr3:35732404 T>A maps to ENST00000458225 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr3:100489650 G>A maps to ENST00000471714 T1550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr3:100489650 G>A maps to ENST00000471714 T1550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr3:164758750 T>G maps to NM_001041.3 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr3:164758750 T>G maps to NM_001041.3 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr4:148800392 G>A maps to NM_024605.3 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr4:148800392 G>A maps to NM_024605.3 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr5:665267 G>A maps to NM_007030.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr5:665267 G>A maps to NM_007030.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr5:13841091 G>A maps to NM_001369.2 L1878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr5:13841091 G>A maps to NM_001369.2 L1878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr5:40681847 C>G maps to NM_000958.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr5:40681847 C>G maps to NM_000958.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr5:78752756 A>G maps to NM_004272.3 H30H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr5:78752756 A>G maps to NM_004272.3 H30H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr5:150275861 A>G maps to NM_001172831.1 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr5:150275861 A>G maps to NM_001172831.1 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr6:44247947 A>T maps to NM_182539.3 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr6:44247947 A>T maps to NM_182539.3 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr6:151121854 G>A maps to NM_001029884.1 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr6:151121854 G>A maps to NM_001029884.1 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr7:57188427 T>A maps to NM_033273.1 K232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr7:57188427 T>A maps to NM_033273.1 K232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr7:73535346 C>T maps to NM_002314.2 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr7:73535346 C>T maps to NM_002314.2 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr7:80091817 C>T maps to NM_001102386.1 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr7:80091817 C>T maps to NM_001102386.1 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr8:37699032 C>T maps to NM_032777.9 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr8:37699032 C>T maps to NM_032777.9 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr8:55533930 G>A maps to NM_006269.1 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr8:55533930 G>A maps to NM_006269.1 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr8:92972687 G>A maps to NM_175634.2 R533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr8:92972687 G>A maps to NM_175634.2 R533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr9:94486930 G>A maps to NM_004560.2 D615D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr9:94486930 G>A maps to NM_004560.2 D615D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr9:106891993 T>C maps to NM_001042550.1 S953S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7389-01A-11D-2012-08 chr9:106891993 T>C maps to NM_001042550.1 S953S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr1:45923295 C>T maps to NM_007170.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr1:45923295 C>T maps to NM_007170.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr1:110882110 G>A maps to NM_022768.4 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr1:110882110 G>A maps to NM_022768.4 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr1:157773647 C>T maps to NM_052938.4 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr1:157773647 C>T maps to NM_052938.4 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr10:6148124 A>G maps to NM_001145547.1 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr10:6148124 A>G maps to NM_001145547.1 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr10:8007659 G>A maps to NM_031923.2 E729E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr10:8007659 G>A maps to NM_031923.2 E729E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr10:16918965 C>T maps to NM_001081.3 P3012P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr10:16918965 C>T maps to NM_001081.3 P3012P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr10:75407450 T>C maps to NM_001114133.1 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr10:75407450 T>C maps to NM_001114133.1 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr10:81058852 C>T maps to NM_020338.3 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr10:81058852 C>T maps to NM_020338.3 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr10:93668074 C>A maps to NM_152429.4 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr10:93668074 C>A maps to NM_152429.4 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr11:5020607 G>A maps to NM_001004755.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr11:5020607 G>A maps to NM_001004755.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr11:6024282 G>A maps to NM_001005179.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr11:6024282 G>A maps to NM_001005179.2 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr11:17428227 C>T maps to ENST00000302539 L1091L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr11:17428227 C>T maps to ENST00000302539 L1091L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr11:65294569 C>T maps to NM_020680.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr11:65294569 C>T maps to NM_020680.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr11:66192178 C>T maps to NM_178864.3 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr11:66192178 C>T maps to NM_178864.3 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr12:3387621 G>A maps to ENST00000407263 W33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr12:3387621 G>A maps to ENST00000407263 W33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr12:27235254 C>G maps to ENST00000398815 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr12:27235254 C>G maps to ENST00000398815 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr14:24030797 G>A maps to NM_003917.2 Q594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr14:24030797 G>A maps to NM_003917.2 Q594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr14:32561107 A>G maps to NM_001030055.1 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr14:32561107 A>G maps to NM_001030055.1 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr15:73925475 G>C maps to NM_012428.3 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr15:73925475 G>C maps to NM_012428.3 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr16:47196539 G>A maps to NM_030790.3 Q497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr16:47196539 G>A maps to NM_030790.3 Q497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr16:57147237 C>T maps to NM_152727.5 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr16:57147237 C>T maps to NM_152727.5 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr16:89351116 G>A maps to NM_013275.4 F611F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr16:89351116 G>A maps to NM_013275.4 F611F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr17:10352201 C>T maps to NM_017533.2 K1448K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr17:10352201 C>T maps to NM_017533.2 K1448K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr17:39580042 C>T maps to NM_003770.4 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr17:39580042 C>T maps to NM_003770.4 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr17:40175776 G>T maps to ENST00000316082 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr17:40175776 G>T maps to ENST00000316082 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr17:56355307 G>A maps to ENST00000340482 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr17:56355307 G>A maps to ENST00000340482 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr17:72588199 G>A maps to NM_152460.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr17:72588199 G>A maps to NM_152460.2 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr17:73235979 G>A maps to NM_138619.2 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr17:73235979 G>A maps to NM_138619.2 A491A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CR-7390-01A-11D-2012-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CR-7390-01A-11D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr19:21992241 C>A maps to NM_003423.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr19:21992241 C>A maps to NM_003423.2 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr19:38600874 G>A maps to NM_015073.1 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr19:38600874 G>A maps to NM_015073.1 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr19:56490772 C>T maps to NM_176811.2 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr19:56490772 C>T maps to NM_176811.2 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr2:97377726 G>A maps to NM_001142292.1 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr2:97377726 G>A maps to NM_001142292.1 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr2:119600537 G>T maps to NM_001426.3 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr2:119600537 G>T maps to NM_001426.3 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr2:160673379 G>C maps to NM_001198759.1 L1439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr2:160673379 G>C maps to NM_001198759.1 L1439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr2:179539080 T>G maps to NM_133378.4 P10255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr2:179539080 T>G maps to NM_133378.4 P10255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr20:2640752 G>A maps to NM_006899.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr20:2640752 G>A maps to NM_006899.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr20:31604855 G>C maps to NM_025227.1 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr20:31604855 G>C maps to NM_025227.1 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr3:113098398 C>G did not map to a codon.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr3:113098398 C>G did not map to a codon.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr3:119133481 G>A maps to NM_020754.2 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr3:119133481 G>A maps to NM_020754.2 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr3:125828901 G>A maps to ENST00000273450 T754T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr3:125828901 G>A maps to ENST00000273450 T754T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr3:125833453 C>T maps to ENST00000273450 G686G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr3:125833453 C>T maps to ENST00000273450 G686G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr3:147114161 G>C maps to NM_001168379.1 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr3:147114161 G>C maps to NM_001168379.1 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr3:165547585 G>A maps to NM_000055.2 N412N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr3:165547585 G>A maps to NM_000055.2 N412N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr4:25258232 G>A maps to NM_018323.3 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr4:25258232 G>A maps to NM_018323.3 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr4:71840891 G>T maps to ENST00000396051 G105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr4:71840891 G>T maps to ENST00000396051 G105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr4:84383770 G>T maps to NM_139076.2 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr4:84383770 G>T maps to NM_139076.2 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr4:187517873 C>A maps to ENST00000260147 E4277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr4:187517873 C>A maps to ENST00000260147 E4277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr5:1232406 C>T maps to NM_182632.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr5:1232406 C>T maps to NM_182632.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr5:52376452 T>C did not map to a codon.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr5:52376452 T>C did not map to a codon.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr6:24570135 G>A maps to NM_014809.3 H662H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr6:24570135 G>A maps to NM_014809.3 H662H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr6:31778360 C>G maps to NM_005527.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr6:31778360 C>G maps to NM_005527.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr6:35443390 G>A maps to ENST00000357281 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr6:35443390 G>A maps to ENST00000357281 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr6:84567049 C>G maps to NM_001009994.1 S110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr6:84567049 C>G maps to NM_001009994.1 S110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:6820508 C>A maps to NM_173565.3 C533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:6820508 C>A maps to NM_173565.3 C533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:20421483 C>T maps to NM_002214.2 N312N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:20421483 C>T maps to NM_002214.2 N312N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:21550739 G>A maps to NM_003112.3 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:21550739 G>A maps to NM_003112.3 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:21639715 C>T maps to NM_003777.3 H993H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:21639715 C>T maps to NM_003777.3 H993H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:38530745 C>G did not map to a codon.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:38530745 C>G did not map to a codon.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:72988771 G>T maps to NM_012453.2 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:72988771 G>T maps to NM_012453.2 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:73969807 G>A maps to NM_016328.2 K684K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:73969807 G>A maps to NM_016328.2 K684K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:100485055 G>A maps to NM_015908.5 V697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:100485055 G>A maps to NM_015908.5 V697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:142606702 G>A maps to NM_019841.4 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr7:142606702 G>A maps to NM_019841.4 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr9:130712746 C>T maps to NM_001035254.2 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr9:130712746 C>T maps to NM_001035254.2 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr9:139402770 G>A maps to NM_017617.3 Q1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr9:139402770 G>A maps to NM_017617.3 Q1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7391-01A-11D-2012-08 chr1:248844911 G>A maps to NM_001004734.1 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7391-01A-11D-2012-08 chr1:248844911 G>A maps to NM_001004734.1 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7391-01A-11D-2012-08 chr2:109352600 T>C maps to NM_006267.4 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7391-01A-11D-2012-08 chr2:109352600 T>C maps to NM_006267.4 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7391-01A-11D-2012-08 chr8:144946713 G>A maps to NM_031308.1 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7391-01A-11D-2012-08 chr8:144946713 G>A maps to NM_031308.1 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr1:113616159 C>G maps to NM_014813.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr1:113616159 C>G maps to NM_014813.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr1:244217658 C>T maps to NM_205768.2 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr1:244217658 C>T maps to NM_205768.2 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr19:40540671 T>A maps to NM_001005851.2 V698V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr19:40540671 T>A maps to NM_001005851.2 V698V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr3:112324347 G>A maps to ENST00000447230 Y934Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr3:112324347 G>A maps to ENST00000447230 Y934Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr5:41159280 G>A maps to NM_001115131.1 R587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr5:41159280 G>A maps to NM_001115131.1 R587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr6:26056368 C>G maps to NM_005319.3 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr6:26056368 C>G maps to NM_005319.3 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr6:31604565 G>A maps to NM_080686.2 P1997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr6:31604565 G>A maps to NM_080686.2 P1997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr7:891655 G>A maps to ENST00000456758 W465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr7:891655 G>A maps to ENST00000456758 W465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr7:1579887 C>T maps to NM_002360.3 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chr7:1579887 C>T maps to NM_002360.3 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chrX:69455617 G>A maps to NM_001013579.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7392-01A-11D-2012-08 chrX:69455617 G>A maps to NM_001013579.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7393-01A-11D-2012-08 chr17:55957075 A>G maps to NM_017949.1 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7393-01A-11D-2012-08 chr17:55957075 A>G maps to NM_017949.1 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr1:8425905 G>A maps to NM_012102.3 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr1:8425905 G>A maps to NM_012102.3 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr1:33832908 G>A maps to ENST00000419414 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr1:33832908 G>A maps to ENST00000419414 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr1:64643981 C>G maps to NM_005012.2 S753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr1:64643981 C>G maps to NM_005012.2 S753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr1:120548095 G>A maps to NM_024408.2 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr1:120548095 G>A maps to NM_024408.2 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr1:153964114 C>G maps to NM_001030.4 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr1:153964114 C>G maps to NM_001030.4 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr1:216680463 C>A maps to NM_001438.2 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr1:216680463 C>A maps to NM_001438.2 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr1:227300479 C>T maps to ENST00000366766 Q594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr1:227300479 C>T maps to ENST00000366766 Q594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr10:1061733 T>C maps to NM_012341.2 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr10:1061733 T>C maps to NM_012341.2 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr10:102039976 G>A maps to NM_173809.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr10:102039976 G>A maps to NM_173809.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr10:104157125 C>T maps to NM_001077494.1 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr10:104157125 C>T maps to NM_001077494.1 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr10:129839246 G>A maps to NM_006504.4 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr10:129839246 G>A maps to NM_006504.4 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr11:1862065 G>A maps to ENST00000381906 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr11:1862065 G>A maps to ENST00000381906 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr11:4967898 G>A maps to NM_001005329.1 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr11:4967898 G>A maps to NM_001005329.1 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr11:45950272 C>G maps to NM_152312.3 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr11:45950272 C>G maps to NM_152312.3 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr11:64012226 C>T maps to NM_138689.2 *148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr11:64012226 C>T maps to NM_138689.2 *148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr11:66358521 C>T maps to NM_018219.2 W655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr11:66358521 C>T maps to NM_018219.2 W655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr11:66407346 G>A maps to NM_002896.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr11:66407346 G>A maps to NM_002896.3 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr11:67050603 G>A maps to NM_001619.3 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr11:67050603 G>A maps to NM_001619.3 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr12:46245722 C>T maps to NM_152641.2 R1273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr12:46245722 C>T maps to NM_152641.2 R1273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr12:49580116 G>A maps to NM_006009.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr12:49580116 G>A maps to NM_006009.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr12:52913990 G>A maps to NM_000424.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr12:52913990 G>A maps to NM_000424.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr13:25914136 C>T maps to NM_014089.3 F555F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr13:25914136 C>T maps to NM_014089.3 F555F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr14:21825366 C>T maps to NM_007192.3 K883K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr14:21825366 C>T maps to NM_007192.3 K883K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr14:94750478 T>G maps to NM_001100607.1 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr14:94750478 T>G maps to NM_001100607.1 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr15:79092833 G>A maps to ENST00000258883 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr15:79092833 G>A maps to ENST00000258883 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr15:91172508 C>T maps to NM_022769.3 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr15:91172508 C>T maps to NM_022769.3 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr17:17120451 G>A maps to NM_144997.5 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr17:17120451 G>A maps to NM_144997.5 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr17:56320354 C>G maps to NM_006151.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr17:56320354 C>G maps to NM_006151.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr17:70120526 G>A maps to NM_000346.3 *510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr17:70120526 G>A maps to NM_000346.3 *510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr17:73729738 C>T maps to NM_001005619.1 F541F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr17:73729738 C>T maps to NM_001005619.1 F541F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr18:22805792 C>A maps to NM_015461.2 E697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr18:22805792 C>A maps to NM_015461.2 E697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr19:10394871 C>T maps to NM_000201.2 N267N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr19:10394871 C>T maps to NM_000201.2 N267N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr19:12384319 C>T maps to NM_001164276.1 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr19:12384319 C>T maps to NM_001164276.1 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr19:36113849 G>A maps to NM_015302.1 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr19:36113849 G>A maps to NM_015302.1 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr19:58773054 A>G maps to NM_014480.2 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr19:58773054 A>G maps to NM_014480.2 K361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr2:191524147 C>T maps to NM_005966.3 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr2:191524147 C>T maps to NM_005966.3 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr2:198299714 C>T maps to NM_012433.2 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr2:198299714 C>T maps to NM_012433.2 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr2:202137619 G>C did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr2:202137619 G>C did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr2:207530692 C>T maps to NM_001093730.1 Q347Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr2:207530692 C>T maps to NM_001093730.1 Q347Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr2:220355163 G>A maps to NM_005876.4 E2985E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr2:220355163 G>A maps to NM_005876.4 E2985E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr20:870885 C>T maps to NM_015985.2 Q145Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr20:870885 C>T maps to NM_015985.2 Q145Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr21:45821617 C>T maps to ENST00000397932 F792F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr21:45821617 C>T maps to ENST00000397932 F792F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr22:41574518 G>A maps to NM_001429.3 Q2268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr22:41574518 G>A maps to NM_001429.3 Q2268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr22:42461813 C>T maps to NM_000262.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr22:42461813 C>T maps to NM_000262.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr3:43381992 T>C did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr3:43381992 T>C did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr3:57875801 G>A maps to ENST00000428312 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr3:57875801 G>A maps to ENST00000428312 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr4:56830507 C>A maps to NM_025009.3 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr4:56830507 C>A maps to NM_025009.3 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr4:71509144 C>T maps to NM_031889.2 Q668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr4:71509144 C>T maps to NM_031889.2 Q668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr4:77057368 G>A maps to ENST00000458189 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr4:77057368 G>A maps to ENST00000458189 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr4:89618773 A>G maps to NM_153757.2 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr4:89618773 A>G maps to NM_153757.2 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr4:110791476 G>T maps to NM_198506.2 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr4:110791476 G>T maps to NM_198506.2 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr4:123159466 G>A maps to NM_015312.3 E1265E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr4:123159466 G>A maps to NM_015312.3 E1265E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr4:187535343 C>T did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr4:187535343 C>T did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr5:11346703 G>A maps to NM_001332.2 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr5:11346703 G>A maps to NM_001332.2 Q470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr5:66461495 G>A maps to NM_001164664.1 P2163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr5:66461495 G>A maps to NM_001164664.1 P2163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr5:96314944 T>C maps to NM_005575.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr5:96314944 T>C maps to NM_005575.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr5:96498920 C>T maps to NM_018343.2 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr5:96498920 C>T maps to NM_018343.2 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr5:137593488 G>A maps to NM_001496.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr5:137593488 G>A maps to NM_001496.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr5:176310831 C>T maps to NM_002115.2 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr5:176310831 C>T maps to NM_002115.2 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr6:26093371 C>T maps to NM_000410.3 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr6:26093371 C>T maps to NM_000410.3 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr6:132201069 C>T maps to NM_006208.2 Q666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr6:132201069 C>T maps to NM_006208.2 Q666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr7:15725556 C>T maps to NM_005924.4 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr7:15725556 C>T maps to NM_005924.4 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr7:64168430 A>G maps to NM_016220.3 E583E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr7:64168430 A>G maps to NM_016220.3 E583E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr7:99701069 G>A maps to ENST00000429084 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr7:99701069 G>A maps to ENST00000429084 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr7:128356920 C>T maps to NM_032599.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr7:128356920 C>T maps to NM_032599.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr7:131913118 G>A maps to NM_020911.1 Q572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr7:131913118 G>A maps to NM_020911.1 Q572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr7:138455986 C>T maps to NM_130840.2 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr7:138455986 C>T maps to NM_130840.2 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr7:148487476 C>T maps to NM_003592.2 Q584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr7:148487476 C>T maps to NM_003592.2 Q584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr8:12878805 G>A maps to NM_020844.2 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr8:12878805 G>A maps to NM_020844.2 Q206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr9:21971027 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr9:21971027 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr9:95013062 C>T maps to ENST00000375660 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr9:95013062 C>T maps to ENST00000375660 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr9:98268845 C>G maps to NM_000264.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr9:98268845 C>G maps to NM_000264.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr9:139395017 G>A maps to NM_017617.3 Q1974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr9:139395017 G>A maps to NM_017617.3 Q1974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr9:140946542 G>A did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chr9:140946542 G>A did not map to a codon.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chrX:108926544 A>G maps to NM_022977.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chrX:108926544 A>G maps to NM_022977.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chrX:118220734 C>T maps to NM_020721.1 S1486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chrX:118220734 C>T maps to NM_020721.1 S1486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chrX:152960238 G>A maps to NM_005629.3 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7394-01A-11D-2012-08 chrX:152960238 G>A maps to NM_005629.3 P554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr1:36785433 C>T maps to NM_001162530.1 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr1:36785433 C>T maps to NM_001162530.1 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr1:53580587 G>A maps to NM_006671.4 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr1:53580587 G>A maps to NM_006671.4 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr1:84864282 A>T maps to NM_021233.2 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr1:84864282 A>T maps to NM_021233.2 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr1:186026438 G>A maps to NM_031935.2 L2406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr1:186026438 G>A maps to NM_031935.2 L2406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr1:204943328 G>A maps to ENST00000367172 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr1:204943328 G>A maps to ENST00000367172 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr1:247921357 C>A maps to NM_012353.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr1:247921357 C>A maps to NM_012353.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr10:97917734 T>C maps to NM_014803.3 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr10:97917734 T>C maps to NM_014803.3 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr10:105205278 G>A maps to NM_014976.1 E1863E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr10:105205278 G>A maps to NM_014976.1 E1863E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr12:46233279 G>A did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr12:46233279 G>A did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr12:51584077 G>A maps to NM_002702.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr12:51584077 G>A maps to NM_002702.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr12:75601706 G>A maps to NM_139137.2 H19H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr12:75601706 G>A maps to NM_139137.2 H19H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr12:103288645 C>T maps to NM_000277.1 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr12:103288645 C>T maps to NM_000277.1 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr13:39264177 A>G maps to NM_207361.4 R899R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr13:39264177 A>G maps to NM_207361.4 R899R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr14:20529069 G>A maps to NM_001004717.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr14:20529069 G>A maps to NM_001004717.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr14:105916416 G>A maps to NM_004689.3 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr14:105916416 G>A maps to NM_004689.3 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr15:26806249 G>C maps to NM_021912.4 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr15:26806249 G>C maps to NM_021912.4 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr15:40630981 C>T maps to NM_207380.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr15:40630981 C>T maps to NM_207380.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr15:85201311 G>A maps to NM_205858.1 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr15:85201311 G>A maps to NM_205858.1 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr15:91448551 C>T maps to NM_006122.2 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr15:91448551 C>T maps to NM_006122.2 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr16:15501679 G>A did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr16:15501679 G>A did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr16:22320754 G>A maps to NM_018119.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr16:22320754 G>A maps to NM_018119.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr16:22926537 C>G maps to NM_006043.1 Y253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr16:22926537 C>G maps to NM_006043.1 Y253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr16:30723671 G>A maps to NM_006662.2 K635K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr16:30723671 G>A maps to NM_006662.2 K635K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr16:71683623 G>A maps to NM_015020.2 L1047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr16:71683623 G>A maps to NM_015020.2 L1047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr16:72137933 C>T maps to NM_014003.3 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr16:72137933 C>T maps to NM_014003.3 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr16:81929466 G>A maps to NM_002661.2 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr16:81929466 G>A maps to NM_002661.2 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr17:3724645 C>T maps to NM_001114118.1 W299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr17:3724645 C>T maps to NM_001114118.1 W299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr17:7695574 G>A maps to NM_020877.2 T2353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr17:7695574 G>A maps to NM_020877.2 T2353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr17:16005051 G>A maps to ENST00000395857 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr17:16005051 G>A maps to ENST00000395857 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr17:26961607 A>G maps to NM_014680.2 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr17:26961607 A>G maps to NM_014680.2 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr17:55183031 C>T maps to ENST00000427138 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr17:55183031 C>T maps to ENST00000427138 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr17:63533162 G>A maps to NM_004655.3 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr17:63533162 G>A maps to NM_004655.3 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr17:79226903 C>T maps to NM_001037984.1 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr17:79226903 C>T maps to NM_001037984.1 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr18:580650 G>T maps to NM_004066.1 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr18:580650 G>T maps to NM_004066.1 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr18:59221474 C>A maps to NM_031891.2 I651I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr18:59221474 C>A maps to NM_031891.2 I651I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr19:2121735 C>T maps to ENST00000355272 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr19:2121735 C>T maps to ENST00000355272 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr19:11943308 C>T maps to NM_152357.2 Q440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr19:11943308 C>T maps to NM_152357.2 Q440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr19:14161618 C>A maps to NM_004843.2 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr19:14161618 C>A maps to NM_004843.2 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr19:52001377 C>A maps to NM_053003.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr19:52001377 C>A maps to NM_053003.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr2:30961323 C>T did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr2:30961323 C>T did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr2:107032305 C>T maps to ENST00000304514 K1688K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr2:107032305 C>T maps to ENST00000304514 K1688K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr2:121748214 C>T maps to NM_005270.4 L1575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr2:121748214 C>T maps to NM_005270.4 L1575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr2:179481234 G>A maps to NM_133378.4 R13527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr2:179481234 G>A maps to NM_133378.4 R13527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr20:13280033 C>T maps to NM_080826.1 N441N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr20:13280033 C>T maps to NM_080826.1 N441N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr22:41572249 G>A did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr22:41572249 G>A did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr22:44340651 G>A maps to NM_025225.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr22:44340651 G>A maps to NM_025225.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr3:39230362 T>G maps to NM_194293.2 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr3:39230362 T>G maps to NM_194293.2 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr3:39307505 G>A maps to NM_001171174.1 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr3:39307505 G>A maps to NM_001171174.1 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr3:44609917 C>T maps to NM_018651.2 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr3:44609917 C>T maps to NM_018651.2 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr3:44609920 C>T maps to NM_018651.2 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr3:44609920 C>T maps to NM_018651.2 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr3:97887665 G>C maps to NM_001005515.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr3:97887665 G>C maps to NM_001005515.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr3:137483940 C>G maps to NM_004189.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr3:137483940 C>G maps to NM_004189.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr4:156618129 A>G maps to NM_001130684.1 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr4:156618129 A>G maps to NM_001130684.1 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr4:187628808 G>A maps to ENST00000260147 Q725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr4:187628808 G>A maps to ENST00000260147 Q725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr5:35037139 G>A maps to NM_031900.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr5:35037139 G>A maps to NM_031900.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr5:37327822 A>C maps to NM_153485.1 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr5:37327822 A>C maps to NM_153485.1 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr5:37605303 G>A maps to NM_018034.2 Q352Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr5:37605303 G>A maps to NM_018034.2 Q352Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr5:145895391 T>C maps to NM_194251.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr5:145895391 T>C maps to NM_194251.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:17551729 G>A maps to NM_006366.2 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:17551729 G>A maps to NM_006366.2 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:18121916 C>T maps to NM_198586.2 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:18121916 C>T maps to NM_198586.2 V307V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CR-7395-01A-11D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:24357945 C>T maps to NM_181337.3 Q27*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CR-7395-01A-11D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:24357945 C>T maps to NM_181337.3 Q27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:29910404 T>G did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:29910404 T>G did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:32138237 G>A maps to NM_032741.4 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:32138237 G>A maps to NM_032741.4 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:33679328 G>A maps to NM_032340.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:33679328 G>A maps to NM_032340.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:79668288 G>A maps to NM_017934.5 R1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:79668288 G>A maps to NM_017934.5 R1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:83841950 G>A maps to NM_015018.2 Q891Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr6:83841950 G>A maps to NM_015018.2 Q891Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr7:99794805 C>T maps to NM_012447.2 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr7:99794805 C>T maps to NM_012447.2 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr7:132192786 G>A maps to NM_020911.1 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr7:132192786 G>A maps to NM_020911.1 F222F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr7:138602130 A>G maps to NM_001164665.1 A747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr7:138602130 A>G maps to NM_001164665.1 A747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr8:6566209 C>G maps to NM_018361.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr8:6566209 C>G maps to NM_018361.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr8:27995258 C>T maps to NM_018091.5 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr8:27995258 C>T maps to NM_018091.5 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr9:124751884 G>A maps to NM_001139442.1 C376C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr9:124751884 G>A maps to NM_001139442.1 C376C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr9:131864309 A>G maps to NM_000755.3 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr9:131864309 A>G maps to NM_000755.3 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chrX:41048593 C>T maps to NM_001039590.2 D1281D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chrX:41048593 C>T maps to NM_001039590.2 D1281D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chrX:123159746 C>T maps to NM_001042750.1 N34N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chrX:123159746 C>T maps to NM_001042750.1 N34N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chrX:153696644 G>A did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chrX:153696644 G>A did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chrX:154128149 A>C maps to NM_000132.3 S2088S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chrX:154128149 A>C maps to NM_000132.3 S2088S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr1:67195003 A>G maps to ENST00000237247 R631R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr1:67195003 A>G maps to ENST00000237247 R631R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr1:144618123 G>T maps to NM_001037675.2 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr1:144618123 G>T maps to NM_001037675.2 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr1:244218371 C>T maps to NM_205768.2 Y432Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr1:244218371 C>T maps to NM_205768.2 Y432Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr1:248263540 C>A maps to NM_175911.2 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr1:248263540 C>A maps to NM_175911.2 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr12:56575489 C>A maps to NM_003075.3 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr12:56575489 C>A maps to NM_003075.3 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr15:28538127 C>T maps to NM_004667.4 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr15:28538127 C>T maps to NM_004667.4 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr17:3470182 G>A maps to ENST00000399756 R827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr17:3470182 G>A maps to ENST00000399756 R827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr17:21319865 C>T maps to NM_021012.4 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr17:21319865 C>T maps to NM_021012.4 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr17:38142871 A>G maps to NM_002809.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr17:38142871 A>G maps to NM_002809.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr19:23836192 G>A maps to NM_138330.2 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr19:23836192 G>A maps to NM_138330.2 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr19:39361609 G>A maps to NM_001195833.1 H208H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr19:39361609 G>A maps to NM_001195833.1 H208H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr2:220144590 A>T maps to NM_006736.5 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr2:220144590 A>T maps to NM_006736.5 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr3:127983608 G>A maps to NM_021937.3 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr3:127983608 G>A maps to NM_021937.3 E257E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr4:44450255 C>T maps to NM_198353.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr4:44450255 C>T maps to NM_198353.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr5:137727715 C>T maps to NM_016604.3 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr5:137727715 C>T maps to NM_016604.3 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr5:176018403 G>A did not map to a codon.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr5:176018403 G>A did not map to a codon.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr6:31736951 G>C maps to NM_025258.2 S449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr6:31736951 G>C maps to NM_025258.2 S449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr7:70236611 A>G maps to NM_015570.2 Q604Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr7:70236611 A>G maps to NM_015570.2 Q604Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr9:98220447 C>A maps to NM_000264.3 G1005G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chr9:98220447 C>A maps to NM_000264.3 G1005G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chrX:63444271 G>A maps to NM_130388.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chrX:63444271 G>A maps to NM_130388.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chrX:119077226 C>T maps to NM_024528.3 W114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7397-01A-11D-2012-08 chrX:119077226 C>T maps to NM_024528.3 W114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:34329944 C>A maps to NM_145205.4 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:34329944 C>A maps to NM_145205.4 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:45506090 G>A maps to NM_020883.1 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:45506090 G>A maps to NM_020883.1 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:68512914 G>A maps to NM_004675.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:68512914 G>A maps to NM_004675.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:79403498 C>A maps to NM_022159.3 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:79403498 C>A maps to NM_022159.3 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:103440440 T>A did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:103440440 T>A did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:152659535 C>T maps to NM_014357.4 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:152659535 C>T maps to NM_014357.4 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:158669656 G>A maps to NM_001005279.1 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:158669656 G>A maps to NM_001005279.1 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:166927158 G>T maps to NM_199351.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:166927158 G>T maps to NM_199351.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:231047214 C>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:231047214 C>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:237942009 G>T maps to NM_001035.2 L3940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:237942009 G>T maps to NM_001035.2 L3940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:247599292 A>G maps to NM_004895.4 T840T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:247599292 A>G maps to NM_004895.4 T840T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:248512789 C>G maps to NM_001001918.1 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr1:248512789 C>G maps to NM_001001918.1 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr10:93791 C>A maps to NM_177987.2 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr10:93791 C>A maps to NM_177987.2 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr10:17165685 A>T maps to NM_001081.3 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr10:17165685 A>T maps to NM_001081.3 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr10:100481442 C>A maps to NM_021828.4 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr10:100481442 C>A maps to NM_021828.4 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr10:135106019 G>A maps to NM_006659.2 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr10:135106019 G>A maps to NM_006659.2 I399I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:5730670 G>A maps to NM_006074.4 K430K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:5730670 G>A maps to NM_006074.4 K430K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:7068025 G>T maps to NM_176822.3 E696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:7068025 G>T maps to NM_176822.3 E696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:55927361 C>G maps to NM_001004058.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:55927361 C>G maps to NM_001004058.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:59622198 A>G maps to NM_001062.3 N349N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:59622198 A>G maps to NM_001062.3 N349N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:76870541 G>C maps to NM_000260.3 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:76870541 G>C maps to NM_000260.3 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:105795454 C>T maps to NM_000829.3 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:105795454 C>T maps to NM_000829.3 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:114027107 C>A maps to NM_001018011.1 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:114027107 C>A maps to NM_001018011.1 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:124413187 G>C maps to NM_001005195.1 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:124413187 G>C maps to NM_001005195.1 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:126343308 C>T maps to NM_032531.3 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:126343308 C>T maps to NM_032531.3 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:128360448 T>A maps to NM_001143820.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr11:128360448 T>A maps to NM_001143820.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr12:11546828 G>T maps to NM_006248.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr12:11546828 G>T maps to NM_006248.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr12:13224191 T>A maps to NM_020853.1 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr12:13224191 T>A maps to NM_020853.1 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr12:26580956 C>A maps to NM_002223.2 L2278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr12:26580956 C>A maps to NM_002223.2 L2278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr12:60168918 G>T maps to NM_004731.3 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr12:60168918 G>T maps to NM_004731.3 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr12:64472739 T>C maps to NM_020762.2 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr12:64472739 T>C maps to NM_020762.2 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr13:48881511 G>A maps to NM_000321.2 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr13:48881511 G>A maps to NM_000321.2 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr13:49957000 C>A maps to NM_001079670.1 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr13:49957000 C>A maps to NM_001079670.1 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr14:20389062 C>T maps to NM_001005483.1 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr14:20389062 C>T maps to NM_001005483.1 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr14:24785366 G>T maps to NM_181657.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr14:24785366 G>T maps to NM_181657.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr14:74060509 C>T maps to NM_152331.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr14:74060509 C>T maps to NM_152331.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr15:40494808 C>T maps to ENST00000412359 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr15:40494808 C>T maps to ENST00000412359 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr15:54586183 G>T maps to ENST00000260323 E1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr15:54586183 G>T maps to ENST00000260323 E1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr15:87066039 G>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr15:87066039 G>T did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr16:9857767 G>A maps to NM_000833.3 S1211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr16:9857767 G>A maps to NM_000833.3 S1211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr16:30749356 G>T maps to NM_006662.2 E2666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr16:30749356 G>T maps to NM_006662.2 E2666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr17:8044496 G>A maps to NM_002616.2 A1254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr17:8044496 G>A maps to NM_002616.2 A1254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr17:49074018 C>T maps to ENST00000376407 K625K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr17:49074018 C>T maps to ENST00000376407 K625K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr17:72348367 G>T maps to NM_153209.3 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr17:72348367 G>T maps to NM_153209.3 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr18:3129466 C>A maps to NM_003803.3 G853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr18:3129466 C>A maps to NM_003803.3 G853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr18:13681842 T>A maps to NM_152352.3 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr18:13681842 T>A maps to NM_152352.3 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr18:43795986 G>T maps to NM_145055.3 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr18:43795986 G>T maps to NM_145055.3 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr18:44560255 T>C maps to NM_016427.2 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr18:44560255 T>C maps to NM_016427.2 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:813187 G>A maps to NM_024888.1 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:813187 G>A maps to NM_024888.1 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:10265724 G>A maps to NM_001130823.1 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:10265724 G>A maps to NM_001130823.1 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:12958434 C>T maps to NM_014975.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:12958434 C>T maps to NM_014975.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:14163008 C>A maps to NM_004843.2 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:14163008 C>A maps to NM_004843.2 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:16275695 C>A maps to NM_054113.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:16275695 C>A maps to NM_054113.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:33333130 C>A maps to NM_014270.4 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:33333130 C>A maps to NM_014270.4 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:50245222 C>T maps to NM_021733.1 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:50245222 C>T maps to NM_021733.1 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:51503432 G>A maps to NM_144505.1 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr19:51503432 G>A maps to NM_144505.1 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:26852279 G>T maps to NM_001029881.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:26852279 G>T maps to NM_001029881.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:48873733 A>G maps to NM_172311.2 P881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:48873733 A>G maps to NM_172311.2 P881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:105858977 G>A maps to NM_007227.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:105858977 G>A maps to NM_007227.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:163292053 G>T maps to NM_033272.2 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:163292053 G>T maps to NM_033272.2 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:170058312 G>T maps to NM_004525.2 R2759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:170058312 G>T maps to NM_004525.2 R2759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:182783379 C>G maps to NM_001130445.1 S948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:182783379 C>G maps to NM_001130445.1 S948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:189909939 C>A maps to NM_000393.3 G1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:189909939 C>A maps to NM_000393.3 G1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:237489773 C>T maps to NM_020311.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:237489773 C>T maps to NM_020311.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:238449172 G>T maps to NM_024101.5 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:238449172 G>T maps to NM_024101.5 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:239344390 C>T maps to NM_001040445.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:239344390 C>T maps to NM_001040445.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:240029766 C>T maps to NM_006037.3 T692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:240029766 C>T maps to NM_006037.3 T692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:241534550 C>A maps to NM_023083.3 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr2:241534550 C>A maps to NM_023083.3 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr20:2577847 C>T maps to NM_080751.2 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr20:2577847 C>T maps to NM_080751.2 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr20:3210333 G>A maps to NM_001174090.1 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr20:3210333 G>A maps to NM_001174090.1 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr21:10910381 T>C maps to NM_199261.2 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr21:10910381 T>C maps to NM_199261.2 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr21:10969097 G>T maps to NM_199261.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr21:10969097 G>T maps to NM_199261.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr21:45978295 C>T maps to NM_198696.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr21:45978295 C>T maps to NM_198696.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr21:46912602 C>A maps to ENST00000359759 G1145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr21:46912602 C>A maps to ENST00000359759 G1145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr22:39910114 C>T maps to NM_019008.4 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr22:39910114 C>T maps to NM_019008.4 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr3:39229739 C>A maps to NM_194293.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr3:39229739 C>A maps to NM_194293.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr3:157146251 T>C maps to NM_001167912.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr3:157146251 T>C maps to NM_001167912.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr3:164704992 G>A maps to NM_001041.3 L1710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr3:164704992 G>A maps to NM_001041.3 L1710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr3:164741484 G>T maps to NM_001041.3 S991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr3:164741484 G>T maps to NM_001041.3 S991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr3:186450366 G>T maps to NM_001102416.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr3:186450366 G>T maps to NM_001102416.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr4:5458559 G>A maps to NM_018401.1 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr4:5458559 G>A maps to NM_018401.1 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr4:71068635 T>C did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr4:71068635 T>C did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr4:162841697 A>T maps to NM_020116.3 C89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr4:162841697 A>T maps to NM_020116.3 C89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr5:33937867 C>A maps to NM_016568.3 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr5:33937867 C>A maps to NM_016568.3 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr5:35727887 C>A maps to NM_024867.3 S1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr5:35727887 C>A maps to NM_024867.3 S1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr5:41939627 A>G maps to NM_012176.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr5:41939627 A>G maps to NM_012176.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr5:79498803 G>C maps to NM_001174072.1 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr5:79498803 G>C maps to NM_001174072.1 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr5:112175214 A>G maps to NM_001127510.2 K1308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr5:112175214 A>G maps to NM_001127510.2 K1308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr5:140176492 C>T maps to NM_018905.2 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr5:140176492 C>T maps to NM_018905.2 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr5:169461489 G>A maps to NM_004946.2 L1185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr5:169461489 G>A maps to NM_004946.2 L1185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:29274873 C>G maps to NM_030946.1 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:29274873 C>G maps to NM_030946.1 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:29408337 T>A maps to NM_013941.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:29408337 T>A maps to NM_013941.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:30297213 C>T maps to NM_021253.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:30297213 C>T maps to NM_021253.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:31743182 C>T maps to NM_025258.2 W179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:31743182 C>T maps to NM_025258.2 W179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:44219989 A>T maps to NM_007355.2 K573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:44219989 A>T maps to NM_007355.2 K573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:46108937 C>T maps to NM_014936.4 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:46108937 C>T maps to NM_014936.4 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:51484070 C>T maps to NM_138694.3 L4011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:51484070 C>T maps to NM_138694.3 L4011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:88127993 C>A maps to NM_001031743.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:88127993 C>A maps to NM_001031743.2 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:136597401 T>A maps to NM_014739.2 K421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:136597401 T>A maps to NM_014739.2 K421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:144507959 G>T maps to NM_003764.3 G66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:144507959 G>T maps to NM_003764.3 G66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:146720538 G>C maps to NM_000838.3 A788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:146720538 G>C maps to NM_000838.3 A788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:159677660 G>T maps to NM_032532.2 T1724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr6:159677660 G>T maps to NM_032532.2 T1724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr7:53103796 G>T maps to NM_182595.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr7:53103796 G>T maps to NM_182595.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr8:37623866 T>C maps to NM_007198.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr8:37623866 T>C maps to NM_007198.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr8:48697682 C>A maps to NM_006904.6 E3699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr8:48697682 C>A maps to NM_006904.6 E3699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr8:93003885 C>T maps to NM_175634.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr8:93003885 C>T maps to NM_175634.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr8:103297761 G>C maps to NM_015902.4 Y1821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr8:103297761 G>C maps to NM_015902.4 Y1821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr8:113259247 C>A did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr8:113259247 C>A did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr8:120430511 A>T maps to NM_002514.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr8:120430511 A>T maps to NM_002514.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr8:143832541 C>A maps to NM_205545.1 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr8:143832541 C>A maps to NM_205545.1 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr9:98678716 G>A did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr9:98678716 G>A did not map to a codon.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr9:116764923 G>T maps to ENST00000374126 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr9:116764923 G>T maps to ENST00000374126 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr9:117071685 C>T maps to NM_032888.2 F1788F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr9:117071685 C>T maps to NM_032888.2 F1788F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr9:123550176 C>T maps to NM_012164.3 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr9:123550176 C>T maps to NM_012164.3 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr9:125391640 G>A maps to NM_001004450.1 H58H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr9:125391640 G>A maps to NM_001004450.1 H58H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr9:140901298 G>A maps to ENST00000277549 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chr9:140901298 G>A maps to ENST00000277549 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chrX:21674748 G>A maps to NM_153270.1 D386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chrX:21674748 G>A maps to NM_153270.1 D386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chrX:32361264 C>A maps to ENST00000357033 E1909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chrX:32361264 C>A maps to ENST00000357033 E1909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chrX:73963236 G>T maps to NM_001008537.2 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chrX:73963236 G>T maps to NM_001008537.2 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chrX:77392459 G>T maps to NM_015975.4 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chrX:77392459 G>T maps to NM_015975.4 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chrX:104464079 C>T maps to NM_031274.3 E266E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chrX:104464079 C>T maps to NM_031274.3 E266E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chrX:107977345 G>C maps to NM_003604.2 Y743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chrX:107977345 G>C maps to NM_003604.2 Y743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chrX:140996135 C>A maps to NM_005462.4 L982L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chrX:140996135 C>A maps to NM_005462.4 L982L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chrX:150780161 G>C maps to NM_173493.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chrX:150780161 G>C maps to NM_173493.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chrX:150791485 C>A maps to NM_173493.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chrX:150791485 C>A maps to NM_173493.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chrX:150840133 G>T maps to NM_173493.2 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7398-01A-11D-2012-08 chrX:150840133 G>T maps to NM_173493.2 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:94997875 C>T did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:94997875 C>T did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:94997898 G>T maps to NM_001993.4 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:94997898 G>T maps to NM_001993.4 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:152882572 A>G maps to NM_005547.2 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:152882572 A>G maps to NM_005547.2 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:156882414 G>T did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:156882414 G>T did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:158641850 C>A maps to NM_003126.2 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:158641850 C>A maps to NM_003126.2 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:165532976 C>T maps to NM_001005214.3 D286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:165532976 C>T maps to NM_001005214.3 D286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:169565301 G>T maps to NM_003005.3 Y654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:169565301 G>T maps to NM_003005.3 Y654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:213134596 G>T did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:213134596 G>T did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:214488114 G>A maps to NM_020197.2 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:214488114 G>A maps to NM_020197.2 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:222721185 G>A maps to NM_024746.3 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:222721185 G>A maps to NM_024746.3 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:229773041 C>T maps to NM_014777.2 I894I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:229773041 C>T maps to NM_014777.2 I894I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:236729216 A>T did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:236729216 A>T did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:243349133 C>A maps to NM_014812.2 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:243349133 C>A maps to NM_014812.2 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:247599409 C>A maps to NM_004895.4 A879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr1:247599409 C>A maps to NM_004895.4 A879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr10:54529050 G>C maps to NM_000242.2 S110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr10:54529050 G>C maps to NM_000242.2 S110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr10:63957981 G>A maps to NM_145307.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr10:63957981 G>A maps to NM_145307.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr10:67726464 G>A maps to NM_013266.2 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr10:67726464 G>A maps to NM_013266.2 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr10:75560117 C>G maps to NM_015037.2 T1638T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr10:75560117 C>G maps to NM_015037.2 T1638T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr10:85992039 G>T maps to NM_015613.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr10:85992039 G>T maps to NM_015613.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr10:96064339 C>T maps to ENST00000371380 Q1854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr10:96064339 C>T maps to ENST00000371380 Q1854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr10:135440299 G>C did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr10:135440299 G>C did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr11:4945220 G>A maps to NM_001005237.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr11:4945220 G>A maps to NM_001005237.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr11:5809560 A>C maps to NM_001001913.1 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr11:5809560 A>C maps to NM_001001913.1 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr11:22396419 C>A maps to NM_020346.2 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr11:22396419 C>A maps to NM_020346.2 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr11:51411501 G>C maps to NM_001005272.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr11:51411501 G>C maps to NM_001005272.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr11:55579652 C>T maps to NM_001004738.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr11:55579652 C>T maps to NM_001004738.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr11:123480965 C>T maps to ENST00000456860 H477H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr11:123480965 C>T maps to ENST00000456860 H477H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr11:124266425 A>T maps to NM_001005467.1 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr11:124266425 A>T maps to NM_001005467.1 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr12:2690863 G>T maps to NM_199460.2 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr12:2690863 G>T maps to NM_199460.2 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr12:20968718 C>G maps to NM_019844.2 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr12:20968718 C>G maps to NM_019844.2 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr13:21751048 A>C did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr13:21751048 A>C did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr13:32313844 T>C did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr13:32313844 T>C did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr13:86369425 C>T maps to NM_032229.2 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr13:86369425 C>T maps to NM_032229.2 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr14:29237168 C>A maps to NM_005249.3 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr14:29237168 C>A maps to NM_005249.3 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr15:23811611 C>A maps to NM_005664.3 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr15:23811611 C>A maps to NM_005664.3 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr16:30518143 G>A maps to NM_002209.2 P825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr16:30518143 G>A maps to NM_002209.2 P825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr16:46771726 C>T maps to NM_182493.2 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr16:46771726 C>T maps to NM_182493.2 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr17:7851509 C>T maps to NM_001037144.4 Q749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr17:7851509 C>T maps to NM_001037144.4 Q749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr17:10318850 G>A maps to NM_002472.2 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr17:10318850 G>A maps to NM_002472.2 Q196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr17:16203243 C>T maps to NM_004278.3 H126H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr17:16203243 C>T maps to NM_004278.3 H126H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr17:26942795 G>A maps to NM_014680.2 D2137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr17:26942795 G>A maps to NM_014680.2 D2137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr17:46673847 C>T maps to NM_018952.4 W201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr17:46673847 C>T maps to NM_018952.4 W201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr17:76967753 C>T maps to NM_005567.3 K554K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr17:76967753 C>T maps to NM_005567.3 K554K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr19:5783813 C>A maps to NM_001134316.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr19:5783813 C>A maps to NM_001134316.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr19:9012851 G>T maps to NM_024690.2 T12864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr19:9012851 G>T maps to NM_024690.2 T12864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr19:17122306 G>A maps to ENST00000443236 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr19:17122306 G>A maps to ENST00000443236 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr19:47259843 G>C maps to NM_024301.4 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr19:47259843 G>C maps to NM_024301.4 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr19:57326338 G>T maps to NM_006210.2 Y1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr19:57326338 G>T maps to NM_006210.2 Y1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr2:68613640 C>T maps to NM_002664.2 C160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr2:68613640 C>T maps to NM_002664.2 C160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr2:74043890 C>A maps to NM_001080474.1 I847I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr2:74043890 C>A maps to NM_001080474.1 I847I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr2:103324785 G>C maps to NM_003048.3 T759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr2:103324785 G>C maps to NM_003048.3 T759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr2:109405344 A>T maps to NM_144978.1 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr2:109405344 A>T maps to NM_144978.1 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr2:116497459 G>T maps to NM_020868.3 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr2:116497459 G>T maps to NM_020868.3 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr2:155555718 C>A maps to NM_002239.2 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr2:155555718 C>A maps to NM_002239.2 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr3:1269677 G>T did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr3:1269677 G>T did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr3:36570190 A>T maps to NM_003149.1 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr3:36570190 A>T maps to NM_003149.1 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr3:85932570 C>G maps to NM_153184.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr3:85932570 C>G maps to NM_153184.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr3:97806801 G>T maps to NM_054106.1 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr3:97806801 G>T maps to NM_054106.1 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr3:113172676 G>C maps to NM_144718.3 S593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr3:113172676 G>C maps to NM_144718.3 S593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr3:138669185 C>A maps to NM_001040061.2 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr3:138669185 C>A maps to NM_001040061.2 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr3:143691743 C>T maps to NM_173552.3 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr3:143691743 C>T maps to NM_173552.3 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr4:47857089 T>A maps to NM_152995.4 K803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr4:47857089 T>A maps to NM_152995.4 K803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr4:165118529 T>A maps to NM_012403.1 K112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr4:165118529 T>A maps to NM_012403.1 K112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr5:38427225 G>T maps to ENST00000354891 R642R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr5:38427225 G>T maps to ENST00000354891 R642R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr5:38427333 C>T maps to ENST00000354891 G678G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr5:38427333 C>T maps to ENST00000354891 G678G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr5:140530920 C>A maps to NM_018939.2 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr5:140530920 C>A maps to NM_018939.2 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr5:140558045 C>G maps to NM_019120.2 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr5:140558045 C>G maps to NM_019120.2 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr5:169468121 G>C maps to NM_004946.2 T1243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr5:169468121 G>C maps to NM_004946.2 T1243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr5:179666939 T>C maps to NM_002752.4 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr5:179666939 T>C maps to NM_002752.4 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr5:180043407 G>T maps to NM_182925.4 R1060R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr5:180043407 G>T maps to NM_182925.4 R1060R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr6:20102579 T>C maps to NM_001080480.1 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr6:20102579 T>C maps to NM_001080480.1 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr6:43749749 G>A maps to NM_001025366.2 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr6:43749749 G>A maps to NM_001025366.2 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr6:118015290 G>A maps to NM_138459.3 Q213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr6:118015290 G>A maps to NM_138459.3 Q213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr6:121526219 C>T did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr6:121526219 C>T did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr7:30706891 C>T maps to ENST00000348438 W116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr7:30706891 C>T maps to ENST00000348438 W116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr7:86569410 T>G maps to NM_001142749.2 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr7:86569410 T>G maps to NM_001142749.2 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr7:99565929 C>T maps to NM_001185.3 W154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr7:99565929 C>T maps to NM_001185.3 W154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr7:149481148 C>G maps to NM_198455.2 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr7:149481148 C>G maps to NM_198455.2 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr7:154875974 C>G maps to NM_024012.2 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr7:154875974 C>G maps to NM_024012.2 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:1497071 G>T maps to ENST00000357934 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:1497071 G>T maps to ENST00000357934 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:6378819 G>A maps to NM_001147.2 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:6378819 G>A maps to NM_001147.2 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:21957262 G>C maps to NM_022749.5 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:21957262 G>C maps to NM_022749.5 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:24358342 C>T maps to ENST00000380789 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:24358342 C>T maps to ENST00000380789 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:68044263 G>A maps to ENST00000389042 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:68044263 G>A maps to ENST00000389042 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:72211955 C>A did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:72211955 C>A did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:113243842 C>A maps to NM_198123.1 G3587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:113243842 C>A maps to NM_198123.1 G3587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:133142132 C>A maps to NM_004519.2 S665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:133142132 C>A maps to NM_004519.2 S665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:139323162 C>T maps to NM_015912.3 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:139323162 C>T maps to NM_015912.3 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:143994780 G>T maps to NM_000498.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr8:143994780 G>T maps to NM_000498.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr9:37860054 A>G maps to NM_024345.3 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr9:37860054 A>G maps to NM_024345.3 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr9:73151900 T>A maps to ENST00000419692 L1330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr9:73151900 T>A maps to ENST00000419692 L1330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr9:118973929 T>A maps to NM_002581.3 L546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr9:118973929 T>A maps to NM_002581.3 L546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chrX:30269596 C>A maps to NM_177404.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chrX:30269596 C>A maps to NM_177404.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chrX:38145137 T>C maps to NM_001034853.1 E1038E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chrX:38145137 T>C maps to NM_001034853.1 E1038E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chrX:77393353 T>C maps to NM_015975.4 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chrX:77393353 T>C maps to NM_015975.4 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chrX:85969659 C>A maps to NM_053281.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chrX:85969659 C>A maps to NM_053281.3 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chrX:110644216 C>A did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chrX:110644216 C>A did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chrX:114540769 G>T maps to NM_016383.3 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chrX:114540769 G>T maps to NM_016383.3 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr1:35484993 G>A maps to NM_007167.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr1:35484993 G>A maps to NM_007167.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr1:200550380 G>A maps to NM_014875.2 Q1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr1:200550380 G>A maps to NM_014875.2 Q1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr1:235940476 G>A maps to NM_000081.2 S1782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr1:235940476 G>A maps to NM_000081.2 S1782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr11:17126755 C>T maps to NM_002645.2 W1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr11:17126755 C>T maps to NM_002645.2 W1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr11:106810419 A>G maps to ENST00000282249 C324C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr11:106810419 A>G maps to ENST00000282249 C324C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr11:132527153 G>A maps to NM_002545.3 Y76Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr11:132527153 G>A maps to NM_002545.3 Y76Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr12:19413941 C>G maps to ENST00000429027 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr12:19413941 C>G maps to ENST00000429027 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr13:29252223 A>G maps to NM_015932.5 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr13:29252223 A>G maps to NM_015932.5 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr13:38211558 C>T maps to NM_003306.1 P810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr13:38211558 C>T maps to NM_003306.1 P810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr14:75376270 G>A maps to NM_031464.3 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr14:75376270 G>A maps to NM_031464.3 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr14:94120289 G>C maps to ENST00000393153 G2128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr14:94120289 G>C maps to ENST00000393153 G2128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr16:30750151 C>T maps to NM_006662.2 L2931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr16:30750151 C>T maps to NM_006662.2 L2931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr16:67693459 G>A maps to NM_001082486.1 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr16:67693459 G>A maps to NM_001082486.1 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr17:7578176 C>T maps to NM_001126112.1 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr17:7578176 C>T maps to NM_001126112.1 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr17:39594346 G>T maps to NM_006771.3 C413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr17:39594346 G>T maps to NM_006771.3 C413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr17:42083544 G>A maps to NM_153006.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr17:42083544 G>A maps to NM_153006.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr17:60501346 G>T maps to NM_181725.3 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr17:60501346 G>T maps to NM_181725.3 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr19:9066781 C>A maps to NM_024690.2 A6888A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr19:9066781 C>A maps to NM_024690.2 A6888A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr19:31769048 G>A maps to NM_020856.2 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr19:31769048 G>A maps to NM_020856.2 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr19:53958192 T>C maps to NM_001008401.3 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr19:53958192 T>C maps to NM_001008401.3 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr19:55378184 A>G maps to ENST00000355608 *456W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr19:55378184 A>G maps to ENST00000355608 *456W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr2:27121504 C>T maps to NM_020134.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr2:27121504 C>T maps to NM_020134.3 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr2:56420318 C>T maps to NM_001080433.1 H328H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr2:56420318 C>T maps to NM_001080433.1 H328H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr2:113331324 C>T maps to NM_019014.4 Q820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr2:113331324 C>T maps to NM_019014.4 Q820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr2:212495210 G>A maps to NM_005235.2 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr2:212495210 G>A maps to NM_005235.2 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr2:228476325 C>T maps to NM_020161.3 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr2:228476325 C>T maps to NM_020161.3 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr20:47296245 G>A maps to NM_020820.3 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr20:47296245 G>A maps to NM_020820.3 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr21:43287418 C>T maps to NM_022115.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr21:43287418 C>T maps to NM_022115.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr3:89478307 T>C maps to NM_005233.5 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr3:89478307 T>C maps to NM_005233.5 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr3:96706229 A>G maps to NM_001080448.2 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr3:96706229 A>G maps to NM_001080448.2 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr4:72215742 A>T maps to NM_001098484.2 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr4:72215742 A>T maps to NM_001098484.2 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr4:126412580 C>A maps to NM_024582.4 P4868P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr4:126412580 C>A maps to NM_024582.4 P4868P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr5:132652309 C>T maps to NM_015082.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr5:132652309 C>T maps to NM_015082.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr6:36020562 C>T maps to NM_139012.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr6:36020562 C>T maps to NM_139012.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr6:132891603 T>C maps to NM_175067.1 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr6:132891603 T>C maps to NM_175067.1 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr7:106508731 C>T maps to NM_002649.2 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr7:106508731 C>T maps to NM_002649.2 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr7:134852540 A>G maps to NM_024033.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr7:134852540 A>G maps to NM_024033.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr8:133622492 G>A maps to ENST00000250173 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr8:133622492 G>A maps to ENST00000250173 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr9:8499727 A>G maps to NM_002839.3 Y747Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr9:8499727 A>G maps to NM_002839.3 Y747Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr9:125154465 A>G did not map to a codon.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr9:125154465 A>G did not map to a codon.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr9:132637881 C>T maps to NM_001008563.3 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr9:132637881 C>T maps to NM_001008563.3 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chrX:51640124 G>A maps to NM_001005333.1 Q514Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chrX:51640124 G>A maps to NM_001005333.1 Q514Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:3754056 G>C maps to NM_014704.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:3754056 G>C maps to NM_014704.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:22919855 G>A maps to NM_020526.3 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:22919855 G>A maps to NM_020526.3 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:22987521 C>A maps to NM_000491.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:22987521 C>A maps to NM_000491.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:23234657 C>A maps to ENST00000400191 A783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:23234657 C>A maps to ENST00000400191 A783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:39763348 A>T maps to ENST00000361689 K810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:39763348 A>T maps to ENST00000361689 K810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:62728767 C>T maps to NM_181712.4 E845E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:62728767 C>T maps to NM_181712.4 E845E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:66036414 C>A maps to NM_002303.5 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:66036414 C>A maps to NM_002303.5 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:110170414 C>A maps to ENST00000393689 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:110170414 C>A maps to ENST00000393689 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:114376997 G>T maps to NM_015967.5 S653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:114376997 G>T maps to NM_015967.5 S653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:115527423 A>T maps to NM_003176.2 K880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:115527423 A>T maps to NM_003176.2 K880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:115828837 G>A maps to NM_002506.2 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:115828837 G>A maps to NM_002506.2 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:153004976 A>G maps to NM_003125.2 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:153004976 A>G maps to NM_003125.2 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:159850453 G>A maps to NM_012337.2 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:159850453 G>A maps to NM_012337.2 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:162724443 G>A maps to NM_006182.2 W72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:162724443 G>A maps to NM_006182.2 W72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:169941739 C>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:169941739 C>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:175049389 C>A maps to NM_022093.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:175049389 C>A maps to NM_022093.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:182354692 T>C did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:182354692 T>C did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:190067932 T>A maps to NM_199051.1 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:190067932 T>A maps to NM_199051.1 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:200826432 G>C did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:200826432 G>C did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:200948799 G>T maps to NM_017596.2 I1328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:200948799 G>T maps to NM_017596.2 I1328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:215847663 G>T maps to ENST00000366943 S4530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:215847663 G>T maps to ENST00000366943 S4530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:237608771 C>A maps to NM_001035.2 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:237608771 C>A maps to NM_001035.2 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:247695519 A>T maps to NM_198074.4 C98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:247695519 A>T maps to NM_198074.4 C98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:247769111 T>C maps to NM_001001914.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:247769111 T>C maps to NM_001001914.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:248309364 G>T maps to NM_001004690.1 G306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:248309364 G>T maps to NM_001004690.1 G306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:248737332 G>A maps to NM_001001821.1 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr1:248737332 G>A maps to NM_001001821.1 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:21108418 C>T maps to ENST00000430741 K663K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:21108418 C>T maps to ENST00000430741 K663K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:27403473 T>C maps to NM_139312.1 E718E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:27403473 T>C maps to NM_139312.1 E718E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:31815598 G>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:31815598 G>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:38242023 T>A maps to NM_145011.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:38242023 T>A maps to NM_145011.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:48438503 G>A maps to NM_004962.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:48438503 G>A maps to NM_004962.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:52575946 G>A maps to NM_138932.2 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:52575946 G>A maps to NM_138932.2 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:56106244 C>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:56106244 C>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:62039398 T>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:62039398 T>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:69961673 C>A maps to NM_032578.2 R1194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:69961673 C>A maps to NM_032578.2 R1194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:76788995 G>T maps to NM_012330.2 E1472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:76788995 G>T maps to NM_012330.2 E1472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:78729806 G>C maps to NM_001161352.1 S762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:78729806 G>C maps to NM_001161352.1 S762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:85944464 C>A maps to NM_207373.2 C63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:85944464 C>A maps to NM_207373.2 C63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:90762892 T>A maps to NM_000043.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:90762892 T>A maps to NM_000043.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:103988897 A>G maps to NM_152310.1 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr10:103988897 A>G maps to NM_152310.1 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:1017713 G>T maps to NM_005961.2 S1696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:1017713 G>T maps to NM_005961.2 S1696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:4608506 C>T maps to NM_001005170.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:4608506 C>T maps to NM_001005170.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:4615654 C>T maps to ENST00000450052 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:4615654 C>T maps to ENST00000450052 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:6191433 G>T maps to NM_001004052.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:6191433 G>T maps to NM_001004052.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:20065573 T>C maps to ENST00000396087 S1008S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:20065573 T>C maps to ENST00000396087 S1008S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:55322573 C>T maps to NM_001001920.1 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:55322573 C>T maps to NM_001001920.1 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:55433551 G>T maps to NM_001004704.1 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:55433551 G>T maps to NM_001004704.1 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:56185378 A>T maps to NM_001004744.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:56185378 A>T maps to NM_001004744.1 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:59829951 C>A maps to NM_006138.4 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:59829951 C>A maps to NM_006138.4 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:64022703 A>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:64022703 A>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:66003367 G>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:66003367 G>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:66392978 A>T maps to NM_006328.3 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:66392978 A>T maps to NM_006328.3 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:67206198 G>T maps to NM_020441.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:67206198 G>T maps to NM_020441.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:82880065 C>T maps to NM_015885.3 Q897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:82880065 C>T maps to NM_015885.3 Q897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:92533402 C>G maps to ENST00000298047 P2408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:92533402 C>G maps to ENST00000298047 P2408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:101344379 C>G maps to NM_004621.5 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:101344379 C>G maps to NM_004621.5 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:101834192 T>C maps to NM_020802.2 N809N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:101834192 T>C maps to NM_020802.2 N809N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:113934660 C>G maps to NM_001018011.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:113934660 C>G maps to NM_001018011.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:118347535 C>A maps to NM_001197104.1 S1058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:118347535 C>A maps to NM_001197104.1 S1058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:120180220 C>A maps to NM_014352.2 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:120180220 C>A maps to NM_014352.2 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:124310450 G>A maps to NM_012378.1 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:124310450 G>A maps to NM_012378.1 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:124765698 C>G maps to NM_019055.5 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:124765698 C>G maps to NM_019055.5 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:130773226 T>C maps to NM_014758.2 L832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:130773226 T>C maps to NM_014758.2 L832L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:133794769 G>T maps to NM_014987.1 A688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr11:133794769 G>T maps to NM_014987.1 A688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:11034875 C>A maps to NM_006250.2 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:11034875 C>A maps to NM_006250.2 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:14796619 G>T maps to NM_004963.3 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:14796619 G>T maps to NM_004963.3 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:18435605 T>C maps to NM_004570.4 H197H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:18435605 T>C maps to NM_004570.4 H197H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:21349913 G>A maps to NM_006446.4 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:21349913 G>A maps to NM_006446.4 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:29631792 T>C maps to NM_183378.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:29631792 T>C maps to NM_183378.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:53227939 T>C maps to NM_175834.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:53227939 T>C maps to NM_175834.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:56429105 G>A maps to NM_022465.3 K583K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:56429105 G>A maps to NM_022465.3 K583K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:60173399 T>C maps to NM_004731.3 D459D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:60173399 T>C maps to NM_004731.3 D459D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:63543950 G>T maps to NM_000706.3 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:63543950 G>T maps to NM_000706.3 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:78400499 G>C maps to NM_014903.4 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:78400499 G>C maps to NM_014903.4 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:81627153 T>C maps to NM_024560.2 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:81627153 T>C maps to NM_024560.2 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:85255710 G>T maps to NM_182767.4 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:85255710 G>T maps to NM_182767.4 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:96312653 C>A maps to NM_182496.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:96312653 C>A maps to NM_182496.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:101603613 G>T maps to NM_145913.3 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:101603613 G>T maps to NM_145913.3 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:106466567 C>G maps to NM_014840.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:106466567 C>G maps to NM_014840.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:108029159 G>C maps to NM_001018072.1 S910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:108029159 G>C maps to NM_001018072.1 S910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:108930561 C>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:108930561 C>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:109650675 G>C maps to NM_001093.3 L1095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:109650675 G>C maps to NM_001093.3 L1095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:120114376 G>T maps to NM_006253.4 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:120114376 G>T maps to NM_006253.4 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:122825410 C>T maps to ENST00000302528 R780R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:122825410 C>T maps to ENST00000302528 R780R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:124383261 G>T maps to NM_207437.3 E3063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:124383261 G>T maps to NM_207437.3 E3063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:131466552 G>A maps to NM_198827.3 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:131466552 G>A maps to NM_198827.3 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:133225972 C>A maps to ENST00000455752 R1311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:133225972 C>A maps to ENST00000455752 R1311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:133257866 T>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:133257866 T>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:133733347 A>T maps to NM_015394.4 K506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr12:133733347 A>T maps to NM_015394.4 K506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr13:25671149 C>A maps to NM_030979.2 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr13:25671149 C>A maps to NM_030979.2 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr13:49281444 C>A maps to NM_020377.2 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr13:49281444 C>A maps to NM_020377.2 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:20248501 C>A maps to NM_001005500.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:20248501 C>A maps to NM_001005500.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:20482728 G>C maps to NM_001004712.1 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:20482728 G>C maps to NM_001004712.1 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:20528985 A>G maps to NM_001004717.1 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:20528985 A>G maps to NM_001004717.1 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:20666321 C>T maps to NM_001005503.1 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:20666321 C>T maps to NM_001005503.1 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:45669147 T>C maps to NM_020937.2 Y2028Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:45669147 T>C maps to NM_020937.2 Y2028Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:69257125 C>A maps to NM_004926.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:69257125 C>A maps to NM_004926.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:86087867 C>T maps to NM_013231.4 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:86087867 C>T maps to NM_013231.4 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:86088277 G>C maps to NM_013231.4 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:86088277 G>C maps to NM_013231.4 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:91948114 T>A maps to ENST00000417249 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr14:91948114 T>A maps to ENST00000417249 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr15:23931752 G>T maps to NM_002487.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr15:23931752 G>T maps to NM_002487.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr15:70351091 G>A maps to NM_005078.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr15:70351091 G>A maps to NM_005078.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr15:76171513 T>G maps to NM_173469.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr15:76171513 T>G maps to NM_173469.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr16:2167055 T>C did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr16:2167055 T>C did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr16:2329014 C>T maps to NM_001089.2 G1492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr16:2329014 C>T maps to NM_001089.2 G1492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr16:3306442 T>G maps to NM_000243.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr16:3306442 T>G maps to NM_000243.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr16:20442555 G>A maps to NM_017888.2 E407E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr16:20442555 G>A maps to NM_017888.2 E407E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr16:20948069 C>T maps to NM_017539.1 V3920V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr16:20948069 C>T maps to NM_017539.1 V3920V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr16:51175025 C>G maps to ENST00000251020 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr16:51175025 C>G maps to ENST00000251020 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr16:69377540 G>A maps to NM_144676.3 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr16:69377540 G>A maps to NM_144676.3 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:7689566 C>T maps to NM_020877.2 C2085C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:7689566 C>T maps to NM_020877.2 C2085C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:10354159 G>T maps to NM_017533.2 S1306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:10354159 G>T maps to NM_017533.2 S1306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:12620738 G>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:12620738 G>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:21318737 C>T maps to NM_021012.4 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:21318737 C>T maps to NM_021012.4 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:35468547 T>G maps to NM_198834.1 V2161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:35468547 T>G maps to NM_198834.1 V2161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:61843412 T>C maps to NM_020198.2 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:61843412 T>C maps to NM_020198.2 E41E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:66871843 C>G maps to NM_007168.2 T1427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr17:66871843 C>G maps to NM_007168.2 T1427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr18:5891786 C>T maps to NM_001080209.1 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr18:5891786 C>T maps to NM_001080209.1 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr18:31323687 C>A maps to NM_030632.1 C1292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr18:31323687 C>A maps to NM_030632.1 C1292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr18:48439272 G>T maps to NM_002396.4 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr18:48439272 G>T maps to NM_002396.4 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr18:51013296 G>T maps to NM_005215.3 V1289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr18:51013296 G>T maps to NM_005215.3 V1289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:541374 T>C maps to NM_004359.1 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:541374 T>C maps to NM_004359.1 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:5082395 G>T maps to NM_015015.2 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:5082395 G>T maps to NM_015015.2 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:7999065 C>A maps to NM_006351.3 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:7999065 C>A maps to NM_006351.3 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:9071926 A>G maps to NM_024690.2 G5173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:9071926 A>G maps to NM_024690.2 G5173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:10475628 C>T maps to NM_003331.4 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:10475628 C>T maps to NM_003331.4 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:11144852 G>T maps to NM_001128849.1 E1310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:11144852 G>T maps to NM_001128849.1 E1310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:12256681 T>A maps to ENST00000439556 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:12256681 T>A maps to ENST00000439556 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:24309075 C>T maps to NM_203282.2 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:24309075 C>T maps to NM_203282.2 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:36357123 T>C maps to NM_199180.2 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:36357123 T>C maps to NM_199180.2 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:38956796 G>C maps to NM_000540.2 A979A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:38956796 G>C maps to NM_000540.2 A979A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:40886622 G>T maps to NM_144685.3 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:40886622 G>T maps to NM_144685.3 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:41516002 C>T maps to NM_000767.4 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:41516002 C>T maps to NM_000767.4 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:44051049 T>A maps to NM_006297.2 K427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:44051049 T>A maps to NM_006297.2 K427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:46290015 G>A maps to NM_004943.1 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:46290015 G>A maps to NM_004943.1 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:50364537 C>A maps to NM_007254.3 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:50364537 C>A maps to NM_007254.3 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:51274591 G>T maps to NM_001506.1 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:51274591 G>T maps to NM_001506.1 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:54401340 T>C maps to NM_002739.3 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:54401340 T>C maps to NM_002739.3 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:54742903 G>T maps to NM_024318.2 V457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:54742903 G>T maps to NM_024318.2 V457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:55417663 T>A maps to NM_004829.5 C14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:55417663 T>A maps to NM_004829.5 C14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:56370016 C>A maps to NM_134444.4 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:56370016 C>A maps to NM_134444.4 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:56372753 C>A maps to NM_134444.4 S620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:56372753 C>A maps to NM_134444.4 S620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:58967711 G>T maps to NM_207395.2 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr19:58967711 G>T maps to NM_207395.2 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:1658259 C>A maps to NM_012293.1 G620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:1658259 C>A maps to NM_012293.1 G620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:1680769 C>T maps to NM_012293.1 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:1680769 C>T maps to NM_012293.1 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:1914013 G>A maps to ENST00000399161 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:1914013 G>A maps to ENST00000399161 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:32474681 G>A maps to NM_021209.4 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:32474681 G>A maps to NM_021209.4 L751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:32475966 C>T maps to NM_021209.4 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:32475966 C>T maps to NM_021209.4 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:33540328 G>A maps to ENST00000354476 T1242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:33540328 G>A maps to ENST00000354476 T1242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:33741636 T>C maps to NM_170672.2 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:33741636 T>C maps to NM_170672.2 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:50779851 C>T maps to ENST00000404971 E584E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:50779851 C>T maps to ENST00000404971 E584E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:71797808 C>T maps to NM_001130987.1 R1056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:71797808 C>T maps to NM_001130987.1 R1056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:73315800 C>G maps to NM_015470.2 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:73315800 C>G maps to NM_015470.2 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:74709691 G>A maps to ENST00000393965 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:74709691 G>A maps to ENST00000393965 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:80816526 C>G maps to ENST00000402739 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:80816526 C>G maps to ENST00000402739 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:86350829 G>T maps to NM_017952.5 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:86350829 G>T maps to NM_017952.5 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:96780850 C>A maps to NM_000682.5 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:96780850 C>A maps to NM_000682.5 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:102000149 T>C maps to NM_153836.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:102000149 T>C maps to NM_153836.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:112944821 G>T maps to NM_153214.2 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:112944821 G>T maps to NM_153214.2 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:114503856 A>T maps to NM_025181.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:114503856 A>T maps to NM_025181.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:168105476 A>T maps to NM_152381.5 P2525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:168105476 A>T maps to NM_152381.5 P2525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:170096253 A>T maps to NM_004525.2 G1359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:170096253 A>T maps to NM_004525.2 G1359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:170667534 A>G maps to NM_003142.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:170667534 A>G maps to NM_003142.3 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:179392224 A>G maps to NM_133378.4 N33308N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:179392224 A>G maps to NM_133378.4 N33308N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:179482515 A>T maps to NM_133378.4 A13286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:179482515 A>T maps to NM_133378.4 A13286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:189854842 C>A maps to NM_000090.3 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:189854842 C>A maps to NM_000090.3 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:202137358 A>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:202137358 A>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:215976317 A>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr2:215976317 A>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr20:14306910 A>C maps to NM_198391.2 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr20:14306910 A>C maps to NM_198391.2 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr20:23860132 T>A maps to NM_001900.4 K61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr20:23860132 T>A maps to NM_001900.4 K61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr20:31601614 G>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr20:31601614 G>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr20:31601639 G>C maps to NM_025227.1 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr20:31601639 G>C maps to NM_025227.1 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr20:42328422 C>T maps to NM_002466.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr20:42328422 C>T maps to NM_002466.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr20:57268860 C>T maps to NM_024663.3 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr20:57268860 C>T maps to NM_024663.3 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr21:31797759 C>T maps to NM_181622.1 W157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr21:31797759 C>T maps to NM_181622.1 W157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr22:24480530 G>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr22:24480530 G>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr22:40417674 C>T maps to NM_138435.2 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr22:40417674 C>T maps to NM_138435.2 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr22:50315315 C>A maps to NM_001135101.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr22:50315315 C>A maps to NM_001135101.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:14939484 G>A maps to NM_152536.3 R983R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:14939484 G>A maps to NM_152536.3 R983R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:21465511 G>T maps to NM_024697.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:21465511 G>T maps to NM_024697.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:21606086 G>T maps to NM_024697.2 C85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:21606086 G>T maps to NM_024697.2 C85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:38763807 C>A maps to NM_006514.2 E1150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:38763807 C>A maps to NM_006514.2 E1150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:39374448 C>T maps to NM_005201.3 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:39374448 C>T maps to NM_005201.3 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:47618789 C>T maps to ENST00000383738 E242E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:47618789 C>T maps to ENST00000383738 E242E. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CR-7402-01A-11D-2012-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-CR-7402-01A-11D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:119301304 C>A maps to NM_001125.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:119301304 C>A maps to NM_001125.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:121838296 T>C maps to NM_175862.3 H302H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:121838296 T>C maps to NM_175862.3 H302H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:123427704 C>A maps to NM_053025.3 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:123427704 C>A maps to NM_053025.3 G660G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CR-7402-01A-11D-2012-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-CR-7402-01A-11D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:126291215 C>A maps to NM_001039783.1 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:126291215 C>A maps to NM_001039783.1 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:128060073 A>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:128060073 A>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:130442378 C>G maps to NM_014602.2 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:130442378 C>G maps to NM_014602.2 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:130683849 T>A maps to NM_001001486.1 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:130683849 T>A maps to NM_001001486.1 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:172059018 C>T maps to NM_022763.3 Q657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:172059018 C>T maps to NM_022763.3 Q657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:182841970 C>A maps to NM_014398.3 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:182841970 C>A maps to NM_014398.3 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:182924002 C>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:182924002 C>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:190326879 G>T maps to NM_002182.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:190326879 G>T maps to NM_002182.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:191179205 T>G maps to NM_001083308.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:191179205 T>G maps to NM_001083308.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:195012436 T>A maps to NM_012287.5 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr3:195012436 T>A maps to NM_012287.5 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:5527952 C>T maps to NM_005750.2 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:5527952 C>T maps to NM_005750.2 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:13605782 G>T maps to NM_148894.2 S914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:13605782 G>T maps to NM_148894.2 S914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:20568975 C>T maps to ENST00000273739 D943D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:20568975 C>T maps to ENST00000273739 D943D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:25314460 C>A maps to NM_024936.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:25314460 C>A maps to NM_024936.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:30725161 C>T maps to NM_001173523.1 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:30725161 C>T maps to NM_001173523.1 T706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:37903766 C>A maps to NM_015173.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:37903766 C>A maps to NM_015173.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:74318194 T>A maps to NM_001134.1 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:74318194 T>A maps to NM_001134.1 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:96761795 C>A maps to NM_005390.4 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:96761795 C>A maps to NM_005390.4 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:102951360 C>A maps to NM_017935.4 A613A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:102951360 C>A maps to NM_017935.4 A613A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:114274327 C>A maps to NM_001148.4 T1518T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:114274327 C>A maps to NM_001148.4 T1518T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:143235900 G>T maps to NM_003866.2 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr4:143235900 G>T maps to NM_003866.2 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:33457372 G>A maps to ENST00000455217 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:33457372 G>A maps to ENST00000455217 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:33643536 A>G maps to NM_030955.2 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:33643536 A>G maps to NM_030955.2 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:37181061 C>A maps to NM_023073.3 E1823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:37181061 C>A maps to NM_023073.3 E1823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:38438423 C>T maps to ENST00000354891 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:38438423 C>T maps to ENST00000354891 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:54945035 T>C maps to NM_173514.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:54945035 T>C maps to NM_173514.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:72427520 A>T maps to NM_173490.6 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:72427520 A>T maps to NM_173490.6 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:89930998 C>T maps to NM_032119.3 I636I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:89930998 C>T maps to NM_032119.3 I636I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:89954096 T>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:89954096 T>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:99871503 G>T maps to NM_198507.1 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:99871503 G>T maps to NM_198507.1 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:101606490 C>T maps to NM_180991.4 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:101606490 C>T maps to NM_180991.4 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:114573586 C>G maps to NM_005023.3 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:114573586 C>G maps to NM_005023.3 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:115336168 G>T maps to NM_173800.4 E519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:115336168 G>T maps to NM_173800.4 E519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:121187729 C>T maps to NM_177478.1 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:121187729 C>T maps to NM_177478.1 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:131953938 A>T maps to NM_005732.3 T1114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:131953938 A>T maps to NM_005732.3 T1114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:135394833 G>T maps to NM_000358.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:135394833 G>T maps to NM_000358.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:140167950 G>A maps to NM_018900.2 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:140167950 G>A maps to NM_018900.2 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:140182401 G>T maps to NM_018906.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:140182401 G>T maps to NM_018906.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:140203531 G>T maps to NM_018908.2 A724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:140203531 G>T maps to NM_018908.2 A724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:140433331 A>T maps to NM_013340.2 S759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:140433331 A>T maps to NM_013340.2 S759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:140481906 G>C maps to NM_018937.2 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:140481906 G>C maps to NM_018937.2 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:148407062 C>A maps to NM_024577.3 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:148407062 C>A maps to NM_024577.3 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:149678015 A>G maps to NM_001012301.2 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:149678015 A>G maps to NM_001012301.2 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:156899364 G>A maps to NM_001099287.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:156899364 G>A maps to NM_001099287.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:156929849 A>T maps to ENST00000430702 Y425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:156929849 A>T maps to ENST00000430702 Y425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:157181900 G>T maps to NM_173491.2 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:157181900 G>T maps to NM_173491.2 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:160071163 A>G maps to NM_025153.2 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:160071163 A>G maps to NM_025153.2 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:169454880 C>T maps to NM_004946.2 I1132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:169454880 C>T maps to NM_004946.2 I1132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:176709537 C>T maps to NM_022455.4 Q1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:176709537 C>T maps to NM_022455.4 Q1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:178503531 G>T maps to NM_014594.1 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr5:178503531 G>T maps to NM_014594.1 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:24533786 G>A maps to NM_170740.1 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:24533786 G>A maps to NM_170740.1 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:29080329 T>A maps to NM_001005216.2 Y221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:29080329 T>A maps to NM_001005216.2 Y221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:32122554 G>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:32122554 G>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:33262942 C>T maps to NM_004761.3 E390E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:33262942 C>T maps to NM_004761.3 E390E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:36766230 C>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:36766230 C>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:38885915 G>A maps to ENST00000327475 K3496K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:38885915 G>A maps to ENST00000327475 K3496K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:54214630 C>T maps to NM_014464.3 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:54214630 C>T maps to NM_014464.3 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:75893060 C>T maps to ENST00000322507 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:75893060 C>T maps to ENST00000322507 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:84350841 T>C maps to NM_014841.2 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:84350841 T>C maps to NM_014841.2 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:107069362 C>T maps to NM_032730.4 W144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:107069362 C>T maps to NM_032730.4 W144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:130535480 C>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:130535480 C>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:138576846 C>A maps to NM_020340.4 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:138576846 C>A maps to NM_020340.4 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:144263313 T>C maps to NM_001080951.1 K213K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:144263313 T>C maps to NM_001080951.1 K213K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:152382207 C>T maps to NM_001122741.1 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:152382207 C>T maps to NM_001122741.1 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:158569895 C>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:158569895 C>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:166571921 C>A maps to NM_003181.2 G397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr6:166571921 C>A maps to NM_003181.2 G397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:4091358 G>C maps to NM_152744.3 T936T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:4091358 G>C maps to NM_152744.3 T936T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:7278537 T>A maps to NM_020156.3 Y291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:7278537 T>A maps to NM_020156.3 Y291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:31890355 C>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:31890355 C>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:35673919 A>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:35673919 A>G did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:37903046 C>A maps to NM_016616.4 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:37903046 C>A maps to NM_016616.4 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:40498770 A>G maps to NM_001193311.1 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:40498770 A>G maps to NM_001193311.1 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:47408664 G>T maps to NM_022748.11 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:47408664 G>T maps to NM_022748.11 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:47474984 C>T maps to NM_022748.11 W73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:47474984 C>T maps to NM_022748.11 W73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:50070686 C>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:50070686 C>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:82451862 C>A maps to NM_033026.5 G4913G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:82451862 C>A maps to NM_033026.5 G4913G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:92134133 C>A maps to NM_000466.2 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:92134133 C>A maps to NM_000466.2 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:94944745 A>G maps to NM_000446.5 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:94944745 A>G maps to NM_000446.5 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:99097389 C>T maps to NM_032164.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:99097389 C>T maps to NM_032164.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:100676772 T>C maps to NM_001040105.1 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:100676772 T>C maps to NM_001040105.1 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:107746423 A>G maps to NM_007356.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:107746423 A>G maps to NM_007356.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:110762956 C>A maps to NM_018334.4 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:110762956 C>A maps to NM_018334.4 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:123508734 A>G maps to NM_012269.2 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:123508734 A>G maps to NM_012269.2 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:127223057 C>T maps to NM_024523.5 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:127223057 C>T maps to NM_024523.5 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:137271842 C>A maps to NM_004717.2 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:137271842 C>A maps to NM_004717.2 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:139756946 G>A maps to NM_022750.2 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:139756946 G>A maps to NM_022750.2 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:143747688 G>T maps to NM_012365.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:143747688 G>T maps to NM_012365.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:143793099 A>G maps to NM_001004135.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:143793099 A>G maps to NM_001004135.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:149462861 G>A maps to NM_207336.1 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr7:149462861 G>A maps to NM_207336.1 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:22675245 G>T maps to NM_144962.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:22675245 G>T maps to NM_144962.2 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:25715904 G>T maps to NM_022659.2 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:25715904 G>T maps to NM_022659.2 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:37914653 G>T maps to NM_004095.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:37914653 G>T maps to NM_004095.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:52384808 G>T maps to NM_144651.4 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:52384808 G>T maps to NM_144651.4 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:55537479 C>T maps to NM_006269.1 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:55537479 C>T maps to NM_006269.1 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:66605982 A>T maps to NM_014637.3 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:66605982 A>T maps to NM_014637.3 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:77775783 C>A maps to NM_024721.4 L3278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:77775783 C>A maps to NM_024721.4 L3278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:81605275 A>C maps to NM_001033723.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:81605275 A>C maps to NM_001033723.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:88885722 G>T maps to NM_152418.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:88885722 G>T maps to NM_152418.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:95161032 C>T maps to NM_001144663.1 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:95161032 C>T maps to NM_001144663.1 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:110980753 C>A maps to NM_014379.2 G356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:110980753 C>A maps to NM_014379.2 G356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:131861991 G>C maps to NM_001115.2 V756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:131861991 G>C maps to NM_001115.2 V756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:133816971 T>G maps to ENST00000395386 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:133816971 T>G maps to ENST00000395386 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:134050882 C>A maps to NM_006748.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr8:134050882 C>A maps to NM_006748.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:5757414 T>C maps to ENST00000414202 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:5757414 T>C maps to ENST00000414202 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:26905640 A>G maps to NM_001031689.2 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:26905640 A>G maps to NM_001031689.2 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:33799063 C>G maps to NM_007343.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:33799063 C>G maps to NM_007343.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:35557971 G>T maps to NM_001135999.1 R1015R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:35557971 G>T maps to NM_001135999.1 R1015R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:35609310 C>T maps to NM_006285.2 Q485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:35609310 C>T maps to NM_006285.2 Q485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:35809451 C>A maps to NM_172312.1 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:35809451 C>A maps to NM_172312.1 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:79635322 G>T maps to NM_001013735.1 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:79635322 G>T maps to NM_001013735.1 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:96025976 G>T maps to ENST00000297954 R1180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:96025976 G>T maps to ENST00000297954 R1180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:105765546 T>C did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:105765546 T>C did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:107379789 C>T maps to NM_001001956.1 E232E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:107379789 C>T maps to NM_001001956.1 E232E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:117849087 C>A maps to NM_002160.2 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:117849087 C>A maps to NM_002160.2 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:118950330 G>T maps to NM_002581.3 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:118950330 G>T maps to NM_002581.3 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:122075567 G>A maps to NM_014618.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:122075567 G>A maps to NM_014618.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:125154750 C>A maps to NM_000962.2 Y576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:125154750 C>A maps to NM_000962.2 Y576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:130506940 G>T maps to NM_170600.2 R568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:130506940 G>T maps to NM_170600.2 R568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:133946977 G>A maps to ENST00000355048 R1059R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:133946977 G>A maps to ENST00000355048 R1059R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:134394276 G>A maps to NM_007171.3 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:134394276 G>A maps to NM_007171.3 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:136226862 T>C maps to NM_017503.3 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr9:136226862 T>C maps to NM_017503.3 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chrX:27839500 A>T maps to NM_182506.3 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chrX:27839500 A>T maps to NM_182506.3 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chrX:49142666 G>A maps to NM_033215.4 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chrX:49142666 G>A maps to NM_033215.4 A505A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chrX:50052854 T>A maps to NM_033031.2 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chrX:50052854 T>A maps to NM_033031.2 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chrX:125686093 G>T maps to NM_178470.4 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chrX:125686093 G>T maps to NM_178470.4 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chrX:140785675 G>T maps to NM_145665.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chrX:140785675 G>T maps to NM_145665.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chrX:141291746 G>A maps to NM_016249.3 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chrX:141291746 G>A maps to NM_016249.3 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chrY:6736362 G>T maps to ENST00000383036 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chrY:6736362 G>T maps to ENST00000383036 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:11775203 C>G maps to NM_198545.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:11775203 C>G maps to NM_198545.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:21268029 C>T maps to NM_001198801.1 E482E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:21268029 C>T maps to NM_001198801.1 E482E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CR-7404-01A-11D-2129-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CR-7404-01A-11D-2129-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:47282749 C>G maps to NM_001099772.1 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:47282749 C>G maps to NM_001099772.1 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:155720452 A>G maps to ENST00000368331 D2216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:155720452 A>G maps to ENST00000368331 D2216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:161495704 C>T maps to NM_002155.3 N419N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:161495704 C>T maps to NM_002155.3 N419N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:168037615 C>T maps to ENST00000367840 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:168037615 C>T maps to ENST00000367840 L902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:179013305 G>A maps to NM_014864.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:179013305 G>A maps to NM_014864.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:247752500 C>T maps to NM_001001915.1 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr1:247752500 C>T maps to NM_001001915.1 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr10:32582603 C>T maps to NM_025209.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr10:32582603 C>T maps to NM_025209.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr10:37421250 G>C maps to ENST00000374660 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr10:37421250 G>C maps to ENST00000374660 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr11:70331426 G>A maps to ENST00000338508 L1651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr11:70331426 G>A maps to ENST00000338508 L1651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr11:75316986 C>T maps to NM_033063.1 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr11:75316986 C>T maps to NM_033063.1 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr12:50186312 G>A maps to NM_001037806.3 F1236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr12:50186312 G>A maps to NM_001037806.3 F1236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr12:117977626 C>T maps to ENST00000339824 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr12:117977626 C>T maps to ENST00000339824 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr12:124330338 C>T maps to NM_207437.3 N1733N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr12:124330338 C>T maps to NM_207437.3 N1733N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr13:38320193 C>T maps to NM_003306.1 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr13:38320193 C>T maps to NM_003306.1 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr13:110827072 G>A maps to NM_001845.4 F1074F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr13:110827072 G>A maps to NM_001845.4 F1074F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr14:52794008 C>G maps to NM_000956.3 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr14:52794008 C>G maps to NM_000956.3 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr15:85328023 C>T maps to NM_014630.2 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr15:85328023 C>T maps to NM_014630.2 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr16:1470387 G>A maps to NM_001010878.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr16:1470387 G>A maps to NM_001010878.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr16:19085307 C>G maps to NM_016138.4 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr16:19085307 C>G maps to NM_016138.4 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr16:49672147 G>A maps to NM_015069.2 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr16:49672147 G>A maps to NM_015069.2 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr17:11520896 G>A maps to NM_001372.3 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr17:11520896 G>A maps to NM_001372.3 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr17:80363225 G>A maps to NM_175902.4 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr17:80363225 G>A maps to NM_175902.4 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr18:8784807 G>C maps to ENST00000456698 G926G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr18:8784807 G>C maps to ENST00000456698 G926G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr19:327203 G>T maps to NM_017550.1 S141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr19:327203 G>T maps to NM_017550.1 S141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr19:4359197 C>T maps to ENST00000262967 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr19:4359197 C>T maps to ENST00000262967 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr2:152521101 C>T maps to NM_001164507.1 W1788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr2:152521101 C>T maps to NM_001164507.1 W1788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr2:162735687 G>A maps to NM_001178015.1 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr2:162735687 G>A maps to NM_001178015.1 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr2:168106862 G>C maps to NM_152381.5 L2987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr2:168106862 G>C maps to NM_152381.5 L2987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr2:228882640 G>A maps to NM_001142644.1 R977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr2:228882640 G>A maps to NM_001142644.1 R977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr20:468205 G>A maps to NM_177559.2 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr20:468205 G>A maps to NM_177559.2 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr21:44450049 C>T maps to NM_004571.3 Q384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr21:44450049 C>T maps to NM_004571.3 Q384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr22:28193510 C>T maps to NM_002430.2 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr22:28193510 C>T maps to NM_002430.2 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr3:24018765 C>T maps to NM_005126.4 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr3:24018765 C>T maps to NM_005126.4 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr3:164754186 T>C maps to NM_001041.3 G835G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr3:164754186 T>C maps to NM_001041.3 G835G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr3:195608989 C>T maps to NM_001010938.1 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr3:195608989 C>T maps to NM_001010938.1 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr5:131822223 T>C did not map to a codon.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr5:131822223 T>C did not map to a codon.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr6:31646944 G>A maps to NM_025262.3 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr6:31646944 G>A maps to NM_025262.3 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr7:43519315 G>A maps to NM_015052.3 Q1069Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr7:43519315 G>A maps to NM_015052.3 Q1069Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr7:88423629 G>C maps to NM_152706.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr7:88423629 G>C maps to NM_152706.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr8:61764695 G>A maps to NM_017780.2 Q1928Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr8:61764695 G>A maps to NM_017780.2 Q1928Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr9:80856705 G>A maps to NM_001098802.1 K198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chr9:80856705 G>A maps to NM_001098802.1 K198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chrX:13645319 G>A maps to NM_001167890.1 E493E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chrX:13645319 G>A maps to NM_001167890.1 E493E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chrX:70470532 G>A maps to ENST00000373988 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chrX:70470532 G>A maps to ENST00000373988 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chrX:102471380 G>A maps to NM_001080425.2 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chrX:102471380 G>A maps to NM_001080425.2 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chrX:118370415 C>T maps to NM_006667.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7404-01A-11D-2129-08 chrX:118370415 C>T maps to NM_006667.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr1:47882289 C>T maps to NM_012186.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr1:47882289 C>T maps to NM_012186.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr1:109554139 G>T maps to NM_001142550.1 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr1:109554139 G>T maps to NM_001142550.1 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr1:156884445 C>T maps to NM_001080471.1 D990D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr1:156884445 C>T maps to NM_001080471.1 D990D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr1:157666928 C>G did not map to a codon.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr1:157666928 C>G did not map to a codon.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr1:171509613 A>G maps to ENST00000392078 R1003R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr1:171509613 A>G maps to ENST00000392078 R1003R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr1:176668353 G>T maps to NM_020318.2 L955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr1:176668353 G>T maps to NM_020318.2 L955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr1:180165520 C>G maps to NM_002826.4 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr1:180165520 C>G maps to NM_002826.4 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr10:90682923 G>C did not map to a codon.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr10:90682923 G>C did not map to a codon.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr10:127429568 G>C did not map to a codon.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr10:127429568 G>C did not map to a codon.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr11:22363085 G>A maps to NM_020346.2 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr11:22363085 G>A maps to NM_020346.2 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr12:9095068 T>C maps to NM_002355.2 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr12:9095068 T>C maps to NM_002355.2 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr12:53663847 G>A maps to NM_012291.4 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr12:53663847 G>A maps to NM_012291.4 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr12:54448754 C>A maps to NM_153633.2 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr12:54448754 C>A maps to NM_153633.2 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr12:56143302 T>C maps to NM_005811.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr12:56143302 T>C maps to NM_005811.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr12:121426776 G>A maps to NM_000545.5 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr12:121426776 G>A maps to NM_000545.5 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr14:24789047 G>C maps to NM_139247.3 S878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr14:24789047 G>C maps to NM_139247.3 S878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr15:40750962 C>G maps to NM_014952.3 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr15:40750962 C>G maps to NM_014952.3 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr16:615180 C>G maps to ENST00000293874 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr16:615180 C>G maps to ENST00000293874 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr16:4934902 G>C maps to NM_002705.4 L1251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr16:4934902 G>C maps to NM_002705.4 L1251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr16:20781559 G>A maps to NM_005622.3 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr16:20781559 G>A maps to NM_005622.3 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr17:3301356 C>T maps to NM_003553.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr17:3301356 C>T maps to NM_003553.2 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr17:5486122 C>T maps to NM_033004.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr17:5486122 C>T maps to NM_033004.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr17:7667310 C>G maps to NM_020877.2 L1047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr17:7667310 C>G maps to NM_020877.2 L1047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr17:10545559 G>A maps to NM_002470.2 F652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr17:10545559 G>A maps to NM_002470.2 F652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr18:56184166 G>T maps to NM_052947.3 I1971I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr18:56184166 G>T maps to NM_052947.3 I1971I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr18:58038765 G>A maps to NM_005912.2 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr18:58038765 G>A maps to NM_005912.2 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr19:2096976 G>T maps to NM_001039846.1 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr19:2096976 G>T maps to NM_001039846.1 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr19:4171168 C>T maps to NM_032607.1 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr19:4171168 C>T maps to NM_032607.1 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr19:23836954 T>C maps to NM_138330.2 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr19:23836954 T>C maps to NM_138330.2 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr19:45316586 C>G maps to NM_005581.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr19:45316586 C>G maps to NM_005581.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr19:52619846 A>G maps to NM_178523.3 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr19:52619846 A>G maps to NM_178523.3 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr2:9666272 G>A maps to NM_003183.4 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr2:9666272 G>A maps to NM_003183.4 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr2:54155436 T>C maps to NM_014614.2 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr2:54155436 T>C maps to NM_014614.2 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr2:201798697 C>T did not map to a codon.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr2:201798697 C>T did not map to a codon.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr20:25199203 G>A maps to NM_001247.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr20:25199203 G>A maps to NM_001247.2 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr20:60511841 C>T maps to NM_001794.2 S864S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr20:60511841 C>T maps to NM_001794.2 S864S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr22:29695244 C>T maps to NM_013986.3 F539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr22:29695244 C>T maps to NM_013986.3 F539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr22:30722696 G>A maps to ENST00000403477 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr22:30722696 G>A maps to ENST00000403477 F58F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr3:53834347 G>T maps to NM_001128840.1 E1666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr3:53834347 G>T maps to NM_001128840.1 E1666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr3:57542168 G>A maps to NM_177966.5 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr3:57542168 G>A maps to NM_177966.5 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr3:130715583 C>G maps to NM_001001486.1 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr3:130715583 C>G maps to NM_001001486.1 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr3:134323140 G>A maps to NM_178554.4 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr3:134323140 G>A maps to NM_178554.4 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr4:9828062 G>A maps to NM_020041.2 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr4:9828062 G>A maps to NM_020041.2 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr4:74846998 C>T maps to NM_002619.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr4:74846998 C>T maps to NM_002619.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr4:187538163 C>A maps to ENST00000260147 E3027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr4:187538163 C>A maps to ENST00000260147 E3027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr5:167887708 C>T maps to NM_001161661.1 R960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr5:167887708 C>T maps to NM_001161661.1 R960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr6:42036203 G>A maps to NM_138572.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr6:42036203 G>A maps to NM_138572.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr6:94120309 C>T maps to NM_004440.3 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr6:94120309 C>T maps to NM_004440.3 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr7:47882700 G>T maps to NM_138295.3 V1768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr7:47882700 G>T maps to NM_138295.3 V1768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr7:90895580 C>T maps to NM_003505.1 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr7:90895580 C>T maps to NM_003505.1 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr7:151798007 T>C did not map to a codon.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr7:151798007 T>C did not map to a codon.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr8:19315938 G>A maps to NM_018371.4 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr8:19315938 G>A maps to NM_018371.4 F283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr8:24813612 G>C maps to ENST00000221169 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr8:24813612 G>C maps to ENST00000221169 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr8:141874415 G>A maps to NM_005607.4 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr8:141874415 G>A maps to NM_005607.4 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr9:116136273 G>A maps to NM_031219.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr9:116136273 G>A maps to NM_031219.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chrX:100547853 G>A maps to NM_024885.3 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chrX:100547853 G>A maps to NM_024885.3 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chrX:148798057 T>C maps to NM_005366.4 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chrX:148798057 T>C maps to NM_005366.4 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr16:2053039 C>T maps to ENST00000431526 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr16:2053039 C>T maps to ENST00000431526 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr17:39183230 A>G maps to NM_031957.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5430-01A-02D-1683-08 chr17:39183230 A>G maps to NM_031957.1 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:19029672 C>T maps to NM_002584.2 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:19029672 C>T maps to NM_002584.2 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:32542919 G>A did not map to a codon.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:32542919 G>A did not map to a codon.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:42880191 C>T maps to NM_173642.3 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:42880191 C>T maps to NM_173642.3 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:43830979 G>A maps to NM_022821.2 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:43830979 G>A maps to NM_022821.2 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:90400811 C>T maps to NM_001134479.1 Q729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:90400811 C>T maps to NM_001134479.1 Q729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:158226597 C>G maps to NM_001763.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:158226597 C>G maps to NM_001763.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:158615001 G>A maps to NM_003126.2 I1390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:158615001 G>A maps to NM_003126.2 I1390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:162748506 C>T maps to NM_006182.2 D807D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:162748506 C>T maps to NM_006182.2 D807D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:166905900 C>T maps to NM_199351.2 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:166905900 C>T maps to NM_199351.2 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:248004601 G>A maps to NM_001001959.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr1:248004601 G>A maps to NM_001001959.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr11:124743755 C>T maps to NM_022370.3 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr11:124743755 C>T maps to NM_022370.3 F594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr12:12966312 C>T maps to NM_016355.3 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr12:12966312 C>T maps to NM_016355.3 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr12:32895603 A>G maps to ENST00000381000 K705K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr12:32895603 A>G maps to ENST00000381000 K705K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr13:76391320 C>T maps to ENST00000357063 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr13:76391320 C>T maps to ENST00000357063 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr15:91181739 G>A maps to NM_022769.3 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr15:91181739 G>A maps to NM_022769.3 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr16:81927340 C>T maps to NM_002661.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr16:81927340 C>T maps to NM_002661.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr17:66366597 G>A maps to NM_014960.3 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr17:66366597 G>A maps to NM_014960.3 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr18:13056572 C>T maps to NM_032142.3 L1328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr18:13056572 C>T maps to NM_032142.3 L1328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr18:14542736 G>A maps to ENST00000444806 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr18:14542736 G>A maps to ENST00000444806 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr19:41825479 G>A maps to NM_052848.1 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr19:41825479 G>A maps to NM_052848.1 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr2:25059787 G>A maps to NM_004036.3 Q554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr2:25059787 G>A maps to NM_004036.3 Q554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr2:47278894 G>A maps to ENST00000394850 R700R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr2:47278894 G>A maps to ENST00000394850 R700R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr2:128387388 G>A maps to ENST00000389524 S1572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr2:128387388 G>A maps to ENST00000389524 S1572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr2:220098636 C>T maps to NM_001042410.1 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr2:220098636 C>T maps to NM_001042410.1 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr20:58587739 G>A maps to NM_177980.2 A818A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr20:58587739 G>A maps to NM_177980.2 A818A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr3:112548232 T>C did not map to a codon.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr3:112548232 T>C did not map to a codon.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr3:150289838 C>T maps to NM_032025.3 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr3:150289838 C>T maps to NM_032025.3 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr4:71346527 C>T maps to NM_152291.2 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr4:71346527 C>T maps to NM_152291.2 R23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr5:113798814 C>G maps to NM_021614.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr5:113798814 C>G maps to NM_021614.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr6:31477568 C>T maps to NM_005931.3 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr6:31477568 C>T maps to NM_005931.3 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr6:108395462 T>A maps to NM_014028.3 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr6:108395462 T>A maps to NM_014028.3 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr6:129774130 A>C did not map to a codon.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr6:129774130 A>C did not map to a codon.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr7:83014714 A>T maps to NM_012431.2 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr7:83014714 A>T maps to NM_012431.2 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr7:139741626 A>G maps to NM_022750.2 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr7:139741626 A>G maps to NM_022750.2 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr9:2717792 G>A maps to NM_133497.2 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr9:2717792 G>A maps to NM_133497.2 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr9:120470944 G>A maps to NM_138554.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chr9:120470944 G>A maps to NM_138554.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chrX:107170194 C>A maps to NM_012216.3 I700I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chrX:107170194 C>A maps to NM_012216.3 I700I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chrX:114536557 C>T maps to NM_016383.3 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5431-01A-01D-1512-08 chrX:114536557 C>T maps to NM_016383.3 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:27627908 G>A maps to ENST00000319394 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:27627908 G>A maps to ENST00000319394 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:68948182 C>T maps to NM_001114120.1 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:68948182 C>T maps to NM_001114120.1 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:152882593 G>A maps to NM_005547.2 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:152882593 G>A maps to NM_005547.2 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:170941011 C>A maps to NM_001163629.1 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:170941011 C>A maps to NM_001163629.1 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:175375751 C>A maps to NM_003285.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:175375751 C>A maps to NM_003285.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:180151442 C>A maps to NM_002826.4 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:180151442 C>A maps to NM_002826.4 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:184868310 C>T did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:184868310 C>T did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:228612627 C>A maps to NM_003493.2 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:228612627 C>A maps to NM_003493.2 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:233750264 C>T maps to NM_002245.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:233750264 C>T maps to NM_002245.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:248525118 T>C maps to NM_001004696.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr1:248525118 T>C maps to NM_001004696.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr10:15700996 C>T did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr10:15700996 C>T did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr10:72020481 G>A maps to ENST00000277942 D112D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr10:72020481 G>A maps to ENST00000277942 D112D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr10:79764512 C>T maps to NM_007055.3 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr10:79764512 C>T maps to NM_007055.3 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr10:134563022 G>A maps to NM_005539.3 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr10:134563022 G>A maps to NM_005539.3 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:5730526 G>A maps to NM_006074.4 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:5730526 G>A maps to NM_006074.4 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:6231256 C>T maps to NM_173525.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:6231256 C>T maps to NM_173525.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:55890009 C>A maps to NM_001005201.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:55890009 C>A maps to NM_001005201.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:56000379 G>A maps to NM_001004746.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:56000379 G>A maps to NM_001004746.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:56000427 G>A maps to NM_001004746.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:56000427 G>A maps to NM_001004746.1 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:56086375 A>T maps to NM_001005202.1 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:56086375 A>T maps to NM_001005202.1 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:56344726 G>A maps to NM_001004741.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:56344726 G>A maps to NM_001004741.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:58949290 C>T maps to NM_015177.1 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:58949290 C>T maps to NM_015177.1 N97N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:108381349 G>A maps to NM_015065.2 G1628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr11:108381349 G>A maps to NM_015065.2 G1628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr12:7973849 C>T maps to NM_153449.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr12:7973849 C>T maps to NM_153449.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr12:11183778 C>T maps to NM_176885.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr12:11183778 C>T maps to NM_176885.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr12:40041679 G>T maps to NM_001031748.2 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr12:40041679 G>T maps to NM_001031748.2 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr12:113629588 G>A maps to NM_032848.1 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr12:113629588 G>A maps to NM_032848.1 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr14:35262043 G>A maps to NM_013448.2 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr14:35262043 G>A maps to NM_013448.2 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr14:42356803 A>T maps to NM_152447.3 K326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr14:42356803 A>T maps to NM_152447.3 K326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr14:55510853 G>A maps to NM_199421.1 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr14:55510853 G>A maps to NM_199421.1 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr14:64468756 A>G maps to NM_182914.2 G1248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr14:64468756 A>G maps to NM_182914.2 G1248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr15:24921688 C>T maps to NM_018958.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr15:24921688 C>T maps to NM_018958.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr15:25962005 G>T maps to NM_024490.3 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr15:25962005 G>T maps to NM_024490.3 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr15:49880218 C>T maps to NM_152647.2 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr15:49880218 C>T maps to NM_152647.2 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr16:71668180 G>A maps to NM_052858.3 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr16:71668180 G>A maps to NM_052858.3 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr16:76389224 C>A maps to NM_033401.3 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr16:76389224 C>A maps to NM_033401.3 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:4883213 G>T maps to NM_015099.3 S468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:4883213 G>T maps to NM_015099.3 S468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:7297015 G>A maps to NM_020360.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:7297015 G>A maps to NM_020360.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:7577017 C>A did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:7577017 C>A did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:10248870 G>A maps to NM_003802.2 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:10248870 G>A maps to NM_003802.2 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:11543608 C>T maps to NM_001372.3 N603N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:11543608 C>T maps to NM_001372.3 N603N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:15215749 G>C maps to NM_031898.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:15215749 G>C maps to NM_031898.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:39190614 G>A maps to NM_030966.1 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:39190614 G>A maps to NM_030966.1 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:72588682 C>T maps to NM_152460.2 C166C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr17:72588682 C>T maps to NM_152460.2 C166C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr18:40853628 C>T maps to NM_020783.3 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr18:40853628 C>T maps to NM_020783.3 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr19:52905280 G>A maps to NM_032423.2 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr19:52905280 G>A maps to NM_032423.2 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr19:55107221 G>A maps to NM_006863.1 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr19:55107221 G>A maps to NM_006863.1 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr19:58001540 A>C maps to NM_001098491.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr19:58001540 A>C maps to NM_001098491.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:77745755 T>G maps to NM_001134745.1 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:77745755 T>G maps to NM_001134745.1 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:109367718 G>T did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:109367718 G>T did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:179438978 G>T maps to NM_133378.4 I21392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:179438978 G>T maps to NM_133378.4 I21392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:179474459 A>G maps to NM_133378.4 I14662I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:179474459 A>G maps to NM_133378.4 I14662I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:179584097 G>A maps to NM_133378.4 R6763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:179584097 G>A maps to NM_133378.4 R6763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:179659663 G>A maps to NM_133378.4 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:179659663 G>A maps to NM_133378.4 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:220437167 G>A maps to NM_002191.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:220437167 G>A maps to NM_002191.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:225365204 C>A did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr2:225365204 C>A did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr20:17600949 C>T maps to ENST00000377813 S1191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr20:17600949 C>T maps to ENST00000377813 S1191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr22:22989483 G>C maps to ENST00000215938 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr22:22989483 G>C maps to ENST00000215938 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr22:39387521 G>C maps to ENST00000402182 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr22:39387521 G>C maps to ENST00000402182 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr22:46114313 C>T maps to NM_013236.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr22:46114313 C>T maps to NM_013236.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:28520394 G>T maps to NM_001040432.1 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:28520394 G>T maps to NM_001040432.1 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:50091778 C>T maps to NM_005777.2 N548N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:50091778 C>T maps to NM_005777.2 N548N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:73016866 G>T maps to NM_001080393.1 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:73016866 G>T maps to NM_001080393.1 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:74411123 G>T maps to NM_020872.1 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:74411123 G>T maps to NM_020872.1 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:78766928 G>A maps to NM_002941.3 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:78766928 G>A maps to NM_002941.3 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:85961534 T>G maps to NM_153184.3 L174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:85961534 T>G maps to NM_153184.3 L174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:89156986 G>C did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:89156986 G>C did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:123987645 G>A maps to NM_001024660.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:123987645 G>A maps to NM_001024660.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:193366586 G>T maps to NM_130837.2 E647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr3:193366586 G>T maps to NM_130837.2 E647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr4:5975388 T>C maps to ENST00000324058 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr4:5975388 T>C maps to ENST00000324058 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr4:7533274 G>A maps to NM_020777.2 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr4:7533274 G>A maps to NM_020777.2 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr4:115858476 G>T maps to NM_022569.1 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr4:115858476 G>T maps to NM_022569.1 I468I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr5:13859685 G>A maps to NM_001369.2 Q1609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr5:13859685 G>A maps to NM_001369.2 Q1609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr5:19839080 G>A maps to NM_004934.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr5:19839080 G>A maps to NM_004934.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr5:23527461 G>T maps to NM_020227.2 R755R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr5:23527461 G>T maps to NM_020227.2 R755R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr5:33616117 C>A maps to NM_030955.2 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr5:33616117 C>A maps to NM_030955.2 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr5:41052599 G>T maps to ENST00000296803 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr5:41052599 G>T maps to ENST00000296803 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr5:88047671 A>T did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr5:88047671 A>T did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr5:140262395 C>T maps to NM_018904.2 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr5:140262395 C>T maps to NM_018904.2 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr6:26246947 G>T maps to NM_003547.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr6:26246947 G>T maps to NM_003547.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr6:88387535 C>A maps to NM_018064.3 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr6:88387535 C>A maps to NM_018064.3 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr6:100964150 C>A maps to NM_006828.2 E1994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr6:100964150 C>A maps to NM_006828.2 E1994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr7:1040141 C>T maps to NM_032350.5 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr7:1040141 C>T maps to NM_032350.5 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr7:20403257 A>T did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr7:20403257 A>T did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr7:32598670 A>T maps to NM_015060.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr7:32598670 A>T maps to NM_015060.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr7:70255696 G>A maps to NM_015570.2 T1165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr7:70255696 G>A maps to NM_015570.2 T1165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr7:93108689 G>A maps to NM_001164737.1 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr7:93108689 G>A maps to NM_001164737.1 Q79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr7:121671534 C>T maps to NM_002851.2 V1696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr7:121671534 C>T maps to NM_002851.2 V1696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr7:143806845 C>A maps to NM_001005480.2 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr7:143806845 C>A maps to NM_001005480.2 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:2056621 G>A did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:2056621 G>A did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:48715930 G>A maps to NM_006904.6 C3285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:48715930 G>A maps to NM_006904.6 C3285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:73848741 T>C maps to NM_004770.2 Y384Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:73848741 T>C maps to NM_004770.2 Y384Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:92365164 G>T maps to NM_134266.1 G419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:92365164 G>T maps to NM_134266.1 G419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:95952350 C>T maps to NM_033285.3 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:95952350 C>T maps to NM_033285.3 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:110431466 A>T maps to ENST00000426474 T834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:110431466 A>T maps to ENST00000426474 T834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:139649039 T>G did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:139649039 T>G did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:144940191 C>G maps to NM_031308.1 T2410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:144940191 C>G maps to NM_031308.1 T2410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:144995519 G>A maps to NM_201380.2 R2960R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr8:144995519 G>A maps to NM_201380.2 R2960R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr9:103109583 G>A maps to NM_017746.3 H95H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr9:103109583 G>A maps to NM_017746.3 H95H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr9:119567938 G>A maps to ENST00000313400 Q790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr9:119567938 G>A maps to ENST00000313400 Q790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr9:139402541 C>G maps to NM_017617.3 A1125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr9:139402541 C>G maps to NM_017617.3 A1125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chrX:67938279 C>A maps to NM_001142503.2 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chrX:67938279 C>A maps to NM_001142503.2 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chrX:73962129 G>T maps to NM_001008537.2 S754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chrX:73962129 G>T maps to NM_001008537.2 S754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chrX:117783068 C>G maps to ENST00000276204 T1520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chrX:117783068 C>G maps to ENST00000276204 T1520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chrX:140995559 T>C maps to NM_005462.4 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chrX:140995559 T>C maps to NM_005462.4 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chrX:140995928 C>T maps to NM_005462.4 D913D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chrX:140995928 C>T maps to NM_005462.4 D913D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr1:21585218 G>C maps to NM_001397.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr1:21585218 G>C maps to NM_001397.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr1:180399398 T>A did not map to a codon.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr1:180399398 T>A did not map to a codon.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr1:207105857 G>A maps to NM_002644.3 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr1:207105857 G>A maps to NM_002644.3 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr10:46999983 G>T maps to NM_014696.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr10:46999983 G>T maps to NM_014696.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr12:6055398 G>A did not map to a codon.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr12:6055398 G>A did not map to a codon.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr12:7469735 C>T maps to NM_001080454.1 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr12:7469735 C>T maps to NM_001080454.1 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr12:15669883 A>T maps to NM_030667.1 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr12:15669883 A>T maps to NM_030667.1 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr12:18872483 A>G maps to ENST00000266505 C150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr12:18872483 A>G maps to ENST00000266505 C150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr12:71078045 T>A did not map to a codon.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr12:71078045 T>A did not map to a codon.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr12:105536969 T>C maps to NM_015275.1 Y653Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr12:105536969 T>C maps to NM_015275.1 Y653Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr15:89449093 G>A maps to NM_005928.2 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr15:89449093 G>A maps to NM_005928.2 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr16:10788292 C>G maps to NM_144674.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr16:10788292 C>G maps to NM_144674.1 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr16:48250114 C>T maps to NM_032583.3 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr16:48250114 C>T maps to NM_032583.3 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr17:11895777 G>A maps to NM_144680.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr17:11895777 G>A maps to NM_144680.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr17:37826488 G>A maps to NM_002686.3 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr17:37826488 G>A maps to NM_002686.3 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr17:62126508 A>T maps to NM_001433.3 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr17:62126508 A>T maps to NM_001433.3 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr18:54385257 C>T maps to NM_015285.2 R548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr18:54385257 C>T maps to NM_015285.2 R548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr19:2121211 G>A maps to ENST00000355272 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr19:2121211 G>A maps to ENST00000355272 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr19:17597587 C>T maps to NM_198580.1 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr19:17597587 C>T maps to NM_198580.1 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr19:38127000 C>G maps to NM_014898.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr19:38127000 C>G maps to NM_014898.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr19:41188692 G>A maps to NM_004756.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr19:41188692 G>A maps to NM_004756.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr19:47423171 C>T maps to NM_004491.4 Q414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr19:47423171 C>T maps to NM_004491.4 Q414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr19:48887691 C>T maps to NM_006801.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr19:48887691 C>T maps to NM_006801.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr19:51411650 G>T maps to NM_004917.3 C192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr19:51411650 G>T maps to NM_004917.3 C192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr21:45535280 G>A did not map to a codon.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr21:45535280 G>A did not map to a codon.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr3:168838895 C>A maps to NM_004991.3 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr3:168838895 C>A maps to NM_004991.3 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr4:162307171 G>A maps to NM_020116.3 Y757Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr4:162307171 G>A maps to NM_020116.3 Y757Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr5:26885872 G>A maps to NM_016279.3 Q578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr5:26885872 G>A maps to NM_016279.3 Q578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr5:131915146 A>G maps to NM_005732.3 E168E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr5:131915146 A>G maps to NM_005732.3 E168E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr5:140215593 G>T maps to NM_018910.2 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr5:140215593 G>T maps to NM_018910.2 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr5:140580972 C>T maps to NM_018931.2 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr5:140580972 C>T maps to NM_018931.2 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr6:1395021 C>T maps to NM_001452.1 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr6:1395021 C>T maps to NM_001452.1 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr6:56997883 C>T maps to NM_001031623.2 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr6:56997883 C>T maps to NM_001031623.2 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr7:1590489 G>T maps to NM_001097620.1 Y116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr7:1590489 G>T maps to NM_001097620.1 Y116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr7:98446237 G>T maps to NM_001134450.1 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr7:98446237 G>T maps to NM_001134450.1 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr7:99258196 A>G maps to NM_000777.3 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr7:99258196 A>G maps to NM_000777.3 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr7:106523580 C>T maps to NM_002649.2 L911L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr7:106523580 C>T maps to NM_002649.2 L911L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr8:59352287 G>A maps to NM_001077619.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr8:59352287 G>A maps to NM_001077619.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr8:75276508 G>A maps to NM_018972.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr8:75276508 G>A maps to NM_018972.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chrX:101092762 T>A maps to ENST00000263032 K304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chrX:101092762 T>A maps to ENST00000263032 K304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chrX:154294264 C>T maps to NM_001018025.3 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chrX:154294264 C>T maps to NM_001018025.3 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr1:99772406 C>T maps to NM_014839.4 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr1:99772406 C>T maps to NM_014839.4 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr1:152283934 C>A maps to NM_002016.1 G1143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr1:152283934 C>A maps to NM_002016.1 G1143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr1:177909816 C>T maps to NM_033127.2 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr1:177909816 C>T maps to NM_033127.2 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr1:205038983 C>T maps to NM_005076.3 D742D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr1:205038983 C>T maps to NM_005076.3 D742D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr1:248004559 C>A maps to NM_001001959.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr1:248004559 C>A maps to NM_001001959.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr10:43882507 T>C maps to NM_001098204.1 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr10:43882507 T>C maps to NM_001098204.1 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr10:122612035 G>A maps to NM_018117.11 W29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr10:122612035 G>A maps to NM_018117.11 W29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr11:62414589 G>A maps to NM_030628.1 L988L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr11:62414589 G>A maps to NM_030628.1 L988L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr12:20523042 G>A maps to NM_000921.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr12:20523042 G>A maps to NM_000921.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr12:120139471 C>T maps to ENST00000392521 V1833V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr12:120139471 C>T maps to ENST00000392521 V1833V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr12:124799004 C>T maps to ENST00000389727 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr12:124799004 C>T maps to ENST00000389727 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr14:63671682 G>C maps to NM_020663.3 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr14:63671682 G>C maps to NM_020663.3 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr14:65208841 C>T maps to ENST00000394691 S869S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr14:65208841 C>T maps to ENST00000394691 S869S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr15:28326954 C>T maps to NM_000275.2 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr15:28326954 C>T maps to NM_000275.2 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr15:65491099 G>A maps to NM_003613.3 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr15:65491099 G>A maps to NM_003613.3 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr15:79092701 G>A maps to ENST00000258883 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr15:79092701 G>A maps to ENST00000258883 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr15:79294031 G>T maps to NM_002891.4 P865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr15:79294031 G>T maps to NM_002891.4 P865P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr17:7579414 C>T maps to NM_001126112.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr17:7579414 C>T maps to NM_001126112.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr17:29162893 A>C maps to NM_024857.3 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr17:29162893 A>C maps to NM_024857.3 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr17:37369369 G>T maps to NM_198993.3 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr17:37369369 G>T maps to NM_198993.3 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr17:61958158 T>C maps to NM_002059.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr17:61958158 T>C maps to NM_002059.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr17:63898392 G>A maps to NM_145036.3 N680N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr17:63898392 G>A maps to NM_145036.3 N680N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr18:29848298 G>A maps to ENST00000269209 C722C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr18:29848298 G>A maps to ENST00000269209 C722C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr19:21365729 A>G maps to NM_133473.2 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr19:21365729 A>G maps to NM_133473.2 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr2:27804811 C>T maps to NM_032266.3 H1791H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr2:27804811 C>T maps to NM_032266.3 H1791H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr2:70901924 G>A maps to NM_001185054.1 D542D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr2:70901924 G>A maps to NM_001185054.1 D542D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr2:179309172 C>T maps to NM_003690.4 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr2:179309172 C>T maps to NM_003690.4 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr2:179430728 A>G maps to NM_133378.4 D24142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr2:179430728 A>G maps to NM_133378.4 D24142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr2:201798643 G>C maps to NM_006190.4 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr2:201798643 G>C maps to NM_006190.4 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr2:225400285 G>A maps to NM_003590.3 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr2:225400285 G>A maps to NM_003590.3 Q113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr3:47680265 T>C maps to NM_003074.3 G775G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr3:47680265 T>C maps to NM_003074.3 G775G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr3:98002138 A>G maps to NM_001005482.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr3:98002138 A>G maps to NM_001005482.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr3:173998975 C>T maps to NM_014932.2 P785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr3:173998975 C>T maps to NM_014932.2 P785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr3:194790785 C>T maps to NM_152531.4 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr3:194790785 C>T maps to NM_152531.4 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr4:134072872 C>T maps to NM_032961.1 Y526Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr4:134072872 C>T maps to NM_032961.1 Y526Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr5:40777688 C>G did not map to a codon.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr5:40777688 C>G did not map to a codon.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr5:145379826 C>G maps to NM_152550.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr5:145379826 C>G maps to NM_152550.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr6:46661853 G>T maps to NM_001010870.2 E1997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr6:46661853 G>T maps to NM_001010870.2 E1997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr7:154767471 C>T maps to NM_007349.3 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr7:154767471 C>T maps to NM_007349.3 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr8:2820153 G>A maps to NM_033225.5 F3154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr8:2820153 G>A maps to NM_033225.5 F3154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr8:133858164 A>G maps to ENST00000395386 V1018V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chr8:133858164 A>G maps to ENST00000395386 V1018V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chrX:103495253 C>T maps to NM_153448.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5435-01A-01D-1683-08 chrX:103495253 C>T maps to NM_153448.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr1:18962743 G>A maps to NM_002584.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr1:18962743 G>A maps to NM_002584.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr1:110294290 G>A maps to NM_139053.1 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr1:110294290 G>A maps to NM_139053.1 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr1:152277200 G>A maps to NM_002016.1 L3387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr1:152277200 G>A maps to NM_002016.1 L3387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr1:153906273 C>G maps to NM_014856.2 L1005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr1:153906273 C>G maps to NM_014856.2 L1005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr1:180155268 A>G maps to NM_002826.4 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr1:180155268 A>G maps to NM_002826.4 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr11:118888676 G>A maps to NM_001028.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr11:118888676 G>A maps to NM_001028.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr12:49428449 C>G did not map to a codon.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr12:49428449 C>G did not map to a codon.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr15:49059303 A>G maps to NM_001194998.1 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr15:49059303 A>G maps to NM_001194998.1 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr16:68849488 C>T maps to NM_004360.3 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr16:68849488 C>T maps to NM_004360.3 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr17:3195525 C>T maps to ENST00000397187 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr17:3195525 C>T maps to ENST00000397187 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr17:7579520 C>A maps to NM_001126112.1 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr17:7579520 C>A maps to NM_001126112.1 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr17:45291172 C>T maps to NM_002476.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr17:45291172 C>T maps to NM_002476.2 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr2:66739353 T>C maps to ENST00000407092 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr2:66739353 T>C maps to ENST00000407092 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr2:98355849 C>A maps to NM_001079.3 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr2:98355849 C>A maps to NM_001079.3 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr2:203745630 T>C maps to NM_018256.3 K408K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr2:203745630 T>C maps to NM_018256.3 K408K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr2:235951773 C>A maps to NM_014521.2 C787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr2:235951773 C>A maps to NM_014521.2 C787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr3:122645414 G>A maps to NM_001031702.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr3:122645414 G>A maps to NM_001031702.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr3:150903226 G>A maps to NM_053002.4 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr3:150903226 G>A maps to NM_053002.4 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr4:71227861 T>G maps to NM_012390.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr4:71227861 T>G maps to NM_012390.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr4:74702556 G>A maps to NM_002993.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr4:74702556 G>A maps to NM_002993.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr4:98480262 G>T maps to NM_174952.2 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr4:98480262 G>T maps to NM_174952.2 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr5:136448237 C>T maps to NM_004598.3 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr5:136448237 C>T maps to NM_004598.3 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr6:28264675 C>G maps to NM_032507.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr6:28264675 C>G maps to NM_032507.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr6:86328537 T>C maps to NM_006372.4 Q426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr6:86328537 T>C maps to NM_006372.4 Q426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr6:111912596 G>A maps to ENST00000340026 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr6:111912596 G>A maps to ENST00000340026 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr7:15601452 G>T maps to NM_001004320.1 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr7:15601452 G>T maps to NM_001004320.1 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr7:35242347 G>C maps to NM_001077653.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr7:35242347 G>C maps to NM_001077653.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr7:38431513 G>A maps to NM_001635.3 D571D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr7:38431513 G>A maps to NM_001635.3 D571D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr7:95019513 G>C maps to NM_000940.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr7:95019513 G>C maps to NM_000940.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr7:102982243 G>A maps to NM_014377.1 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr7:102982243 G>A maps to NM_014377.1 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr8:139606418 G>A maps to NM_152888.1 Q1486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr8:139606418 G>A maps to NM_152888.1 Q1486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr9:139905641 C>T maps to ENST00000355090 K2003K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr9:139905641 C>T maps to ENST00000355090 K2003K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr1:44596219 C>G maps to NM_173484.3 S321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr1:44596219 C>G maps to NM_173484.3 S321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr1:160523209 G>A maps to NM_001184879.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr1:160523209 G>A maps to NM_001184879.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr1:166818448 T>C maps to NM_017542.3 Y211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr1:166818448 T>C maps to NM_017542.3 Y211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr1:184764620 G>A maps to NM_052966.2 H759H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr1:184764620 G>A maps to NM_052966.2 H759H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr1:215847914 G>A maps to ENST00000366943 N4446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr1:215847914 G>A maps to ENST00000366943 N4446N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr10:24955939 T>A did not map to a codon.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr10:24955939 T>A did not map to a codon.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr10:49393602 A>G maps to NM_001018071.3 R784R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr10:49393602 A>G maps to NM_001018071.3 R784R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr11:56128168 C>T maps to NM_001005205.1 Y149Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr11:56128168 C>T maps to NM_001005205.1 Y149Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr11:66617738 G>T maps to NM_022172.2 V890V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr11:66617738 G>T maps to NM_022172.2 V890V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr11:113711430 G>A maps to NM_020886.2 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr11:113711430 G>A maps to NM_020886.2 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr11:124519603 G>T maps to NM_170601.3 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr11:124519603 G>T maps to NM_170601.3 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr12:15103493 C>A maps to NM_001175.4 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr12:15103493 C>A maps to NM_001175.4 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr12:49943927 G>A maps to NM_012284.1 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr12:49943927 G>A maps to NM_012284.1 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr12:53086202 A>G did not map to a codon.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr12:53086202 A>G did not map to a codon.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr12:56089325 C>T maps to ENST00000347027 T705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr12:56089325 C>T maps to ENST00000347027 T705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr12:103352675 T>C maps to NM_004316.3 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr12:103352675 T>C maps to NM_004316.3 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr12:110246112 C>A maps to NM_021625.4 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr12:110246112 C>A maps to NM_021625.4 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr16:68716357 G>T maps to NM_001793.4 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr16:68716357 G>T maps to NM_001793.4 E384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr17:10555772 G>A maps to NM_002470.2 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr17:10555772 G>A maps to NM_002470.2 Y104Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr17:67031932 C>T maps to NM_080283.3 W270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr17:67031932 C>T maps to NM_080283.3 W270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr19:9721790 T>A maps to NM_152289.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr19:9721790 T>A maps to NM_152289.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr19:14069908 G>A maps to NM_138353.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr19:14069908 G>A maps to NM_138353.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr19:18726930 G>T maps to NM_012109.2 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr19:18726930 G>T maps to NM_012109.2 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr19:35849959 C>T maps to NM_005304.3 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr19:35849959 C>T maps to NM_005304.3 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr19:42820841 C>T maps to ENST00000406159 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr19:42820841 C>T maps to ENST00000406159 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr2:3469399 G>T maps to NM_016030.5 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr2:3469399 G>T maps to NM_016030.5 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr2:21234135 G>T maps to NM_000384.2 L1868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr2:21234135 G>T maps to NM_000384.2 L1868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr2:28117397 A>T did not map to a codon.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr2:28117397 A>T did not map to a codon.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr2:125284859 A>G did not map to a codon.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr2:125284859 A>G did not map to a codon.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr22:38061757 G>T maps to ENST00000442465 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr22:38061757 G>T maps to ENST00000442465 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr22:46655439 G>A maps to NM_006071.1 T1260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr22:46655439 G>A maps to NM_006071.1 T1260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr4:6082003 C>T maps to NM_001099433.1 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr4:6082003 C>T maps to NM_001099433.1 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr5:1268651 C>T maps to NM_198253.2 A855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr5:1268651 C>T maps to NM_198253.2 A855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr5:26885960 T>C maps to NM_016279.3 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr5:26885960 T>C maps to NM_016279.3 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr5:76624876 G>T maps to NM_003719.3 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr5:76624876 G>T maps to NM_003719.3 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr6:13642753 G>A maps to NM_005493.2 D394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr6:13642753 G>A maps to NM_005493.2 D394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr7:1027133 C>G maps to NM_017781.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr7:1027133 C>G maps to NM_017781.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr7:38433622 G>T maps to NM_001635.3 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr7:38433622 G>T maps to NM_001635.3 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr7:100778861 C>T maps to NM_000602.3 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr7:100778861 C>T maps to NM_000602.3 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr8:71619347 C>G maps to NM_001011720.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr8:71619347 C>G maps to NM_001011720.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr8:73942568 A>G did not map to a codon.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr8:73942568 A>G did not map to a codon.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr9:84605870 G>A maps to NM_001001670.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr9:84605870 G>A maps to NM_001001670.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr9:139418286 C>A maps to NM_017617.3 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chr9:139418286 C>A maps to NM_017617.3 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chrX:76875968 A>G maps to NM_000489.3 H1722H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5439-01A-01D-1683-08 chrX:76875968 A>G maps to NM_000489.3 H1722H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr1:89834113 G>T maps to NM_198460.2 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr1:89834113 G>T maps to NM_198460.2 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr10:89624188 C>G did not map to a codon.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr10:89624188 C>G did not map to a codon.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr10:121339444 A>T did not map to a codon.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr10:121339444 A>T did not map to a codon.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr11:12379875 G>A maps to NM_032867.2 E646E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr11:12379875 G>A maps to NM_032867.2 E646E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr11:67044772 G>A maps to NM_001619.3 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr11:67044772 G>A maps to NM_001619.3 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr11:92714994 G>A maps to NM_005959.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr11:92714994 G>A maps to NM_005959.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr12:6691341 G>C maps to ENST00000309577 V1520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr12:6691341 G>C maps to ENST00000309577 V1520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr12:15262052 G>A maps to NM_032918.2 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr12:15262052 G>A maps to NM_032918.2 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr12:56721835 T>A maps to NM_001127460.2 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr12:56721835 T>A maps to NM_001127460.2 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr13:25451308 C>G maps to ENST00000381927 L1635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr13:25451308 C>G maps to ENST00000381927 L1635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr13:49752753 G>A maps to NM_001079673.1 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr13:49752753 G>A maps to NM_001079673.1 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr14:88945293 C>T maps to NM_007039.3 K827K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr14:88945293 C>T maps to NM_007039.3 K827K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr14:92563178 C>A maps to ENST00000359819 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr14:92563178 C>A maps to ENST00000359819 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr15:49320739 A>G maps to NM_001193489.1 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr15:49320739 A>G maps to NM_001193489.1 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr16:2164257 G>C maps to NM_001009944.2 L922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr16:2164257 G>C maps to NM_001009944.2 L922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr16:2166978 G>A maps to NM_001009944.2 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr16:2166978 G>A maps to NM_001009944.2 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr16:14312824 A>G maps to NM_014048.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr16:14312824 A>G maps to NM_014048.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr16:81971421 C>T maps to NM_002661.2 L1038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr16:81971421 C>T maps to NM_002661.2 L1038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr16:89350643 G>C maps to NM_013275.4 S769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr16:89350643 G>C maps to NM_013275.4 S769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr17:7483024 C>T maps to NM_001251.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr17:7483024 C>T maps to NM_001251.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr17:9774113 C>G maps to NM_004246.1 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr17:9774113 C>G maps to NM_004246.1 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr17:72951929 G>A maps to NM_030630.2 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr17:72951929 G>A maps to NM_030630.2 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr19:18853805 C>T maps to NM_001098482.1 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr19:18853805 C>T maps to NM_001098482.1 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr19:44738976 C>T maps to NM_182490.1 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr19:44738976 C>T maps to NM_182490.1 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr19:46215298 G>A maps to NM_001080469.1 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr19:46215298 G>A maps to NM_001080469.1 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr21:46925145 C>T maps to ENST00000359759 P1404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr21:46925145 C>T maps to ENST00000359759 P1404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr3:148791053 A>G maps to NM_003071.3 Y195Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr3:148791053 A>G maps to NM_003071.3 Y195Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr5:35705827 C>A maps to NM_024867.3 I861I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr5:35705827 C>A maps to NM_024867.3 I861I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr5:129241115 C>T maps to NM_175856.4 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr5:129241115 C>T maps to NM_175856.4 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr6:30681829 G>A maps to NM_014641.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr6:30681829 G>A maps to NM_014641.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr6:31122386 T>A maps to NM_001105564.1 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr6:31122386 T>A maps to NM_001105564.1 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr6:163510333 C>G maps to NM_152410.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr6:163510333 C>G maps to NM_152410.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr7:128407639 C>T maps to ENST00000342367 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr7:128407639 C>T maps to ENST00000342367 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr8:68092139 G>T maps to ENST00000389042 E1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr8:68092139 G>T maps to ENST00000389042 E1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr8:117668120 T>C maps to ENST00000411422 K241K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr8:117668120 T>C maps to ENST00000411422 K241K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr8:126062853 G>A maps to ENST00000377985 R722R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr8:126062853 G>A maps to ENST00000377985 R722R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr9:82333858 G>A maps to ENST00000376537 K553K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr9:82333858 G>A maps to ENST00000376537 K553K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr9:93641136 C>T maps to NM_003177.5 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr9:93641136 C>T maps to NM_003177.5 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr9:116150609 C>T maps to ENST00000277315 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr9:116150609 C>T maps to ENST00000277315 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr9:136132862 C>T maps to NM_020469.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5440-01A-01D-1512-08 chr9:136132862 C>T maps to NM_020469.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:2160688 A>T maps to NM_003036.3 K162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:2160688 A>T maps to NM_003036.3 K162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:55599817 C>T maps to NM_015306.2 R1102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:55599817 C>T maps to NM_015306.2 R1102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:78429829 C>A maps to ENST00000436586 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:78429829 C>A maps to ENST00000436586 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:103343705 C>A maps to NM_080629.2 E1776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:103343705 C>A maps to NM_080629.2 E1776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:154516994 T>A did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:154516994 T>A did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:154931793 G>A maps to NM_138300.3 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:154931793 G>A maps to NM_138300.3 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:176853474 C>A maps to ENST00000281881 E1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:176853474 C>A maps to ENST00000281881 E1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:204131244 G>T maps to NM_000537.3 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:204131244 G>T maps to NM_000537.3 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:234452394 C>T maps to NM_173508.2 Y292Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr1:234452394 C>T maps to NM_173508.2 Y292Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr10:56077051 G>T maps to NM_001142763.1 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr10:56077051 G>T maps to NM_001142763.1 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr10:68280483 C>A maps to NM_013266.2 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr10:68280483 C>A maps to NM_013266.2 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr10:85901367 C>T maps to ENST00000436406 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr10:85901367 C>T maps to ENST00000436406 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr10:102050188 C>A maps to NM_016112.2 G699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr10:102050188 C>A maps to NM_016112.2 G699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr11:5221654 C>T maps to NM_001004760.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr11:5221654 C>T maps to NM_001004760.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr11:6048724 G>A maps to NM_001001917.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr11:6048724 G>A maps to NM_001001917.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr11:51515640 C>T maps to NM_001004703.1 H120H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr11:51515640 C>T maps to NM_001004703.1 H120H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr11:88911459 A>C maps to NM_000372.4 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr11:88911459 A>C maps to NM_000372.4 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:993326 G>A maps to NM_001184985.1 A1514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:993326 G>A maps to NM_001184985.1 A1514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:7241887 C>T did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:7241887 C>T did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:8083211 C>A maps to NM_006931.2 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:8083211 C>A maps to NM_006931.2 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:10569333 C>T maps to NM_007333.2 W173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:10569333 C>T maps to NM_007333.2 W173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:21970132 C>A maps to NM_005691.2 E1294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:21970132 C>A maps to NM_005691.2 E1294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:49420594 G>A maps to NM_003482.3 L5052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:49420594 G>A maps to NM_003482.3 L5052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:52979792 G>A maps to NM_080747.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:52979792 G>A maps to NM_080747.2 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:113543659 C>A maps to NM_001193520.1 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:113543659 C>A maps to NM_001193520.1 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:129294619 T>C maps to ENST00000376744 Q293Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:129294619 T>C maps to ENST00000376744 Q293Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:129360581 C>G maps to ENST00000442111 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:129360581 C>G maps to ENST00000442111 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:130185031 G>A maps to NM_133448.2 Y97Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:130185031 G>A maps to NM_133448.2 Y97Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:133212600 T>C maps to ENST00000455752 S1899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr12:133212600 T>C maps to ENST00000455752 S1899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr13:25744107 G>T maps to NM_152704.2 Y550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr13:25744107 G>T maps to NM_152704.2 Y550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr13:58208986 G>T maps to NM_001040429.2 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr13:58208986 G>T maps to NM_001040429.2 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr13:70549882 A>G maps to NM_020866.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr13:70549882 A>G maps to NM_020866.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr13:101910913 C>T maps to NM_052867.2 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr13:101910913 C>T maps to NM_052867.2 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr14:23313039 C>T maps to NM_004995.2 D324D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr14:23313039 C>T maps to NM_004995.2 D324D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr14:24884815 C>G maps to NM_025081.2 P1287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr14:24884815 C>G maps to NM_025081.2 P1287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr14:64891612 C>T maps to NM_005956.3 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr14:64891612 C>T maps to NM_005956.3 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr14:72200506 A>G maps to NM_015556.1 V1683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr14:72200506 A>G maps to NM_015556.1 V1683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr14:75150017 G>A maps to NM_001039479.1 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr14:75150017 G>A maps to NM_001039479.1 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:23811399 G>A maps to NM_005664.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:23811399 G>A maps to NM_005664.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:23932094 C>T maps to NM_002487.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:23932094 C>T maps to NM_002487.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:31324987 G>A maps to NM_002420.4 I930I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:31324987 G>A maps to NM_002420.4 I930I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:38591586 C>T maps to NM_152594.2 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:38591586 C>T maps to NM_152594.2 R16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:48055234 A>T maps to NM_153618.1 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:48055234 A>T maps to NM_153618.1 I227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:60745948 T>A maps to NM_024611.4 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:60745948 T>A maps to NM_024611.4 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:67073770 C>T maps to NM_005585.4 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:67073770 C>T maps to NM_005585.4 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:89873427 G>A maps to NM_002693.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr15:89873427 G>A maps to NM_002693.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr16:20487095 G>T did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr16:20487095 G>T did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr16:28995108 C>T maps to NM_032038.2 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr16:28995108 C>T maps to NM_032038.2 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr16:68598393 C>T maps to NM_133458.2 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr16:68598393 C>T maps to NM_133458.2 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr16:77375633 G>C maps to NM_199355.2 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr16:77375633 G>C maps to NM_199355.2 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr17:7370090 C>T maps to NM_020899.3 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr17:7370090 C>T maps to NM_020899.3 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr17:7806007 G>A maps to NM_001005271.2 T1170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr17:7806007 G>A maps to NM_001005271.2 T1170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr17:10304006 T>C maps to NM_002472.2 E1145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr17:10304006 T>C maps to NM_002472.2 E1145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr17:27963639 T>C maps to NM_033389.2 E509E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr17:27963639 T>C maps to NM_033389.2 E509E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr17:40937376 G>T maps to NM_032387.4 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr17:40937376 G>T maps to NM_032387.4 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr17:77768667 G>T maps to NM_020649.2 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr17:77768667 G>T maps to NM_020649.2 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr18:13053022 G>T maps to NM_032142.3 T1041T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr18:13053022 G>T maps to NM_032142.3 T1041T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:1105706 C>G maps to NM_002085.3 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:1105706 C>G maps to NM_002085.3 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:15905709 C>A maps to NM_001004466.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:15905709 C>A maps to NM_001004466.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:15989673 G>A maps to NM_001082.3 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:15989673 G>A maps to NM_001082.3 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:16861003 G>A maps to ENST00000438489 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:16861003 G>A maps to ENST00000438489 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:17631871 G>A maps to NM_012088.2 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:17631871 G>A maps to NM_012088.2 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:31025859 T>C maps to NM_014717.1 T759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:31025859 T>C maps to NM_014717.1 T759T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:36381393 T>A did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:36381393 T>A did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:39760160 C>T maps to NM_172138.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:39760160 C>T maps to NM_172138.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:45872212 G>T maps to NM_000400.3 S74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:45872212 G>T maps to NM_000400.3 S74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:49684705 C>T maps to NM_017636.3 D417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:49684705 C>T maps to NM_017636.3 D417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:56703217 C>A did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:56703217 C>A did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:57176559 C>A maps to NM_001005850.1 G25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr19:57176559 C>A maps to NM_001005850.1 G25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:8871437 C>G maps to NM_020738.2 A1576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:8871437 C>G maps to NM_020738.2 A1576A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:31489392 C>T maps to NM_014600.2 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:31489392 C>T maps to NM_014600.2 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:74684870 G>C maps to ENST00000452361 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:74684870 G>C maps to ENST00000452361 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:80530248 G>T maps to NM_178839.4 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:80530248 G>T maps to NM_178839.4 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:80530449 C>G maps to NM_178839.4 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:80530449 C>G maps to NM_178839.4 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:109547446 C>A maps to ENST00000376651 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:109547446 C>A maps to ENST00000376651 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:155555406 G>A maps to NM_002239.2 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:155555406 G>A maps to NM_002239.2 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:170013896 G>A maps to NM_004525.2 D4001D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:170013896 G>A maps to NM_004525.2 D4001D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:179462733 C>A maps to NM_133378.4 E16487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:179462733 C>A maps to NM_133378.4 E16487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:196544870 G>A maps to NM_001127257.1 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:196544870 G>A maps to NM_001127257.1 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:225740755 C>A maps to NM_014689.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:225740755 C>A maps to NM_014689.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:226446801 G>A maps to NM_020864.1 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr2:226446801 G>A maps to NM_020864.1 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr20:5166472 G>A did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr20:5166472 G>A did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr20:5283102 G>T maps to NM_144773.2 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr20:5283102 G>T maps to NM_144773.2 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr20:23017172 C>A maps to NM_001052.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr20:23017172 C>A maps to NM_001052.2 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr20:31434485 G>A maps to NM_012325.2 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr20:31434485 G>A maps to NM_012325.2 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr20:31685547 C>A maps to NM_182519.2 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr20:31685547 C>A maps to NM_182519.2 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr20:37464724 C>A maps to NM_015568.2 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr20:37464724 C>A maps to NM_015568.2 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr21:47537348 G>A maps to NM_001849.3 K345K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr21:47537348 G>A maps to NM_001849.3 K345K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr22:22868459 G>A maps to NM_080740.3 Q499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr22:22868459 G>A maps to NM_080740.3 Q499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr22:37462242 G>A maps to ENST00000381792 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr22:37462242 G>A maps to ENST00000381792 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr22:37769435 G>A maps to NM_052906.3 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr22:37769435 G>A maps to NM_052906.3 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr22:39907349 C>A maps to NM_019008.4 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr22:39907349 C>A maps to NM_019008.4 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr3:39307931 A>T maps to NM_001171174.1 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr3:39307931 A>T maps to NM_001171174.1 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr3:49755533 G>A maps to NM_198722.2 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr3:49755533 G>A maps to NM_198722.2 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr3:114069726 G>T maps to NM_001164342.1 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr3:114069726 G>T maps to NM_001164342.1 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr3:164907541 G>C maps to NM_014926.2 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr3:164907541 G>C maps to NM_014926.2 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr3:173997335 C>A maps to NM_014932.2 I515I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr3:173997335 C>A maps to NM_014932.2 I515I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr3:194947465 C>T maps to NM_152531.4 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr3:194947465 C>T maps to NM_152531.4 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr4:43022368 A>T did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr4:43022368 A>T did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr4:91549259 G>T maps to NM_001145065.1 A603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr4:91549259 G>T maps to NM_001145065.1 A603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr4:162841664 C>A maps to NM_020116.3 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr4:162841664 C>A maps to NM_020116.3 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr5:39381568 G>T maps to NM_001343.2 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr5:39381568 G>T maps to NM_001343.2 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr5:139908267 C>T maps to ENST00000253810 L1913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr5:139908267 C>T maps to ENST00000253810 L1913L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr5:140763188 C>T maps to NM_018920.2 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr5:140763188 C>T maps to NM_018920.2 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr5:140868944 G>C maps to NM_018929.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr5:140868944 G>C maps to NM_018929.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:27925795 C>T maps to NM_012367.1 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:27925795 C>T maps to NM_012367.1 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:54806054 G>A maps to NM_001010872.1 K762K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:54806054 G>A maps to NM_001010872.1 K762K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:88854006 C>T maps to NM_016083.4 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:88854006 C>T maps to NM_016083.4 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:117825023 A>G maps to ENST00000338728 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:117825023 A>G maps to ENST00000338728 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:118635270 C>A maps to NM_001029858.3 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:118635270 C>A maps to NM_001029858.3 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:125614025 T>A maps to NM_016063.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:125614025 T>A maps to NM_016063.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:131946090 A>G maps to ENST00000403834 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:131946090 A>G maps to ENST00000403834 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:144779940 G>T maps to NM_007124.2 E774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:144779940 G>T maps to NM_007124.2 E774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:152623105 G>A maps to NM_182961.2 T5813T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:152623105 G>A maps to NM_182961.2 T5813T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:152757236 C>A did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr6:152757236 C>A did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:43400527 G>T maps to NM_015052.3 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:43400527 G>T maps to NM_015052.3 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:53103939 C>T maps to NM_182595.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:53103939 C>T maps to NM_182595.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:81693670 C>G did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:81693670 C>G did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:100280796 C>G maps to NM_022574.4 V750V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:100280796 C>G maps to NM_022574.4 V750V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:106507992 A>T did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:106507992 A>T did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:131128283 T>C maps to NM_013255.4 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:131128283 T>C maps to NM_013255.4 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:141719027 G>A maps to ENST00000475668 W119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:141719027 G>A maps to ENST00000475668 W119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:143028712 G>A maps to NM_000083.2 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr7:143028712 G>A maps to NM_000083.2 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr8:27668592 C>T maps to NM_018492.2 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr8:27668592 C>T maps to NM_018492.2 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr8:105105869 A>T maps to ENST00000436393 R965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr8:105105869 A>T maps to ENST00000436393 R965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr8:139620233 T>G did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr8:139620233 T>G did not map to a codon.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr8:145642056 C>A maps to NM_130849.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr8:145642056 C>A maps to NM_130849.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr9:35869981 C>G maps to NM_001004487.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr9:35869981 C>G maps to NM_001004487.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr9:71503928 G>A maps to NM_003558.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chr9:71503928 G>A maps to NM_003558.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chrX:39933956 T>A maps to NM_001123385.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chrX:39933956 T>A maps to NM_001123385.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chrX:40513655 G>A maps to NM_004229.3 N1417N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chrX:40513655 G>A maps to NM_004229.3 N1417N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chrX:70836724 G>A maps to NM_001142797.1 N246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5441-01A-01D-1512-08 chrX:70836724 G>A maps to NM_001142797.1 N246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:45218849 G>A maps to NM_006845.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:45218849 G>A maps to NM_006845.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:89582906 C>T maps to NM_004120.3 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:89582906 C>T maps to NM_004120.3 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:155686885 G>A maps to NM_004632.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:155686885 G>A maps to NM_004632.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:156897320 C>T maps to NM_144702.2 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:156897320 C>T maps to NM_144702.2 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:160183266 G>A maps to ENST00000368075 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:160183266 G>A maps to ENST00000368075 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:197404460 C>T maps to NM_201253.2 D1156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:197404460 C>T maps to NM_201253.2 D1156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:204170909 G>A maps to NM_198447.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:204170909 G>A maps to NM_198447.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:207010081 C>T maps to NM_153758.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:207010081 C>T maps to NM_153758.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:248616451 C>T maps to NM_001004136.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:248616451 C>T maps to NM_001004136.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr10:24896475 G>C maps to NM_020824.3 S879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr10:24896475 G>C maps to NM_020824.3 S879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr10:50966433 C>A did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr10:50966433 C>A did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr10:113932771 G>A maps to NM_020918.4 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr10:113932771 G>A maps to NM_020918.4 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr11:2428394 G>A maps to ENST00000452833 L1026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr11:2428394 G>A maps to ENST00000452833 L1026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr11:48347157 G>T maps to NM_001004702.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr11:48347157 G>T maps to NM_001004702.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr12:5603697 G>A maps to NM_001102654.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr12:5603697 G>A maps to NM_001102654.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr12:53647819 C>A maps to NM_001170790.1 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr12:53647819 C>A maps to NM_001170790.1 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr12:53675380 C>T maps to NM_012291.4 R864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr12:53675380 C>T maps to NM_012291.4 R864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr12:96254998 G>T maps to NM_003095.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr12:96254998 G>T maps to NM_003095.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr12:132636124 C>T maps to NM_024078.1 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr12:132636124 C>T maps to NM_024078.1 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr14:24710318 G>A maps to NM_001099274.1 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr14:24710318 G>A maps to NM_001099274.1 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr14:38678914 C>T maps to NM_001049.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr14:38678914 C>T maps to NM_001049.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr14:79423681 C>T maps to NM_004796.4 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr14:79423681 C>T maps to NM_004796.4 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr14:92949144 C>T maps to NM_153646.3 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr14:92949144 C>T maps to NM_153646.3 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr14:100192928 G>A maps to NM_006668.1 Q456Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr14:100192928 G>A maps to NM_006668.1 Q456Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr15:42734334 C>T maps to NM_022473.1 E1210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr15:42734334 C>T maps to NM_022473.1 E1210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr15:72455740 G>A maps to NM_001012642.2 C274C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr15:72455740 G>A maps to NM_001012642.2 C274C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr16:23491206 G>C maps to NM_015044.4 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr16:23491206 G>C maps to NM_015044.4 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr16:71798595 G>A maps to ENST00000423132 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr16:71798595 G>A maps to ENST00000423132 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr17:9532072 C>T maps to NM_145054.4 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr17:9532072 C>T maps to NM_145054.4 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr17:72349697 G>A maps to NM_153209.3 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr17:72349697 G>A maps to NM_153209.3 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr18:47812520 C>T maps to NM_001101654.1 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr18:47812520 C>T maps to NM_001101654.1 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr18:48331679 G>C maps to NM_001127176.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr18:48331679 G>C maps to NM_001127176.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:6828658 C>G maps to NM_005428.2 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:6828658 C>G maps to NM_005428.2 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:8606806 C>G maps to NM_012335.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:8606806 C>G maps to NM_012335.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:8616659 G>A maps to NM_012335.3 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:8616659 G>A maps to NM_012335.3 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:9204175 C>T maps to ENST00000305465 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:9204175 C>T maps to ENST00000305465 Q89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:18252810 G>A maps to NM_015016.1 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:18252810 G>A maps to NM_015016.1 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:19740867 C>T maps to NM_016573.2 E939E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:19740867 C>T maps to NM_016573.2 E939E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:55899355 C>T maps to NM_001136135.1 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:55899355 C>T maps to NM_001136135.1 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:57175432 G>A maps to NM_001005850.1 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:57175432 G>A maps to NM_001005850.1 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:58189589 G>T maps to NM_152677.2 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr19:58189589 G>T maps to NM_152677.2 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr2:1926708 C>A maps to ENST00000399161 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr2:1926708 C>A maps to ENST00000399161 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr2:36956605 G>A maps to NM_053276.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr2:36956605 G>A maps to NM_053276.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr2:48681850 C>T maps to NM_001135629.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr2:48681850 C>T maps to NM_001135629.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr2:191873690 G>A maps to NM_007315.3 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr2:191873690 G>A maps to NM_007315.3 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr2:215843707 G>A maps to NM_173076.2 I1599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr2:215843707 G>A maps to NM_173076.2 I1599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr20:40065913 C>T maps to NM_032221.3 T1356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr20:40065913 C>T maps to NM_032221.3 T1356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr20:43030050 C>T maps to ENST00000338692 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr20:43030050 C>T maps to ENST00000338692 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr20:56073692 G>A maps to ENST00000423479 V635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr20:56073692 G>A maps to ENST00000423479 V635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr21:15525003 G>A maps to NM_198996.2 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr21:15525003 G>A maps to NM_198996.2 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr21:34931546 G>A maps to NM_138927.1 Q2111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr21:34931546 G>A maps to NM_138927.1 Q2111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr22:30691790 C>T maps to ENST00000403477 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr22:30691790 C>T maps to ENST00000403477 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr22:42461762 C>T maps to NM_000262.2 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr22:42461762 C>T maps to NM_000262.2 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr22:47071406 G>A maps to NM_015124.2 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr22:47071406 G>A maps to NM_015124.2 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr3:43388881 C>G maps to NM_017719.4 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr3:43388881 C>G maps to NM_017719.4 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr3:44951843 G>A maps to NM_003241.3 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr3:44951843 G>A maps to NM_003241.3 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr3:51752121 G>A maps to NM_000839.3 S871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr3:51752121 G>A maps to NM_000839.3 S871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr3:58155431 C>T maps to NM_001164317.1 D2542D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr3:58155431 C>T maps to NM_001164317.1 D2542D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr3:69088018 G>A maps to NM_007114.2 Q657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr3:69088018 G>A maps to NM_007114.2 Q657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr3:73432818 C>T maps to NM_015009.1 E966E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr3:73432818 C>T maps to NM_015009.1 E966E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr3:184043059 C>T maps to NM_001194947.1 R961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr3:184043059 C>T maps to NM_001194947.1 R961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr4:88231423 C>T maps to NM_178135.3 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr4:88231423 C>T maps to NM_178135.3 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr4:164271505 C>T maps to NM_006174.2 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr4:164271505 C>T maps to NM_006174.2 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr5:36181998 G>T maps to NM_005983.2 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr5:36181998 G>T maps to NM_005983.2 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr5:140209499 G>A maps to NM_018909.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr5:140209499 G>A maps to NM_018909.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr5:140626471 G>A maps to NM_018935.2 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr5:140626471 G>A maps to NM_018935.2 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr5:140720676 G>A maps to NM_018915.2 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr5:140720676 G>A maps to NM_018915.2 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr5:176072439 C>G maps to NM_001099408.1 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr5:176072439 C>G maps to NM_001099408.1 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr6:5368980 C>T maps to NM_006567.3 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr6:5368980 C>T maps to NM_006567.3 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr6:38891904 G>A maps to ENST00000327475 L3631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr6:38891904 G>A maps to ENST00000327475 L3631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr6:152456261 G>A maps to NM_182961.2 Q8589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr6:152456261 G>A maps to NM_182961.2 Q8589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:18806739 C>T maps to NM_178425.2 Q726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:18806739 C>T maps to NM_178425.2 Q726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:29132251 G>T maps to NM_031311.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:29132251 G>T maps to NM_031311.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:30639565 C>T maps to NM_002047.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:30639565 C>T maps to NM_002047.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:71252798 C>G maps to NM_031468.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:71252798 C>G maps to NM_031468.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:78131060 C>T maps to NM_012301.3 E266E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:78131060 C>T maps to NM_012301.3 E266E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:80546040 C>T maps to NM_006379.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:80546040 C>T maps to NM_006379.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:100859191 C>G maps to NM_001084.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:100859191 C>G maps to NM_001084.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:102996210 C>G maps to NM_002803.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:102996210 C>G maps to NM_002803.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:154595623 C>T maps to NM_130797.2 D486D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr7:154595623 C>T maps to NM_130797.2 D486D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr8:110401305 A>T did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr8:110401305 A>T did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr9:34107476 G>C maps to NM_015397.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr9:34107476 G>C maps to NM_015397.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr9:97082864 G>A maps to NM_017561.1 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr9:97082864 G>A maps to NM_017561.1 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr9:125921432 G>A maps to NM_018387.4 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr9:125921432 G>A maps to NM_018387.4 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chrX:19702075 G>A maps to NM_031892.2 N197N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chrX:19702075 G>A maps to NM_031892.2 N197N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chrX:53573554 T>A did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chrX:53573554 T>A did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chrX:83361413 G>A maps to NM_014496.4 R442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chrX:83361413 G>A maps to NM_014496.4 R442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chrX:138840004 G>A maps to NM_173694.4 Q891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chrX:138840004 G>A maps to NM_173694.4 Q891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chrX:144904854 G>A maps to NM_001144010.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chrX:144904854 G>A maps to NM_001144010.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr1:43777408 G>A maps to NM_005424.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr1:43777408 G>A maps to NM_005424.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr10:27702648 C>T maps to NM_001034842.3 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr10:27702648 C>T maps to NM_001034842.3 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr11:4944866 C>A maps to NM_001005237.1 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr11:4944866 C>A maps to NM_001005237.1 E235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr11:60531292 G>T maps to NM_001098835.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr11:60531292 G>T maps to NM_001098835.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr11:85420459 A>G maps to ENST00000359152 Y1484Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr11:85420459 A>G maps to ENST00000359152 Y1484Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr11:118263535 G>A maps to NM_004788.2 L1007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr11:118263535 G>A maps to NM_004788.2 L1007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr12:52710275 G>A maps to NM_002282.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr12:52710275 G>A maps to NM_002282.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr12:122975113 C>T maps to NM_017612.2 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr12:122975113 C>T maps to NM_017612.2 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr15:43821896 C>T maps to ENST00000382031 L2933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr15:43821896 C>T maps to ENST00000382031 L2933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr17:1704288 C>T maps to NM_052928.2 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr17:1704288 C>T maps to NM_052928.2 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr17:11778324 C>T maps to NM_001372.3 D3434D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr17:11778324 C>T maps to NM_001372.3 D3434D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr17:77769024 C>T maps to NM_020649.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr17:77769024 C>T maps to NM_020649.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr18:47110035 G>A maps to NM_006033.2 W423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr18:47110035 G>A maps to NM_006033.2 W423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr19:53854764 C>A maps to NM_138374.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr19:53854764 C>A maps to NM_138374.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr2:220412471 C>T maps to NM_001005209.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr2:220412471 C>T maps to NM_001005209.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr20:2297757 C>T maps to NM_003245.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr20:2297757 C>T maps to NM_003245.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr3:108773722 G>A maps to NM_014429.3 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr3:108773722 G>A maps to NM_014429.3 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr4:100062704 G>T maps to ENST00000505590 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr4:100062704 G>T maps to ENST00000505590 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr5:878567 C>T maps to NM_001009877.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr5:878567 C>T maps to NM_001009877.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr5:33549374 G>A maps to NM_030955.2 P1413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr5:33549374 G>A maps to NM_030955.2 P1413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr5:34824124 C>T maps to NM_001145521.1 N726N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr5:34824124 C>T maps to NM_001145521.1 N726N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr6:137527278 G>A maps to NM_000416.2 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr6:137527278 G>A maps to NM_000416.2 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr8:21973914 G>A maps to NM_005144.4 S1135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr8:21973914 G>A maps to NM_005144.4 S1135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr8:103664556 C>T maps to NM_005655.2 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr8:103664556 C>T maps to NM_005655.2 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr9:140058118 C>G maps to ENST00000371546 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chr9:140058118 C>G maps to ENST00000371546 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chrX:101857875 T>G maps to NM_022838.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5443-01A-01D-1512-08 chrX:101857875 T>G maps to NM_022838.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr1:1455560 G>A maps to NM_018188.3 E233E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr1:1455560 G>A maps to NM_018188.3 E233E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr1:7737773 C>T maps to NM_015215.2 H965H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr1:7737773 C>T maps to NM_015215.2 H965H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr1:40961661 C>T maps to NM_198494.2 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr1:40961661 C>T maps to NM_198494.2 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr1:53736920 G>C maps to NM_004631.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr1:53736920 G>C maps to NM_004631.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr1:75622624 T>G maps to NM_001001933.1 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr1:75622624 T>G maps to NM_001001933.1 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr1:145538041 C>A maps to NM_003637.3 V907V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr1:145538041 C>A maps to NM_003637.3 V907V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr1:202569512 G>C maps to NM_177402.4 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr1:202569512 G>C maps to NM_177402.4 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr10:71902545 G>C maps to NM_173555.2 S454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr10:71902545 G>C maps to NM_173555.2 S454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr11:46400011 G>T maps to NM_001105540.1 E982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr11:46400011 G>T maps to NM_001105540.1 E982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr11:64698015 G>A maps to NM_006244.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr11:64698015 G>A maps to NM_006244.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr11:73067755 C>G maps to NM_014786.3 L1281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr11:73067755 C>G maps to NM_014786.3 L1281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr11:133789938 G>A maps to NM_014987.1 G1227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr11:133789938 G>A maps to NM_014987.1 G1227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr12:675229 G>A maps to NM_016533.4 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr12:675229 G>A maps to NM_016533.4 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr12:122622099 C>G maps to NM_014938.3 S706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr12:122622099 C>G maps to NM_014938.3 S706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr13:111558411 G>A maps to NM_017664.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr13:111558411 G>A maps to NM_017664.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr14:24711352 C>T maps to NM_001099274.1 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr14:24711352 C>T maps to NM_001099274.1 K62K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr14:70418889 C>G maps to NM_001034852.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr14:70418889 C>G maps to NM_001034852.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr14:73448573 G>A maps to NM_021260.2 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr14:73448573 G>A maps to NM_021260.2 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr14:74523882 C>T maps to NM_025057.2 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr14:74523882 C>T maps to NM_025057.2 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr15:73581579 G>A did not map to a codon.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr15:73581579 G>A did not map to a codon.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr16:31151713 G>A maps to NM_173502.3 S730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr16:31151713 G>A maps to NM_173502.3 S730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr16:31228220 C>T maps to NM_152901.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr16:31228220 C>T maps to NM_152901.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr16:50667325 C>A maps to NM_033119.3 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr16:50667325 C>A maps to NM_033119.3 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr17:7734556 C>A maps to NM_020877.2 T4128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr17:7734556 C>A maps to NM_020877.2 T4128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr17:10248843 G>T maps to NM_003802.2 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr17:10248843 G>T maps to NM_003802.2 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr17:79517286 G>T maps to NM_025161.5 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr17:79517286 G>T maps to NM_025161.5 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr17:79612250 G>A maps to NM_031945.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr17:79612250 G>A maps to NM_031945.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr19:5047506 C>T maps to NM_015015.2 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr19:5047506 C>T maps to NM_015015.2 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr19:52506949 C>T maps to ENST00000354939 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr19:52506949 C>T maps to ENST00000354939 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr2:86433352 C>T maps to NM_016622.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr2:86433352 C>T maps to NM_016622.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr2:106498120 G>A maps to NM_001004720.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr2:106498120 G>A maps to NM_001004720.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr2:242407682 C>T maps to NM_014808.2 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr2:242407682 C>T maps to NM_014808.2 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr20:35443717 G>C maps to NM_080627.2 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr20:35443717 G>C maps to NM_080627.2 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr3:30729874 G>A did not map to a codon.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr3:30729874 G>A did not map to a codon.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr3:141231005 T>A maps to ENST00000452898 C45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr3:141231005 T>A maps to ENST00000452898 C45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr3:151166370 C>T maps to NM_178822.4 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr3:151166370 C>T maps to NM_178822.4 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr4:82056395 T>A maps to NM_006259.1 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr4:82056395 T>A maps to NM_006259.1 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr4:165891360 C>T did not map to a codon.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr4:165891360 C>T did not map to a codon.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr5:140531979 G>A maps to NM_018939.2 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr5:140531979 G>A maps to NM_018939.2 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr5:140553834 C>T maps to NM_018940.2 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr5:140553834 C>T maps to NM_018940.2 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr5:177036572 G>A maps to NM_007255.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr5:177036572 G>A maps to NM_007255.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr6:32020543 G>A maps to ENST00000375244 T3006T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr6:32020543 G>A maps to ENST00000375244 T3006T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr6:69684691 G>T maps to NM_001704.2 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr6:69684691 G>T maps to NM_001704.2 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr6:125569433 G>A maps to NM_003287.2 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr6:125569433 G>A maps to NM_003287.2 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr7:29111496 G>A maps to NM_031311.3 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr7:29111496 G>A maps to NM_031311.3 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr7:75192563 C>T maps to NM_005338.4 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr7:75192563 C>T maps to NM_005338.4 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr7:95224334 C>T maps to NM_002612.3 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr7:95224334 C>T maps to NM_002612.3 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr7:151859793 G>C maps to ENST00000355193 S3623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr7:151859793 G>C maps to ENST00000355193 S3623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr8:103291307 G>A maps to NM_015902.4 L2044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr8:103291307 G>A maps to NM_015902.4 L2044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr8:104417025 G>A maps to NM_030780.3 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr8:104417025 G>A maps to NM_030780.3 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr8:142228640 G>A maps to NM_001080431.1 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr8:142228640 G>A maps to NM_001080431.1 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr9:127289142 G>A maps to NM_033334.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr9:127289142 G>A maps to NM_033334.2 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr9:135462893 C>T maps to NM_020064.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr9:135462893 C>T maps to NM_020064.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr9:136671216 G>A maps to NM_001134398.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr9:136671216 G>A maps to NM_001134398.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr9:139701234 C>T maps to NM_001039374.4 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr9:139701234 C>T maps to NM_001039374.4 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chrX:22095597 G>A maps to NM_000444.4 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chrX:22095597 G>A maps to NM_000444.4 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr1:19653875 C>T maps to NM_017765.2 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr1:19653875 C>T maps to NM_017765.2 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr1:156926232 C>T maps to NM_198236.1 P550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr1:156926232 C>T maps to NM_198236.1 P550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr10:63661488 G>A maps to NM_032199.2 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr10:63661488 G>A maps to NM_032199.2 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr11:8728694 C>T maps to NM_005418.3 S836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr11:8728694 C>T maps to NM_005418.3 S836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr11:71717270 C>T maps to ENST00000393695 S1840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr11:71717270 C>T maps to ENST00000393695 S1840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr11:129827742 G>A maps to NM_020228.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr11:129827742 G>A maps to NM_020228.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr12:40715963 A>T maps to NM_198578.3 T1766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr12:40715963 A>T maps to NM_198578.3 T1766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr12:56091492 G>A maps to ENST00000347027 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr12:56091492 G>A maps to ENST00000347027 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr12:122369653 C>T maps to NM_144668.4 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr12:122369653 C>T maps to NM_144668.4 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr13:72440351 G>A maps to ENST00000359684 Q186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr13:72440351 G>A maps to ENST00000359684 Q186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr14:20612329 T>C maps to NM_001004724.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr14:20612329 T>C maps to NM_001004724.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr17:2867250 G>C maps to NM_015085.4 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr17:2867250 G>C maps to NM_015085.4 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr17:19605987 C>G did not map to a codon.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr17:19605987 C>G did not map to a codon.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr18:9257170 A>G maps to NM_015208.3 R1302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr18:9257170 A>G maps to NM_015208.3 R1302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr19:7916348 C>T maps to NM_001159944.1 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr19:7916348 C>T maps to NM_001159944.1 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr2:172951394 G>A maps to NM_178120.4 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr2:172951394 G>A maps to NM_178120.4 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr2:202131497 C>T maps to NM_001080125.1 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr2:202131497 C>T maps to NM_001080125.1 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr2:240969561 G>T maps to NM_001005853.1 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr2:240969561 G>T maps to NM_001005853.1 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr21:46011579 G>T maps to NM_198688.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr21:46011579 G>T maps to NM_198688.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr3:86114797 C>T maps to NM_153184.3 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr3:86114797 C>T maps to NM_153184.3 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr4:47898590 G>A maps to NM_152995.4 I426I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr4:47898590 G>A maps to NM_152995.4 I426I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr4:70156430 T>A maps to NM_053039.1 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr4:70156430 T>A maps to NM_053039.1 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr4:187524849 G>C maps to ENST00000260147 Y3613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr4:187524849 G>C maps to ENST00000260147 Y3613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr5:160063200 G>T maps to NM_025153.2 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr5:160063200 G>T maps to NM_025153.2 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr6:122777666 T>C maps to NM_020755.2 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr6:122777666 T>C maps to NM_020755.2 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr7:48146982 C>G maps to NM_003364.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr7:48146982 C>G maps to NM_003364.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr7:100457854 G>A did not map to a codon.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr7:100457854 G>A did not map to a codon.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr7:100859996 C>T maps to NM_001084.4 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr7:100859996 C>T maps to NM_001084.4 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr8:21986632 C>T maps to NM_005144.4 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr8:21986632 C>T maps to NM_005144.4 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr8:145150851 G>C maps to NM_001916.3 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr8:145150851 G>C maps to NM_001916.3 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr9:107564418 A>C maps to NM_005502.3 G1538G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr9:107564418 A>C maps to NM_005502.3 G1538G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr9:137716558 C>T maps to NM_000093.3 Y1604Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr9:137716558 C>T maps to NM_000093.3 Y1604Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chrX:68381830 A>C maps to NM_145119.3 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chrX:68381830 A>C maps to NM_145119.3 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chrX:107979061 G>A maps to NM_003604.2 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chrX:107979061 G>A maps to NM_003604.2 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chrX:117775196 G>T maps to ENST00000276204 E1397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chrX:117775196 G>T maps to ENST00000276204 E1397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr9:127652666 C>A did not map to a codon.
Sequencing variant TCGA-CV-5966-01A-11D-1683-08 chr9:127652666 C>A did not map to a codon.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr1:8390836 C>T maps to ENST00000377479 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr1:8390836 C>T maps to ENST00000377479 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr1:43778830 C>T maps to NM_005424.2 H651H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr1:43778830 C>T maps to NM_005424.2 H651H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr1:44303968 G>A maps to NM_174963.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr1:44303968 G>A maps to NM_174963.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr1:54610232 C>G maps to NM_201546.2 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr1:54610232 C>G maps to NM_201546.2 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr1:119964588 G>A maps to NM_000198.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr1:119964588 G>A maps to NM_000198.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr1:155160216 C>T maps to ENST00000425082 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr1:155160216 C>T maps to ENST00000425082 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr10:48414495 C>T maps to NM_016204.1 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr10:48414495 C>T maps to NM_016204.1 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr10:106075038 G>A maps to NM_033397.2 C257C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr10:106075038 G>A maps to NM_033397.2 C257C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr11:14490303 G>A maps to NM_001144061.1 Q690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr11:14490303 G>A maps to NM_001144061.1 Q690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr11:55135811 C>A maps to NM_001005275.1 Y151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr11:55135811 C>A maps to NM_001005275.1 Y151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr11:64678742 C>T maps to ENST00000421419 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr11:64678742 C>T maps to ENST00000421419 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr11:68131337 G>A maps to NM_002335.2 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr11:68131337 G>A maps to NM_002335.2 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr11:75299191 G>A maps to NM_033063.1 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr11:75299191 G>A maps to NM_033063.1 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr12:6690554 C>G did not map to a codon.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr12:6690554 C>G did not map to a codon.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr12:9349218 C>T maps to NM_002864.2 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr12:9349218 C>T maps to NM_002864.2 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr12:27841991 G>A maps to NM_003622.3 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr12:27841991 G>A maps to NM_003622.3 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr12:50616055 G>A maps to NM_001113546.1 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr12:50616055 G>A maps to NM_001113546.1 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr12:53227933 C>T maps to NM_175834.2 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr12:53227933 C>T maps to NM_175834.2 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr12:78531083 T>G maps to NM_014903.4 S1523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr12:78531083 T>G maps to NM_014903.4 S1523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr12:120636692 G>A maps to NM_053275.3 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr12:120636692 G>A maps to NM_053275.3 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr14:24546187 G>A maps to NM_006032.2 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr14:24546187 G>A maps to NM_006032.2 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr14:50262629 G>C maps to NM_004713.3 S833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr14:50262629 G>C maps to NM_004713.3 S833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr15:31295038 G>A maps to NM_002420.4 S1266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr15:31295038 G>A maps to NM_002420.4 S1266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr16:28883643 C>T maps to NM_001145795.1 H549H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr16:28883643 C>T maps to NM_001145795.1 H549H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr16:65032723 A>G maps to NM_001797.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr16:65032723 A>G maps to NM_001797.2 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr16:86612541 G>A maps to NM_005250.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr16:86612541 G>A maps to NM_005250.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr16:90016034 G>A maps to NM_207514.1 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr16:90016034 G>A maps to NM_207514.1 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr17:78938108 G>A maps to NM_020761.2 S1329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr17:78938108 G>A maps to NM_020761.2 S1329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr18:908271 C>G maps to NM_001117.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr18:908271 C>G maps to NM_001117.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr18:42529989 G>T maps to NM_015559.2 G229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr18:42529989 G>T maps to NM_015559.2 G229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr18:52571633 G>A maps to NM_025214.2 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr18:52571633 G>A maps to NM_025214.2 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr19:1581179 G>C maps to NM_003926.5 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr19:1581179 G>C maps to NM_003926.5 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr19:6670017 G>A maps to NM_003807.3 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr19:6670017 G>A maps to NM_003807.3 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr19:10610148 G>A maps to NM_203500.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr19:10610148 G>A maps to NM_203500.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr19:19372351 G>A maps to NM_023002.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr19:19372351 G>A maps to NM_023002.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr19:42260721 C>T maps to NM_002483.4 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr19:42260721 C>T maps to NM_002483.4 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr19:46832528 C>G maps to NM_152795.2 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr19:46832528 C>G maps to NM_152795.2 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr19:56953258 G>T maps to ENST00000342634 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr19:56953258 G>T maps to ENST00000342634 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:25978929 G>A maps to NM_018263.4 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:25978929 G>A maps to NM_018263.4 F331F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:27015012 C>T maps to NM_001809.3 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:27015012 C>T maps to NM_001809.3 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:40656664 C>G maps to NM_021097.2 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:40656664 C>G maps to NM_021097.2 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:80530152 C>G maps to NM_178839.4 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:80530152 C>G maps to NM_178839.4 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:80530266 G>A maps to NM_178839.4 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:80530266 G>A maps to NM_178839.4 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:170101320 G>A maps to NM_004525.2 H1104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:170101320 G>A maps to NM_004525.2 H1104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:238785962 C>A maps to NM_005855.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:238785962 C>A maps to NM_005855.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:239003068 C>T maps to NM_016510.4 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:239003068 C>T maps to NM_016510.4 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:241987825 C>T maps to NM_001080437.1 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr2:241987825 C>T maps to NM_001080437.1 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr20:31813053 G>T did not map to a codon.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr20:31813053 G>T did not map to a codon.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr20:55777624 G>A maps to NM_001719.2 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr20:55777624 G>A maps to NM_001719.2 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr21:41416161 C>T maps to NM_001389.3 A1742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr21:41416161 C>T maps to NM_001389.3 A1742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr21:42861455 G>A maps to NM_001135099.1 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr21:42861455 G>A maps to NM_001135099.1 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr22:29139935 C>T maps to NM_172002.3 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr22:29139935 C>T maps to NM_172002.3 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr22:44079706 C>A maps to NM_022785.3 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr22:44079706 C>A maps to NM_022785.3 E391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr3:8787387 C>T maps to NM_001234.3 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr3:8787387 C>T maps to NM_001234.3 F97F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr3:150377924 C>T maps to NM_152394.3 E582E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr3:150377924 C>T maps to NM_152394.3 E582E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr4:5961119 C>T maps to ENST00000324058 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr4:5961119 C>T maps to ENST00000324058 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr5:10407239 G>A maps to NM_005885.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr5:10407239 G>A maps to NM_005885.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr5:36686247 G>A maps to NM_004172.4 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr5:36686247 G>A maps to NM_004172.4 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr5:78338268 G>A maps to NM_013391.2 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr5:78338268 G>A maps to NM_013391.2 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr5:140769022 C>T maps to NM_003736.2 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr5:140769022 C>T maps to NM_003736.2 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr6:29556071 T>C maps to NM_007160.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr6:29556071 T>C maps to NM_007160.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr6:34499520 C>T maps to NM_020804.3 Y394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr6:34499520 C>T maps to NM_020804.3 Y394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr6:35260715 G>A maps to NM_003427.3 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr6:35260715 G>A maps to NM_003427.3 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr6:88126411 G>A maps to NM_001031743.2 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr6:88126411 G>A maps to NM_001031743.2 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr7:4272923 G>A maps to NM_152744.3 P1955P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr7:4272923 G>A maps to NM_152744.3 P1955P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr7:87476267 G>A maps to NM_018843.3 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr7:87476267 G>A maps to NM_018843.3 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr7:92136440 C>T did not map to a codon.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr7:92136440 C>T did not map to a codon.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr7:151261268 C>T maps to NM_016203.3 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr7:151261268 C>T maps to NM_016203.3 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr8:48798672 C>T maps to NM_006904.6 A1535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr8:48798672 C>T maps to NM_006904.6 A1535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr9:137779203 G>A maps to NM_004108.2 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chr9:137779203 G>A maps to NM_004108.2 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chrX:147924494 G>A maps to NM_002025.3 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5970-01A-11D-1683-08 chrX:147924494 G>A maps to NM_002025.3 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr1:196918741 C>T maps to ENST00000367421 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr1:196918741 C>T maps to ENST00000367421 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr10:102056007 G>C maps to NM_016112.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr10:102056007 G>C maps to NM_016112.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr10:104415876 G>A maps to NM_030912.2 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr10:104415876 G>A maps to NM_030912.2 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr14:64746774 G>A maps to NM_001437.2 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr14:64746774 G>A maps to NM_001437.2 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr18:33283588 C>G maps to NM_020474.3 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr18:33283588 C>G maps to NM_020474.3 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr19:46444041 G>A maps to NM_002516.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr19:46444041 G>A maps to NM_002516.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr2:24046266 G>A maps to NM_017552.1 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr2:24046266 G>A maps to NM_017552.1 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr2:27804892 G>A maps to NM_032266.3 L1818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr2:27804892 G>A maps to NM_032266.3 L1818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr22:39387497 G>A maps to ENST00000402182 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr22:39387497 G>A maps to ENST00000402182 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr22:40283600 G>C maps to NM_152512.3 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr22:40283600 G>C maps to NM_152512.3 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr3:88199219 C>G maps to NM_173824.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr3:88199219 C>G maps to NM_173824.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr5:71492943 G>A maps to NM_005909.3 S1254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr5:71492943 G>A maps to NM_005909.3 S1254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr7:141490604 C>T maps to NM_018980.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5971-01A-11D-1683-08 chr7:141490604 C>T maps to NM_018980.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr1:45292685 G>T maps to NM_003738.4 T861T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr1:45292685 G>T maps to NM_003738.4 T861T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr1:150923167 A>G maps to NM_001145415.1 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr1:150923167 A>G maps to NM_001145415.1 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr1:207504537 G>A maps to NM_001114752.1 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr1:207504537 G>A maps to NM_001114752.1 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr11:35641068 C>T maps to NM_014344.3 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr11:35641068 C>T maps to NM_014344.3 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr11:59860934 C>T maps to NM_000139.4 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr11:59860934 C>T maps to NM_000139.4 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr12:49522571 G>A maps to NM_006082.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr12:49522571 G>A maps to NM_006082.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr12:78400844 C>A maps to NM_014903.4 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr12:78400844 C>A maps to NM_014903.4 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr14:44975347 C>T maps to NM_032135.3 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr14:44975347 C>T maps to NM_032135.3 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr14:77926054 G>A maps to NM_012111.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr14:77926054 G>A maps to NM_012111.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr16:71025262 T>C maps to NM_032821.2 E1274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr16:71025262 T>C maps to NM_032821.2 E1274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr17:56536135 C>T maps to NM_001080439.1 K571K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr17:56536135 C>T maps to NM_001080439.1 K571K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr19:19043824 G>A maps to NM_004838.3 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr19:19043824 G>A maps to NM_004838.3 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr19:53453767 A>T maps to NM_001031665.1 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr19:53453767 A>T maps to NM_001031665.1 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr2:99013495 G>A maps to NM_001298.2 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr2:99013495 G>A maps to NM_001298.2 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr2:109964266 C>T maps to NM_001099289.1 H237H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr2:109964266 C>T maps to NM_001099289.1 H237H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr2:220164843 G>A maps to NM_002846.3 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr2:220164843 G>A maps to NM_002846.3 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr22:30803468 C>T maps to NM_012429.2 Y100Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr22:30803468 C>T maps to NM_012429.2 Y100Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr3:47912431 C>T maps to ENST00000426837 S2055S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr3:47912431 C>T maps to ENST00000426837 S2055S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr3:121207696 G>A maps to ENST00000393672 Q1497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr3:121207696 G>A maps to ENST00000393672 Q1497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr3:135722253 A>T maps to NM_002718.4 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr3:135722253 A>T maps to NM_002718.4 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr6:35479473 G>A maps to NM_003322.3 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr6:35479473 G>A maps to NM_003322.3 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr7:13935628 T>C maps to NM_004956.4 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr7:13935628 T>C maps to NM_004956.4 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr7:150772825 G>A maps to NM_003040.3 P1145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr7:150772825 G>A maps to NM_003040.3 P1145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr9:20944733 C>T maps to NM_017794.3 H1172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr9:20944733 C>T maps to NM_017794.3 H1172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr9:79635499 C>T maps to NM_001013735.1 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr9:79635499 C>T maps to NM_001013735.1 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr9:131678562 C>T maps to NM_001127244.1 S782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr9:131678562 C>T maps to NM_001127244.1 S782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr9:139393695 G>A maps to NM_017617.3 R1984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5973-01A-11D-1683-08 chr9:139393695 G>A maps to NM_017617.3 R1984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr1:14106923 A>G maps to NM_012231.4 V878V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr1:14106923 A>G maps to NM_012231.4 V878V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr1:27682580 G>C maps to NM_004672.3 S1216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr1:27682580 G>C maps to NM_004672.3 S1216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr1:38227605 G>A maps to NM_001099439.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr1:38227605 G>A maps to NM_001099439.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr1:110022064 G>C maps to NM_001040709.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr1:110022064 G>C maps to NM_001040709.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr1:113240919 C>T maps to NM_020963.3 I776I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr1:113240919 C>T maps to NM_020963.3 I776I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr1:181701837 C>T maps to ENST00000357570 T872T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr1:181701837 C>T maps to ENST00000357570 T872T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr11:65123650 G>A maps to NM_145719.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr11:65123650 G>A maps to NM_145719.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr12:46244615 C>T maps to NM_152641.2 Q904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr12:46244615 C>T maps to NM_152641.2 Q904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr13:31891810 G>A maps to NM_194318.3 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr13:31891810 G>A maps to NM_194318.3 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr14:31598316 A>C maps to NM_015382.2 A1420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr14:31598316 A>C maps to NM_015382.2 A1420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr14:44974981 G>A maps to NM_032135.3 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr14:44974981 G>A maps to NM_032135.3 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr14:50792425 A>G maps to NM_001003803.2 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr14:50792425 A>G maps to NM_001003803.2 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr15:81592384 G>A maps to NM_172217.3 S906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr15:81592384 G>A maps to NM_172217.3 S906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr16:2983756 C>T maps to ENST00000399667 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr16:2983756 C>T maps to ENST00000399667 F430F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr19:5699114 G>A maps to NM_004793.2 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr19:5699114 G>A maps to NM_004793.2 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr19:18649083 G>A maps to NM_012181.3 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr19:18649083 G>A maps to NM_012181.3 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr2:45233323 C>T maps to NM_016932.4 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr2:45233323 C>T maps to NM_016932.4 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr2:136546022 G>A maps to NM_002299.2 Y1885Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr2:136546022 G>A maps to NM_002299.2 Y1885Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr20:47991217 G>A maps to NM_004975.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr20:47991217 G>A maps to NM_004975.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr4:46930430 G>A maps to NM_000809.2 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr4:46930430 G>A maps to NM_000809.2 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr6:4935983 G>A maps to ENST00000328908 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr6:4935983 G>A maps to ENST00000328908 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr6:10874806 G>A maps to NM_004752.3 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr6:10874806 G>A maps to NM_004752.3 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr6:29910348 C>T maps to ENST00000376806 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr6:29910348 C>T maps to ENST00000376806 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr6:31778483 G>A maps to NM_005527.3 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr6:31778483 G>A maps to NM_005527.3 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr6:110423256 T>G maps to NM_003931.2 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr6:110423256 T>G maps to NM_003931.2 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr7:37264523 G>A maps to NM_014800.9 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr7:37264523 G>A maps to NM_014800.9 Q221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr8:144944532 C>T maps to NM_031308.1 L963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr8:144944532 C>T maps to NM_031308.1 L963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr9:99522149 G>C maps to NM_014930.1 S321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr9:99522149 G>C maps to NM_014930.1 S321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chrX:35993983 C>A maps to NM_152632.3 P889P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chrX:35993983 C>A maps to NM_152632.3 P889P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr1:75072309 G>A maps to NM_001002912.4 D488D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr1:75072309 G>A maps to NM_001002912.4 D488D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr1:90398914 C>T maps to NM_001134479.1 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr1:90398914 C>T maps to NM_001134479.1 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr1:151260524 G>A maps to NM_020832.1 K586K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr1:151260524 G>A maps to NM_020832.1 K586K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr1:247597515 C>T maps to NM_004895.4 F813F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr1:247597515 C>T maps to NM_004895.4 F813F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr10:11308600 G>A maps to NM_006561.3 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr10:11308600 G>A maps to NM_006561.3 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr11:6648365 A>G maps to NM_003737.2 R1968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr11:6648365 A>G maps to NM_003737.2 R1968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr11:68566775 C>T maps to NM_001876.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr11:68566775 C>T maps to NM_001876.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr12:21692266 G>A maps to NM_021957.3 Y605Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr12:21692266 G>A maps to NM_021957.3 Y605Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr12:76767186 A>G maps to NM_020841.4 V618V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr12:76767186 A>G maps to NM_020841.4 V618V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr13:84453706 G>A maps to NM_052910.1 R646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr13:84453706 G>A maps to NM_052910.1 R646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr15:74630345 G>A maps to NM_000781.2 F511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr15:74630345 G>A maps to NM_000781.2 F511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr16:129428 C>T maps to NM_002434.2 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr16:129428 C>T maps to NM_002434.2 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr16:10273896 G>A maps to NM_000833.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr16:10273896 G>A maps to NM_000833.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr17:3572586 C>G maps to NM_031298.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr17:3572586 C>G maps to NM_031298.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr17:7576852 C>T maps to NM_001126112.1 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr17:7576852 C>T maps to NM_001126112.1 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr17:34079821 C>A maps to NM_139285.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr17:34079821 C>A maps to NM_139285.2 P16P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CV-5977-01A-11D-1683-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CV-5977-01A-11D-1683-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr19:4679885 G>A maps to ENST00000357909 V928V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr19:4679885 G>A maps to ENST00000357909 V928V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr19:8807821 G>A maps to NM_178525.3 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr19:8807821 G>A maps to NM_178525.3 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr19:11598500 G>T maps to NM_138783.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr19:11598500 G>T maps to NM_138783.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr2:38301496 G>A maps to NM_000104.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr2:38301496 G>A maps to NM_000104.3 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr2:73447179 C>T maps to NM_006062.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr2:73447179 C>T maps to NM_006062.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr2:74902407 C>T maps to NM_004263.3 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr2:74902407 C>T maps to NM_004263.3 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr2:152539187 G>A maps to NM_001164507.1 D977D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr2:152539187 G>A maps to NM_001164507.1 D977D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr2:179642180 G>T maps to NM_133378.4 G1537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr2:179642180 G>T maps to NM_133378.4 G1537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr2:179647598 G>A maps to NM_133378.4 R1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr2:179647598 G>A maps to NM_133378.4 R1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr3:52819103 T>C maps to NM_002215.2 D484D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr3:52819103 T>C maps to NM_002215.2 D484D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr3:180322056 G>A maps to NM_133462.3 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr3:180322056 G>A maps to NM_133462.3 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr3:194947477 G>A maps to NM_152531.4 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr3:194947477 G>A maps to NM_152531.4 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr5:81549159 G>C maps to NM_031482.4 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr5:81549159 G>C maps to NM_031482.4 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr5:161569194 C>G maps to NM_198903.2 Y305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr5:161569194 C>G maps to NM_198903.2 Y305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr5:167896015 C>T maps to NM_001161661.1 D1118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr5:167896015 C>T maps to NM_001161661.1 D1118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr5:178416068 C>T maps to NM_000843.3 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr5:178416068 C>T maps to NM_000843.3 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr6:46846092 C>T maps to NM_015234.4 K362K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr6:46846092 C>T maps to NM_015234.4 K362K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr7:5540951 C>T maps to ENST00000312577 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr7:5540951 C>T maps to ENST00000312577 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr7:94056510 T>C maps to NM_000089.3 G1057G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr7:94056510 T>C maps to NM_000089.3 G1057G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr8:3611464 G>A maps to NM_033225.5 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr8:3611464 G>A maps to NM_033225.5 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr8:17611495 G>T maps to NM_001001924.2 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr8:17611495 G>T maps to NM_001001924.2 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr8:133978853 C>A maps to NM_003235.4 V1866V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr8:133978853 C>A maps to NM_003235.4 V1866V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr9:116267801 C>T maps to NM_144488.4 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr9:116267801 C>T maps to NM_144488.4 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr9:136307840 C>T maps to NM_139025.3 C737C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chr9:136307840 C>T maps to NM_139025.3 C737C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chrX:128887211 C>G maps to NM_003399.5 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5977-01A-11D-1683-08 chrX:128887211 C>G maps to NM_003399.5 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr1:1273763 C>A maps to ENST00000378888 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr1:1273763 C>A maps to ENST00000378888 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr1:160124905 C>A maps to NM_144699.3 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr1:160124905 C>A maps to NM_144699.3 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr1:207646234 A>G maps to NM_001006658.2 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr1:207646234 A>G maps to NM_001006658.2 G563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr10:27703079 G>A maps to NM_001034842.3 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr10:27703079 G>A maps to NM_001034842.3 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr10:51748543 G>T maps to NM_001077665.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr10:51748543 G>T maps to NM_001077665.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr11:7960206 C>T maps to NM_001003745.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr11:7960206 C>T maps to NM_001003745.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr11:56510759 G>A maps to NM_001005284.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr11:56510759 G>A maps to NM_001005284.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr11:89135492 C>A did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr11:89135492 C>A did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr11:119059094 G>T maps to ENST00000392817 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr11:119059094 G>T maps to ENST00000392817 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr11:123753940 T>C maps to NM_001013743.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr11:123753940 T>C maps to NM_001013743.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:7649407 C>G did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:7649407 C>G did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:11034866 T>A maps to NM_006250.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:11034866 T>A maps to NM_006250.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:19475472 C>T maps to ENST00000429027 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:19475472 C>T maps to ENST00000429027 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:33532865 G>T maps to NM_198992.3 C467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:33532865 G>T maps to NM_198992.3 C467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:40734241 C>G maps to NM_198578.3 S2032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:40734241 C>G maps to NM_198578.3 S2032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:85680629 G>C did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:85680629 G>C did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:105515901 G>A maps to NM_015275.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:105515901 G>A maps to NM_015275.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:108959131 T>C maps to NM_213595.2 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr12:108959131 T>C maps to NM_213595.2 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr13:103520607 G>C did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr13:103520607 G>C did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr14:31071099 G>T maps to NM_017769.3 G293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr14:31071099 G>T maps to NM_017769.3 G293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr14:59105249 G>T maps to NM_016651.5 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr14:59105249 G>T maps to NM_016651.5 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr14:69808450 G>A maps to NM_020692.2 W414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr14:69808450 G>A maps to NM_020692.2 W414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr14:70633618 G>T maps to NM_183002.1 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr14:70633618 G>T maps to NM_183002.1 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr14:96797951 T>C maps to NM_018036.5 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr14:96797951 T>C maps to NM_018036.5 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr15:32926131 A>G did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr15:32926131 A>G did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr16:66642246 G>A maps to NM_181553.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr16:66642246 G>A maps to NM_181553.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr17:9674888 G>A maps to ENST00000330255 Y285Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr17:9674888 G>A maps to ENST00000330255 Y285Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr18:14106205 T>C maps to NM_145287.3 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr18:14106205 T>C maps to NM_145287.3 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr18:40323625 G>T maps to NM_002930.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr18:40323625 G>T maps to NM_002930.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr19:608034 C>T maps to NM_001194.3 Y430Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr19:608034 C>T maps to NM_001194.3 Y430Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr19:6709692 A>T did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr19:6709692 A>T did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr19:16977363 C>T maps to NM_015260.1 D633D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr19:16977363 C>T maps to NM_015260.1 D633D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr19:33131244 T>C maps to NM_032139.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr19:33131244 T>C maps to NM_032139.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr19:36430642 C>T maps to NM_024509.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr19:36430642 C>T maps to NM_024509.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr2:127447861 C>A maps to NM_002101.3 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr2:127447861 C>A maps to NM_002101.3 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr2:128262821 A>G maps to NM_017969.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr2:128262821 A>G maps to NM_017969.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr2:220501090 C>G maps to NM_201574.2 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr2:220501090 C>G maps to NM_201574.2 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr20:18379175 C>T maps to NM_001099407.1 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr20:18379175 C>T maps to NM_001099407.1 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr22:38016246 T>C maps to ENST00000381756 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr22:38016246 T>C maps to ENST00000381756 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr3:9027553 C>A maps to NM_014850.2 T983T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr3:9027553 C>A maps to NM_014850.2 T983T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr3:147113699 C>A maps to NM_001168379.1 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr3:147113699 C>A maps to NM_001168379.1 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr3:170198782 G>A maps to NM_020949.2 R430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr3:170198782 G>A maps to NM_020949.2 R430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr4:122836026 G>A maps to NM_001130698.1 Q417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr4:122836026 G>A maps to NM_001130698.1 Q417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr4:123249347 G>C maps to NM_015312.3 V3695V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr4:123249347 G>C maps to NM_015312.3 V3695V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr4:177071266 A>G maps to NM_170710.4 E731E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr4:177071266 A>G maps to NM_170710.4 E731E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr5:13788882 C>T maps to NM_001369.2 V2863V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr5:13788882 C>T maps to NM_001369.2 V2863V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr5:13885170 A>C maps to NM_001369.2 L970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr5:13885170 A>C maps to NM_001369.2 L970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr6:34741319 G>A maps to ENST00000374017 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr6:34741319 G>A maps to ENST00000374017 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr6:49425486 C>A maps to NM_000255.3 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr6:49425486 C>A maps to NM_000255.3 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr7:106898717 C>T maps to NM_006348.3 K593K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr7:106898717 C>T maps to NM_006348.3 K593K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr8:2855569 G>A maps to NM_033225.5 S2780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr8:2855569 G>A maps to NM_033225.5 S2780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr8:8998839 C>A maps to NM_024607.2 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr8:8998839 C>A maps to NM_024607.2 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr8:53570559 T>A maps to NM_014781.4 K640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr8:53570559 T>A maps to NM_014781.4 K640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr8:103564143 C>G maps to NM_024410.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr8:103564143 C>G maps to NM_024410.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr8:113585862 C>T maps to NM_198123.1 T1303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr8:113585862 C>T maps to NM_198123.1 T1303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr8:113599378 G>T maps to NM_198123.1 C1267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr8:113599378 G>T maps to NM_198123.1 C1267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr9:101907134 T>C maps to NM_004612.2 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr9:101907134 T>C maps to NM_004612.2 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr9:116185749 G>T maps to ENST00000451722 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr9:116185749 G>T maps to ENST00000451722 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr9:133799268 T>A did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chr9:133799268 T>A did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chrX:18972376 C>A maps to NM_000292.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chrX:18972376 C>A maps to NM_000292.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chrX:34150047 C>A maps to NM_203408.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chrX:34150047 C>A maps to NM_203408.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chrX:39913586 C>T did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chrX:39913586 C>T did not map to a codon.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chrX:53619396 G>A maps to ENST00000276009 S1311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chrX:53619396 G>A maps to ENST00000276009 S1311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chrX:54985327 G>T maps to NM_002625.2 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chrX:54985327 G>T maps to NM_002625.2 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chrX:73962021 C>A maps to NM_001008537.2 T790T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chrX:73962021 C>A maps to NM_001008537.2 T790T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr1:172411035 G>A maps to NM_153747.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr1:172411035 G>A maps to NM_153747.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr11:198283 A>G maps to NM_053280.3 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr11:198283 A>G maps to NM_053280.3 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr17:39740134 G>T maps to NM_000526.4 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr17:39740134 G>T maps to NM_000526.4 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr17:48447948 T>A did not map to a codon.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr17:48447948 T>A did not map to a codon.
Multiple mappings detected for codon TCGA-CV-5979-01A-11D-1683-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CV-5979-01A-11D-1683-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr19:1818780 G>A maps to NM_020695.3 N942N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr19:1818780 G>A maps to NM_020695.3 N942N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr20:62328364 G>A maps to ENST00000482936 L1384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr20:62328364 G>A maps to ENST00000482936 L1384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr3:51198104 G>T maps to NM_004947.4 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr3:51198104 G>T maps to NM_004947.4 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr6:10529617 G>A maps to NM_145649.4 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr6:10529617 G>A maps to NM_145649.4 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr6:31557387 A>C maps to NM_147130.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr6:31557387 A>C maps to NM_147130.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr6:139167807 G>A maps to NM_001195037.2 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5979-01A-11D-1683-08 chr6:139167807 G>A maps to NM_001195037.2 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr1:22169403 C>T maps to NM_005529.5 L2923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr1:22169403 C>T maps to NM_005529.5 L2923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr1:42628621 C>T maps to NM_033553.2 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr1:42628621 C>T maps to NM_033553.2 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr1:120539833 A>T maps to NM_024408.2 C179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr1:120539833 A>T maps to NM_024408.2 C179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr1:182555478 G>A maps to NM_021133.3 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr1:182555478 G>A maps to NM_021133.3 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr1:240256065 A>G maps to ENST00000406993 Q362Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr1:240256065 A>G maps to ENST00000406993 Q362Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr11:6704512 G>C maps to NM_022061.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr11:6704512 G>C maps to NM_022061.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr11:20119262 G>A maps to ENST00000396087 E2110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr11:20119262 G>A maps to ENST00000396087 E2110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr11:56432081 A>G maps to NM_001004730.1 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr11:56432081 A>G maps to NM_001004730.1 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr11:75152210 G>A maps to NM_030792.6 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr11:75152210 G>A maps to NM_030792.6 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr12:52627277 C>T maps to NM_005556.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr12:52627277 C>T maps to NM_005556.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr13:113728843 G>A maps to NM_001112732.1 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr13:113728843 G>A maps to NM_001112732.1 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr14:95570036 G>A maps to NM_177438.2 S1232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr14:95570036 G>A maps to NM_177438.2 S1232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr16:31091298 C>T maps to NM_014699.3 L1218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr16:31091298 C>T maps to NM_014699.3 L1218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr16:51174002 G>A maps to ENST00000251020 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr16:51174002 G>A maps to ENST00000251020 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr16:57719692 G>A maps to NM_170776.4 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr16:57719692 G>A maps to NM_170776.4 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr17:34001259 G>A maps to NM_001030006.1 G748G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr17:34001259 G>A maps to NM_001030006.1 G748G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr18:63547694 C>T maps to NM_004361.2 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr18:63547694 C>T maps to NM_004361.2 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr19:17004116 G>A maps to ENST00000443236 S1877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr19:17004116 G>A maps to ENST00000443236 S1877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr19:53644778 G>A maps to NM_001172674.1 C435C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr19:53644778 G>A maps to NM_001172674.1 C435C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr2:129026287 C>T maps to NM_004807.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr2:129026287 C>T maps to NM_004807.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr20:25262743 G>T maps to NM_002862.3 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr20:25262743 G>T maps to NM_002862.3 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr3:185347617 C>T maps to ENST00000427465 Q661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr3:185347617 C>T maps to ENST00000427465 Q661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr5:26885756 G>A maps to NM_016279.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr5:26885756 G>A maps to NM_016279.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr7:5097369 G>A maps to NM_021163.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr7:5097369 G>A maps to NM_021163.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr7:123516944 G>A maps to NM_012269.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr7:123516944 G>A maps to NM_012269.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr9:21970999 C>A maps to NM_001195132.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr9:21970999 C>A maps to NM_001195132.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr9:113170490 G>C maps to ENST00000374463 L2466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr9:113170490 G>C maps to ENST00000374463 L2466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chrX:73524499 C>A maps to NM_203303.2 C133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chrX:73524499 C>A maps to NM_203303.2 C133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chrX:101396189 C>T maps to NM_001006938.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chrX:101396189 C>T maps to NM_001006938.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chrX:144337189 G>A did not map to a codon.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chrX:144337189 G>A did not map to a codon.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr1:156563321 C>T maps to ENST00000446584 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr1:156563321 C>T maps to ENST00000446584 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr1:236924421 C>T maps to NM_001103.2 T825T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr1:236924421 C>T maps to NM_001103.2 T825T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr10:117823943 G>A maps to NM_005264.4 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr10:117823943 G>A maps to NM_005264.4 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr15:51981444 A>G maps to NM_013243.3 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr15:51981444 A>G maps to NM_013243.3 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr16:64984709 G>A maps to NM_001797.2 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr16:64984709 G>A maps to NM_001797.2 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr16:66974468 G>A maps to NM_003869.5 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr16:66974468 G>A maps to NM_003869.5 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr19:9088748 G>C maps to NM_024690.2 L1022L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr19:9088748 G>C maps to NM_024690.2 L1022L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr19:16284286 G>A did not map to a codon.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr19:16284286 G>A did not map to a codon.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr19:18555653 T>A maps to NM_006532.3 K592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr19:18555653 T>A maps to NM_006532.3 K592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr3:169540269 C>G maps to NM_001080460.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr3:169540269 C>G maps to NM_001080460.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr4:68610289 G>A maps to NM_000406.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr4:68610289 G>A maps to NM_000406.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr4:154249704 C>T maps to NM_015271.3 F682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr4:154249704 C>T maps to NM_015271.3 F682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr6:7571656 C>T maps to NM_004415.2 A581A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr6:7571656 C>T maps to NM_004415.2 A581A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr6:116288717 T>C maps to NM_002031.2 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr6:116288717 T>C maps to NM_002031.2 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr6:145093096 A>G maps to NM_007124.2 Q2850Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr6:145093096 A>G maps to NM_007124.2 Q2850Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr7:143826963 C>T maps to NM_001001659.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr7:143826963 C>T maps to NM_001001659.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr8:27327421 C>T maps to NM_000742.3 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr8:27327421 C>T maps to NM_000742.3 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr8:67929967 G>T maps to ENST00000421742 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr8:67929967 G>T maps to ENST00000421742 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr8:144295189 G>T maps to NM_178172.3 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr8:144295189 G>T maps to NM_178172.3 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr9:40774006 G>T maps to NM_033160.5 S423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr9:40774006 G>T maps to NM_033160.5 S423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr9:139974546 C>T maps to NM_207309.2 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr9:139974546 C>T maps to NM_207309.2 N377N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr1:152187758 G>A maps to NM_001009931.1 Q2116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr1:152187758 G>A maps to NM_001009931.1 Q2116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr10:28413007 G>A maps to NM_173496.3 N189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr10:28413007 G>A maps to NM_173496.3 N189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr10:122622271 C>T maps to NM_018117.11 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr10:122622271 C>T maps to NM_018117.11 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr11:11986064 C>T maps to ENST00000450094 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr11:11986064 C>T maps to ENST00000450094 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr11:47833635 A>G maps to NM_015231.1 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr11:47833635 A>G maps to NM_015231.1 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr12:99007410 C>T maps to NM_201612.1 E335E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr12:99007410 C>T maps to NM_201612.1 E335E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr15:25961900 C>T maps to NM_024490.3 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr15:25961900 C>T maps to NM_024490.3 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr16:10032165 C>T maps to NM_000833.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr16:10032165 C>T maps to NM_000833.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr16:49430550 C>T maps to NM_144602.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr16:49430550 C>T maps to NM_144602.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr17:7673915 C>T maps to NM_020877.2 L1380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr17:7673915 C>T maps to NM_020877.2 L1380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr19:2271953 G>A did not map to a codon.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr19:2271953 G>A did not map to a codon.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr19:5772835 G>T maps to NM_152784.3 E601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr19:5772835 G>T maps to NM_152784.3 E601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr19:15769112 T>C maps to NM_000896.2 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr19:15769112 T>C maps to NM_000896.2 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr19:52519598 G>A maps to NM_025040.3 Q418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr19:52519598 G>A maps to NM_025040.3 Q418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr20:61511733 G>A maps to NM_033081.2 A1858A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr20:61511733 G>A maps to NM_033081.2 A1858A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr22:19960525 G>A maps to NM_001670.2 H824H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr22:19960525 G>A maps to NM_001670.2 H824H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr22:38121553 C>T maps to NM_001039141.2 P997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr22:38121553 C>T maps to NM_001039141.2 P997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr22:41753276 G>C maps to ENST00000351589 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr22:41753276 G>C maps to ENST00000351589 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr3:8609124 G>A did not map to a codon.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr3:8609124 G>A did not map to a codon.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr4:88035994 G>A maps to NM_001166693.1 V670V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr4:88035994 G>A maps to NM_001166693.1 V670V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr5:137593488 G>A maps to NM_001496.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr5:137593488 G>A maps to NM_001496.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr5:137762665 C>T maps to NM_016604.3 R1472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr5:137762665 C>T maps to NM_016604.3 R1472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr6:75950912 C>T maps to NM_001865.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr6:75950912 C>T maps to NM_001865.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr6:145021234 G>A maps to NM_007124.2 E2555E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr6:145021234 G>A maps to NM_007124.2 E2555E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr7:89915650 G>T maps to NM_001039706.2 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr7:89915650 G>T maps to NM_001039706.2 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr7:104801042 C>A maps to ENST00000336613 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr7:104801042 C>A maps to ENST00000336613 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr7:149461820 C>T maps to NM_207336.1 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr7:149461820 C>T maps to NM_207336.1 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr9:21970999 C>A maps to NM_001195132.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr9:21970999 C>A maps to NM_001195132.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr9:86905134 G>A maps to NM_022127.2 H361H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr9:86905134 G>A maps to NM_022127.2 H361H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr9:116930230 C>T maps to NM_032888.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6436-01A-11D-1683-08 chr9:116930230 C>T maps to NM_032888.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:25611199 C>T maps to ENST00000357542 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:25611199 C>T maps to ENST00000357542 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:85630215 G>A maps to NM_032184.1 L1026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:85630215 G>A maps to NM_032184.1 L1026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:103480095 G>A maps to NM_080629.2 Q527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:103480095 G>A maps to NM_080629.2 Q527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:107691397 G>A maps to NM_001113226.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:107691397 G>A maps to NM_001113226.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:110086036 C>G maps to NM_031936.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:110086036 C>G maps to NM_031936.4 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:154573539 C>T maps to ENST00000292205 Q569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:154573539 C>T maps to ENST00000292205 Q569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:200377872 G>A maps to NM_012482.3 Q321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:200377872 G>A maps to NM_012482.3 Q321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:202287785 C>G maps to NM_001017403.1 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:202287785 C>G maps to NM_001017403.1 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:212115324 C>T maps to NM_015434.3 V910V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr1:212115324 C>T maps to NM_015434.3 V910V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:17147563 A>T maps to NM_001081.3 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:17147563 A>T maps to NM_001081.3 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:17278347 G>A maps to NM_003380.3 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:17278347 G>A maps to NM_003380.3 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:25284721 C>T maps to NM_145010.2 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:25284721 C>T maps to NM_145010.2 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:95892094 C>G maps to ENST00000371380 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:95892094 C>G maps to ENST00000371380 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:120094624 C>A did not map to a codon.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:120094624 C>A did not map to a codon.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:135020756 C>T maps to ENST00000368572 L1234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:135020756 C>T maps to ENST00000368572 L1234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr11:57100269 G>A maps to NM_003146.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr11:57100269 G>A maps to NM_003146.2 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr11:60689393 G>C maps to NM_024092.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr11:60689393 G>C maps to NM_024092.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr11:123601371 C>T maps to NM_003455.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr11:123601371 C>T maps to NM_003455.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr12:49433387 G>A maps to NM_003482.3 R2687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr12:49433387 G>A maps to NM_003482.3 R2687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr12:52884659 C>T maps to NM_005554.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr12:52884659 C>T maps to NM_005554.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr12:112097071 C>T maps to NM_006768.3 E350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr12:112097071 C>T maps to NM_006768.3 E350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr13:36050181 G>T maps to NM_005584.4 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr13:36050181 G>T maps to NM_005584.4 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr14:105412106 G>C maps to NM_138420.2 P3227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr14:105412106 G>C maps to NM_138420.2 P3227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr15:54914564 T>C maps to ENST00000260323 H2049H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr15:54914564 T>C maps to ENST00000260323 H2049H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr15:65490838 T>C maps to NM_003613.3 E595E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr15:65490838 T>C maps to NM_003613.3 E595E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr15:74922108 T>G maps to NM_001130028.1 L601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr15:74922108 T>G maps to NM_001130028.1 L601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr15:101445831 C>G maps to NM_000693.2 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr15:101445831 C>G maps to NM_000693.2 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr16:2273706 G>A maps to NM_004424.3 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr16:2273706 G>A maps to NM_004424.3 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr16:28844639 C>T maps to NM_148414.1 I640I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr16:28844639 C>T maps to NM_148414.1 I640I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr17:7736072 C>T maps to NM_020877.2 N4301N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr17:7736072 C>T maps to NM_020877.2 N4301N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr17:18062989 G>A maps to ENST00000205890 L3100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr17:18062989 G>A maps to ENST00000205890 L3100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr17:67287393 C>T maps to ENST00000392677 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr17:67287393 C>T maps to ENST00000392677 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr17:72348996 C>G maps to NM_153209.3 S673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr17:72348996 C>G maps to NM_153209.3 S673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr17:79667587 C>T maps to NM_004712.4 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr17:79667587 C>T maps to NM_004712.4 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr17:79847181 C>T maps to NM_005782.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr17:79847181 C>T maps to NM_005782.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr18:29450922 T>C maps to NM_014939.3 S741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr18:29450922 T>C maps to NM_014939.3 S741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr18:74154473 G>A maps to ENST00000443185 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr18:74154473 G>A maps to ENST00000443185 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:3192651 C>T maps to NM_020170.3 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:3192651 C>T maps to NM_020170.3 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:3964691 G>C maps to NM_001348.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:3964691 G>C maps to NM_001348.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:11233895 A>G maps to NM_000527.4 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:11233895 A>G maps to NM_000527.4 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:15132718 G>A maps to NM_173482.2 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:15132718 G>A maps to NM_173482.2 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:19431287 G>A maps to NM_172231.2 D6D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:19431287 G>A maps to NM_172231.2 D6D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:42557774 G>A maps to NM_002088.3 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:42557774 G>A maps to NM_002088.3 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:43269719 G>C maps to NM_182707.2 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:43269719 G>C maps to NM_182707.2 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:56413453 G>C maps to NM_176810.2 V912V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr19:56413453 G>C maps to NM_176810.2 V912V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr2:43808910 C>T maps to ENST00000330266 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr2:43808910 C>T maps to ENST00000330266 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr2:108626800 T>C maps to NM_021815.2 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr2:108626800 T>C maps to NM_021815.2 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr2:141598640 G>A maps to NM_018557.2 L1654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr2:141598640 G>A maps to NM_018557.2 L1654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr2:160206344 T>C maps to NM_013450.2 S1579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr2:160206344 T>C maps to NM_013450.2 S1579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr2:191872312 C>A maps to NM_007315.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr2:191872312 C>A maps to NM_007315.3 L116L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CV-6441-01A-11D-1683-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-CV-6441-01A-11D-1683-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr2:234602465 C>T maps to NM_001072.3 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr2:234602465 C>T maps to NM_001072.3 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr20:24993468 G>A maps to NM_032501.2 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr20:24993468 G>A maps to NM_032501.2 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr20:35532576 C>A maps to NM_015474.3 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr20:35532576 C>A maps to NM_015474.3 E496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr22:18387473 G>A maps to NM_015241.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr22:18387473 G>A maps to NM_015241.2 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr22:18387599 G>A maps to NM_015241.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr22:18387599 G>A maps to NM_015241.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr22:41240913 C>T did not map to a codon.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr22:41240913 C>T did not map to a codon.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr22:43898629 C>A maps to NM_001044370.1 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr22:43898629 C>A maps to NM_001044370.1 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr22:50724680 G>A maps to NM_012401.2 R600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr22:50724680 G>A maps to NM_012401.2 R600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr3:112358038 C>T maps to ENST00000447230 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr3:112358038 C>T maps to ENST00000447230 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr3:113955699 C>T maps to NM_007136.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr3:113955699 C>T maps to NM_007136.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr4:68703946 G>A maps to NM_004262.2 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr4:68703946 G>A maps to NM_004262.2 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr4:125592803 G>C maps to NM_020337.2 S543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr4:125592803 G>C maps to NM_020337.2 S543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr4:187627829 G>C maps to ENST00000260147 S1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr4:187627829 G>C maps to ENST00000260147 S1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr5:1489928 G>A maps to NM_024830.3 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr5:1489928 G>A maps to NM_024830.3 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr5:37371158 G>C did not map to a codon.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr5:37371158 G>C did not map to a codon.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr5:43453837 T>A maps to NM_022483.4 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr5:43453837 T>A maps to NM_022483.4 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr5:79095240 G>A maps to NM_153610.3 E4004E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr5:79095240 G>A maps to NM_153610.3 E4004E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr5:121411145 G>A maps to NM_002317.5 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr5:121411145 G>A maps to NM_002317.5 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr5:159821612 C>G maps to NM_022090.3 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr5:159821612 C>G maps to NM_022090.3 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr6:2623873 G>A maps to NM_152554.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr6:2623873 G>A maps to NM_152554.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr6:27114364 G>A maps to NM_080593.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr6:27114364 G>A maps to NM_080593.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr6:105606560 G>A maps to NM_022361.4 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr6:105606560 G>A maps to NM_022361.4 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr6:158540195 G>A maps to NM_032861.3 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr6:158540195 G>A maps to NM_032861.3 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr7:42079707 C>T maps to NM_000168.5 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr7:42079707 C>T maps to NM_000168.5 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr7:81355325 G>A maps to NM_000601.4 R350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr7:81355325 G>A maps to NM_000601.4 R350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr7:100806474 G>A maps to NM_003378.3 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr7:100806474 G>A maps to NM_003378.3 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr7:150878412 T>C maps to ENST00000422024 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr7:150878412 T>C maps to ENST00000422024 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr8:48887406 T>A maps to NM_182746.1 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr8:48887406 T>A maps to NM_182746.1 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr8:81899629 C>T maps to NM_018440.3 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr8:81899629 C>T maps to NM_018440.3 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr8:110590242 A>G maps to NM_001099744.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr8:110590242 A>G maps to NM_001099744.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr9:18753313 G>A maps to NM_001040272.4 W675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr9:18753313 G>A maps to NM_001040272.4 W675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chrX:1471250 G>A maps to NM_002183.2 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chrX:1471250 G>A maps to NM_002183.2 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr1:99772514 T>C maps to NM_014839.4 T747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr1:99772514 T>C maps to NM_014839.4 T747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr1:248551196 C>A maps to NM_001005471.1 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr1:248551196 C>A maps to NM_001005471.1 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr11:5142745 G>A maps to NM_001005222.2 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr11:5142745 G>A maps to NM_001005222.2 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr11:55761645 C>A maps to NM_003697.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr11:55761645 C>A maps to NM_003697.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr11:123811174 T>C maps to NM_001001965.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr11:123811174 T>C maps to NM_001001965.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr12:9353587 G>C maps to NM_002864.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr12:9353587 G>C maps to NM_002864.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr12:32886734 T>C maps to ENST00000381000 N524N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr12:32886734 T>C maps to ENST00000381000 N524N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr12:55714811 T>G maps to NM_001005182.1 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr12:55714811 T>G maps to NM_001005182.1 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr12:104732984 G>A maps to NM_001093771.1 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr12:104732984 G>A maps to NM_001093771.1 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr13:111102706 C>G maps to NM_001846.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr13:111102706 C>G maps to NM_001846.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr14:76549918 G>C maps to NM_052873.2 *214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr14:76549918 G>C maps to NM_052873.2 *214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr15:55838316 T>A maps to NM_015617.1 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr15:55838316 T>A maps to NM_015617.1 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr18:48252450 C>T maps to NM_002747.3 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr18:48252450 C>T maps to NM_002747.3 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr18:64172066 T>A maps to NM_021153.2 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr18:64172066 T>A maps to NM_021153.2 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr19:8191466 C>T maps to NM_032447.3 W813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr19:8191466 C>T maps to NM_032447.3 W813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr19:50881484 C>T maps to NM_007121.4 C87C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr19:50881484 C>T maps to NM_007121.4 C87C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr2:15415922 C>T maps to NM_015909.2 L1803L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr2:15415922 C>T maps to NM_015909.2 L1803L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr2:141299369 A>T maps to NM_018557.2 A2455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr2:141299369 A>T maps to NM_018557.2 A2455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr20:33524590 G>A maps to NM_000178.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr20:33524590 G>A maps to NM_000178.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr22:20127040 G>A maps to NM_013373.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr22:20127040 G>A maps to NM_013373.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr4:88584471 G>C maps to NM_004407.3 *514Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr4:88584471 G>C maps to NM_004407.3 *514Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr4:96761918 C>T maps to NM_005390.4 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr4:96761918 C>T maps to NM_005390.4 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr5:79027401 T>C maps to NM_153610.3 D938D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr5:79027401 T>C maps to NM_153610.3 D938D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr5:156741392 G>A maps to ENST00000442283 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr5:156741392 G>A maps to ENST00000442283 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr5:176519732 A>G maps to NM_213647.1 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr5:176519732 A>G maps to NM_213647.1 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr6:26205024 C>A maps to NM_003545.3 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr6:26205024 C>A maps to NM_003545.3 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr6:90097154 G>T maps to NM_021244.4 C101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr6:90097154 G>T maps to NM_021244.4 C101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr6:117724425 C>T maps to NM_002944.2 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr6:117724425 C>T maps to NM_002944.2 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr7:11675952 T>A maps to ENST00000423059 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr7:11675952 T>A maps to ENST00000423059 R276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr7:23825128 A>G maps to NM_031414.3 E727E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr7:23825128 A>G maps to NM_031414.3 E727E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr7:44556433 G>A maps to NM_013389.2 L1156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr7:44556433 G>A maps to NM_013389.2 L1156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr7:72413633 G>A maps to ENST00000434423 T1034T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr7:72413633 G>A maps to ENST00000434423 T1034T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr7:87913171 G>C maps to NM_024636.2 S138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr7:87913171 G>C maps to NM_024636.2 S138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr8:25154151 C>T maps to NM_024940.6 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr8:25154151 C>T maps to NM_024940.6 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr8:105361224 C>T maps to NM_030788.2 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr8:105361224 C>T maps to NM_030788.2 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr8:139601579 G>A maps to NM_152888.1 P1599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr8:139601579 G>A maps to NM_152888.1 P1599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr8:146107268 C>G maps to NM_021061.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr8:146107268 C>G maps to NM_021061.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr9:118997916 G>T did not map to a codon.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chr9:118997916 G>T did not map to a codon.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chrX:5811510 A>G maps to ENST00000381093 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chrX:5811510 A>G maps to ENST00000381093 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chrX:34961337 C>T maps to NM_152631.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chrX:34961337 C>T maps to NM_152631.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chrX:107924155 G>T maps to ENST00000328300 E1353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6933-01A-11D-1912-08 chrX:107924155 G>T maps to ENST00000328300 E1353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr1:33502360 A>G maps to NM_001625.3 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr1:33502360 A>G maps to NM_001625.3 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr1:111778260 G>T maps to NM_004000.2 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr1:111778260 G>T maps to NM_004000.2 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr1:183095287 G>A maps to NM_002293.3 G945G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr1:183095287 G>A maps to NM_002293.3 G945G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr1:196197395 G>T maps to NM_198503.2 C1122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr1:196197395 G>T maps to NM_198503.2 C1122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr10:106960975 A>C maps to NM_014978.1 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr10:106960975 A>C maps to NM_014978.1 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr11:9759762 C>T maps to NM_015055.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr11:9759762 C>T maps to NM_015055.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr11:66626405 C>T maps to NM_024036.4 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr11:66626405 C>T maps to NM_024036.4 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr11:85712202 T>A did not map to a codon.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr11:85712202 T>A did not map to a codon.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr11:102709883 G>A maps to NM_002422.3 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr11:102709883 G>A maps to NM_002422.3 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr11:103022984 G>T maps to NM_001080463.1 E1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr11:103022984 G>T maps to NM_001080463.1 E1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr12:124268651 C>T maps to NM_207437.3 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr12:124268651 C>T maps to NM_207437.3 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr15:66828268 A>T did not map to a codon.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr15:66828268 A>T did not map to a codon.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr16:29884952 C>A maps to NM_201575.2 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr16:29884952 C>A maps to NM_201575.2 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr17:54428210 C>T maps to NM_153228.2 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr17:54428210 C>T maps to NM_153228.2 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr17:73500709 C>T maps to NM_020753.3 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr17:73500709 C>T maps to NM_020753.3 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr18:13885390 G>A maps to NM_000529.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr18:13885390 G>A maps to NM_000529.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr19:11038314 G>A maps to NM_024029.3 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr19:11038314 G>A maps to NM_024029.3 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr19:44590485 G>A maps to NM_001037813.2 K285K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr19:44590485 G>A maps to NM_001037813.2 K285K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr19:54965697 C>T maps to ENST00000431846 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr19:54965697 C>T maps to ENST00000431846 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr19:55995169 G>A maps to NM_033113.2 V866V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr19:55995169 G>A maps to NM_033113.2 V866V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr22:45574200 C>T maps to NM_007172.3 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr22:45574200 C>T maps to NM_007172.3 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr5:11082865 G>A maps to NM_001332.2 C910C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr5:11082865 G>A maps to NM_001332.2 C910C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr6:26250637 G>A maps to NM_021018.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr6:26250637 G>A maps to NM_021018.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr6:32020729 C>T maps to ENST00000375244 T2944T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr6:32020729 C>T maps to ENST00000375244 T2944T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr6:32906578 C>T maps to NM_002118.4 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr6:32906578 C>T maps to NM_002118.4 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr7:5103362 A>G maps to NM_021163.3 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr7:5103362 A>G maps to NM_021163.3 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr7:97821897 C>T maps to NM_014916.3 H707H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr7:97821897 C>T maps to NM_014916.3 H707H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr8:77763206 G>C maps to NM_024721.4 P1350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chr8:77763206 G>C maps to NM_024721.4 P1350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chrX:151283637 T>G maps to NM_021049.3 *125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6934-01A-11D-1912-08 chrX:151283637 T>G maps to NM_021049.3 *125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:16380199 A>G maps to NM_000085.3 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:16380199 A>G maps to NM_000085.3 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:47717389 G>A maps to NM_001048166.1 S1095S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:47717389 G>A maps to NM_001048166.1 S1095S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:66081723 C>T maps to NM_002303.5 Q677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:66081723 C>T maps to NM_002303.5 Q677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:114216017 G>A maps to NM_001142782.1 E1040E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:114216017 G>A maps to NM_001142782.1 E1040E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:151315025 G>C maps to NM_000449.3 S496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:151315025 G>C maps to NM_000449.3 S496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:161022563 G>A maps to NM_001025598.1 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:161022563 G>A maps to NM_001025598.1 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:161719653 C>T maps to NM_007240.1 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:161719653 C>T maps to NM_007240.1 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:170688865 G>C did not map to a codon.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:170688865 G>C did not map to a codon.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:171509617 G>T maps to ENST00000392078 E1005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:171509617 G>T maps to ENST00000392078 E1005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:185946935 C>T maps to NM_031935.2 Q797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:185946935 C>T maps to NM_031935.2 Q797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:248569513 C>A maps to NM_030904.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr1:248569513 C>A maps to NM_030904.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr10:47087601 C>A maps to NM_005972.4 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr10:47087601 C>A maps to NM_005972.4 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr10:88836357 C>T maps to NM_005271.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr10:88836357 C>T maps to NM_005271.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr10:105893539 A>G maps to ENST00000389588 T1479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr10:105893539 A>G maps to ENST00000389588 T1479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr11:7818033 A>G maps to NM_153444.1 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr11:7818033 A>G maps to NM_153444.1 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr11:68154174 G>A maps to NM_002335.2 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr11:68154174 G>A maps to NM_002335.2 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr11:76916512 C>T maps to NM_000260.3 S1829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr11:76916512 C>T maps to NM_000260.3 S1829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr12:31435798 C>T maps to NM_001135812.1 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr12:31435798 C>T maps to NM_001135812.1 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr12:91502198 G>C maps to NM_002345.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr12:91502198 G>C maps to NM_002345.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr12:112622227 G>A maps to NM_001109662.2 A3342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr12:112622227 G>A maps to NM_001109662.2 A3342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr12:121438952 C>A maps to NM_000545.5 I618I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr12:121438952 C>A maps to NM_000545.5 I618I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr13:39446955 G>T maps to NM_207361.4 G2687G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr13:39446955 G>T maps to NM_207361.4 G2687G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr13:99364805 A>G maps to NM_005073.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr13:99364805 A>G maps to NM_005073.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr13:110814631 G>A maps to NM_001845.4 H1469H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr13:110814631 G>A maps to NM_001845.4 H1469H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr15:48434436 C>T maps to NM_205850.2 D464D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr15:48434436 C>T maps to NM_205850.2 D464D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr15:48818390 G>A maps to NM_000138.4 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr15:48818390 G>A maps to NM_000138.4 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr16:28917493 G>A maps to NM_024816.2 C423C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr16:28917493 G>A maps to NM_024816.2 C423C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr16:31105903 G>A maps to ENST00000319788 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr16:31105903 G>A maps to ENST00000319788 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr16:66603836 A>T did not map to a codon.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr16:66603836 A>T did not map to a codon.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr17:10351338 G>A maps to NM_017533.2 L1587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr17:10351338 G>A maps to NM_017533.2 L1587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr17:34266464 G>T did not map to a codon.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr17:34266464 G>T did not map to a codon.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr18:67614186 G>A maps to NM_006566.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr18:67614186 G>A maps to NM_006566.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:5598875 C>G maps to NM_014649.2 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:5598875 C>G maps to NM_014649.2 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:9577561 G>A maps to NM_152476.2 N687N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:9577561 G>A maps to NM_152476.2 N687N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:10221510 C>T maps to NM_001040664.2 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:10221510 C>T maps to NM_001040664.2 F390F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:44680225 C>T maps to NM_001032372.1 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:44680225 C>T maps to NM_001032372.1 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:44778657 G>T maps to NM_181756.1 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:44778657 G>T maps to NM_181756.1 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:55396679 C>A maps to NM_002000.2 S35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:55396679 C>A maps to NM_002000.2 S35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:57646306 C>T maps to NM_052882.1 Q466Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:57646306 C>T maps to NM_052882.1 Q466Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:58265187 C>A maps to NM_173632.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr19:58265187 C>A maps to NM_173632.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr2:143913202 T>C maps to NM_018460.3 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr2:143913202 T>C maps to NM_018460.3 D48D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr2:165986509 G>T maps to NM_006922.3 V954V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr2:165986509 G>T maps to NM_006922.3 V954V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr2:201468753 C>G maps to NM_001159.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr2:201468753 C>G maps to NM_001159.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr21:45076540 T>A maps to NM_007031.1 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr21:45076540 T>A maps to NM_007031.1 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr3:51400016 G>A maps to NM_004947.4 S1735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr3:51400016 G>A maps to NM_004947.4 S1735S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CV-6935-01A-11D-1912-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-CV-6935-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr4:65147242 G>A maps to NM_001010874.4 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr4:65147242 G>A maps to NM_001010874.4 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr5:13719183 G>T maps to NM_001369.2 C4102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr5:13719183 G>T maps to NM_001369.2 C4102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr5:66429470 A>G maps to NM_001164664.1 K741K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr5:66429470 A>G maps to NM_001164664.1 K741K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr5:140797509 G>T maps to NM_018927.2 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr5:140797509 G>T maps to NM_018927.2 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr5:168006279 G>A maps to NM_024594.2 I3I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr5:168006279 G>A maps to NM_024594.2 I3I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr6:26597371 G>T maps to NM_013375.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr6:26597371 G>T maps to NM_013375.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr6:41029193 C>A maps to NM_006789.3 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr6:41029193 C>A maps to NM_006789.3 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr6:70856591 A>T maps to NM_001858.4 P604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr6:70856591 A>T maps to NM_001858.4 P604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr6:132061453 C>T maps to NM_005021.3 C797C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr6:132061453 C>T maps to NM_005021.3 C797C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr7:23827672 A>G maps to NM_031414.3 S854S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr7:23827672 A>G maps to NM_031414.3 S854S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr7:23871840 C>T maps to NM_031414.3 F972F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr7:23871840 C>T maps to NM_031414.3 F972F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr7:33397535 C>A maps to NM_198428.2 S541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr7:33397535 C>A maps to NM_198428.2 S541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr7:88847531 G>T maps to NM_181646.2 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr7:88847531 G>T maps to NM_181646.2 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr8:72754901 G>T maps to NM_005098.3 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr8:72754901 G>T maps to NM_005098.3 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr8:95174379 G>T maps to NM_001144663.1 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr8:95174379 G>T maps to NM_001144663.1 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr8:139151250 G>C maps to NM_015912.3 L1293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr8:139151250 G>C maps to NM_015912.3 L1293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr8:143994843 C>A maps to NM_000498.3 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr8:143994843 C>A maps to NM_000498.3 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr8:144658322 C>A maps to ENST00000276844 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr8:144658322 C>A maps to ENST00000276844 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr9:19316462 G>T maps to NM_017925.4 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr9:19316462 G>T maps to NM_017925.4 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr9:125315510 G>C maps to NM_001004457.1 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr9:125315510 G>C maps to NM_001004457.1 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr9:139754407 G>A maps to ENST00000392881 V1171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr9:139754407 G>A maps to ENST00000392881 V1171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chrX:44938389 G>C did not map to a codon.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chrX:44938389 G>C did not map to a codon.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chrX:110924493 C>T maps to NM_001099922.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chrX:110924493 C>T maps to NM_001099922.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr15:22332431 C>T did not map to a codon.
Sequencing variant TCGA-CV-6935-01A-11D-1912-08 chr15:22332431 C>T did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:978799 C>T maps to NM_198576.2 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:978799 C>T maps to NM_198576.2 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:17662721 G>A did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:17662721 G>A did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:19204080 G>A maps to NM_003748.3 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:19204080 G>A maps to NM_003748.3 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:25810759 G>A maps to NM_018202.4 Q436Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:25810759 G>A maps to NM_018202.4 Q436Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:151237664 C>G maps to ENST00000368881 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:151237664 C>G maps to ENST00000368881 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:152327480 A>G maps to NM_001014342.2 S927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:152327480 A>G maps to NM_001014342.2 S927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:154898881 G>A maps to NM_006556.3 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:154898881 G>A maps to NM_006556.3 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:179562646 G>A maps to ENST00000444136 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:179562646 G>A maps to ENST00000444136 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:196920099 G>A maps to ENST00000367421 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:196920099 G>A maps to ENST00000367421 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:197298068 G>A maps to NM_201253.2 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:197298068 G>A maps to NM_201253.2 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:203186207 G>A maps to NM_003465.2 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:203186207 G>A maps to NM_003465.2 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:207741205 G>A maps to NM_000651.4 G1330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:207741205 G>A maps to NM_000651.4 G1330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:228432255 C>T maps to NM_001098623.1 F1155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:228432255 C>T maps to NM_001098623.1 F1155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:228556502 A>G maps to NM_001098623.1 P6616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:228556502 A>G maps to NM_001098623.1 P6616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr10:29599072 C>T maps to NM_032517.4 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr10:29599072 C>T maps to NM_032517.4 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr10:82187155 C>G maps to NM_032333.4 Y160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr10:82187155 C>G maps to NM_032333.4 Y160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr11:73106302 G>A maps to NM_152222.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr11:73106302 G>A maps to NM_152222.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr11:92918981 T>A did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr11:92918981 T>A did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr12:51851324 T>C did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr12:51851324 T>C did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr12:52201212 G>C maps to NM_014191.2 *1981Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr12:52201212 G>C maps to NM_014191.2 *1981Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr12:102036247 G>A maps to NM_002465.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr12:102036247 G>A maps to NM_002465.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr13:20763384 C>T maps to NM_004004.5 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr13:20763384 C>T maps to NM_004004.5 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr13:32869542 C>A maps to NM_023037.2 Y2996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr13:32869542 C>A maps to NM_023037.2 Y2996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr13:60544171 A>T maps to NM_001042517.1 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr13:60544171 A>T maps to NM_001042517.1 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr14:20216404 C>A maps to NM_172194.1 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr14:20216404 C>A maps to NM_172194.1 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr14:35593230 A>C maps to NM_014672.2 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr14:35593230 A>C maps to NM_014672.2 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr14:96757160 T>C maps to NM_018036.5 L1897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr14:96757160 T>C maps to NM_018036.5 L1897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr16:81087677 A>G maps to NM_001100873.1 *389Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr16:81087677 A>G maps to NM_001100873.1 *389Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr16:88664700 C>T maps to ENST00000452588 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr16:88664700 C>T maps to ENST00000452588 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr17:7230538 C>T maps to NM_032442.2 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr17:7230538 C>T maps to NM_032442.2 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr17:7752017 C>G maps to NM_001080424.1 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr17:7752017 C>G maps to NM_001080424.1 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr17:11607548 G>A maps to NM_001372.3 W1727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr17:11607548 G>A maps to NM_001372.3 W1727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr17:18775923 G>T maps to NM_002767.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr17:18775923 G>T maps to NM_002767.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr17:38938472 G>C maps to NM_181537.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr17:38938472 G>C maps to NM_181537.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr18:64178907 G>A maps to NM_021153.2 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr18:64178907 G>A maps to NM_021153.2 I491I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr19:4282868 G>A maps to NM_020209.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr19:4282868 G>A maps to NM_020209.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr19:8367859 G>A maps to NM_016579.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr19:8367859 G>A maps to NM_016579.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr19:12969219 C>T maps to NM_014975.2 F374F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr19:12969219 C>T maps to NM_014975.2 F374F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr19:46328446 C>G maps to NM_004819.2 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr19:46328446 C>G maps to NM_004819.2 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr2:66775127 C>T maps to ENST00000407092 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr2:66775127 C>T maps to ENST00000407092 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr2:70188033 G>A maps to NM_152792.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr2:70188033 G>A maps to NM_152792.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr2:149227842 C>T maps to ENST00000404807 N777N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr2:149227842 C>T maps to ENST00000404807 N777N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr2:168102260 T>G maps to NM_152381.5 T1453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr2:168102260 T>G maps to NM_152381.5 T1453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr2:190719575 T>C maps to NM_000534.4 C526C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr2:190719575 T>C maps to NM_000534.4 C526C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr2:231112643 C>T maps to NM_007237.4 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr2:231112643 C>T maps to NM_007237.4 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr2:237075003 C>A maps to NM_001485.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr2:237075003 C>A maps to NM_001485.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr20:30729429 C>T maps to NM_014742.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr20:30729429 C>T maps to NM_014742.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr20:33329652 T>C maps to NM_014071.2 K1469K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr20:33329652 T>C maps to NM_014071.2 K1469K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr21:28338236 G>A maps to NM_007038.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr21:28338236 G>A maps to NM_007038.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr21:46951983 G>A maps to NM_194255.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr21:46951983 G>A maps to NM_194255.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr22:19183839 G>A maps to NM_007098.3 L1376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr22:19183839 G>A maps to NM_007098.3 L1376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr22:19766782 G>A maps to NM_080646.1 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr22:19766782 G>A maps to NM_080646.1 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr22:21157490 G>A maps to NM_058004.2 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr22:21157490 G>A maps to NM_058004.2 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr22:21377466 C>T maps to NM_005446.3 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr22:21377466 C>T maps to NM_005446.3 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr22:26343754 G>C maps to ENST00000407587 L1905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr22:26343754 G>C maps to ENST00000407587 L1905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr22:27026340 C>T maps to NM_001886.2 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr22:27026340 C>T maps to NM_001886.2 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:3888389 G>T maps to NM_020873.5 E689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:3888389 G>T maps to NM_020873.5 E689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:15609958 C>T maps to NM_012260.2 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:15609958 C>T maps to NM_012260.2 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:30713697 C>T maps to NM_001024847.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:30713697 C>T maps to NM_001024847.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:37048547 G>A maps to NM_000249.3 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:37048547 G>A maps to NM_000249.3 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:52947575 G>C maps to NM_016329.3 S513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:52947575 G>C maps to NM_016329.3 S513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:55984514 G>A maps to ENST00000460849 Q781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:55984514 G>A maps to ENST00000460849 Q781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:121414935 T>C maps to ENST00000393667 E1478E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:121414935 T>C maps to ENST00000393667 E1478E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:136573800 C>T maps to NM_025246.2 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:136573800 C>T maps to NM_025246.2 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:157146113 G>A maps to NM_001167912.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr3:157146113 G>A maps to NM_001167912.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr4:41984114 C>T maps to NM_001029955.3 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr4:41984114 C>T maps to NM_001029955.3 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr4:42403209 C>G maps to NM_001080505.1 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr4:42403209 C>G maps to NM_001080505.1 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr4:175414435 C>T maps to NM_000860.4 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr4:175414435 C>T maps to NM_000860.4 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr4:175897134 C>T maps to NM_014269.4 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr4:175897134 C>T maps to NM_014269.4 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr4:186318368 G>A maps to NM_181726.2 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr4:186318368 G>A maps to NM_181726.2 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:53814495 C>T maps to NM_052870.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:53814495 C>T maps to NM_052870.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:79854711 G>C maps to NM_001004441.2 S376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:79854711 G>C maps to NM_001004441.2 S376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:94842672 G>A maps to NM_014639.3 Y1019Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:94842672 G>A maps to NM_014639.3 Y1019Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:140433130 C>A maps to NM_013340.2 V692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:140433130 C>A maps to NM_013340.2 V692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:140746179 G>A maps to NM_018918.2 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:140746179 G>A maps to NM_018918.2 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:140789448 G>A maps to NM_018926.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:140789448 G>A maps to NM_018926.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:151052774 T>C maps to NM_003118.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:151052774 T>C maps to NM_003118.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:176308466 G>A maps to NM_002115.2 D821D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr5:176308466 G>A maps to NM_002115.2 D821D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr6:29407890 C>T maps to NM_013941.2 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr6:29407890 C>T maps to NM_013941.2 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr6:32007954 C>T maps to NM_000500.5 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr6:32007954 C>T maps to NM_000500.5 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr6:41900356 C>T maps to NM_004053.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr6:41900356 C>T maps to NM_004053.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr6:146720757 C>T maps to NM_000838.3 G861G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr6:146720757 C>T maps to NM_000838.3 G861G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr7:37956079 G>A maps to ENST00000223214 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr7:37956079 G>A maps to ENST00000223214 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr7:108524577 C>G maps to NM_001024607.1 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr7:108524577 C>G maps to NM_001024607.1 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr7:138603486 G>A maps to NM_001164665.1 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr7:138603486 G>A maps to NM_001164665.1 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr7:139727112 G>A maps to NM_022750.2 R531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr7:139727112 G>A maps to NM_022750.2 R531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr8:28974434 G>A maps to NM_015254.3 I1250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr8:28974434 G>A maps to NM_015254.3 I1250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr8:77775693 T>C maps to NM_024721.4 N3248N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr8:77775693 T>C maps to NM_024721.4 N3248N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr8:87738775 C>T maps to NM_019098.4 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr8:87738775 C>T maps to NM_019098.4 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr8:135612759 C>T maps to NM_020863.3 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr8:135612759 C>T maps to NM_020863.3 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr9:15469057 T>C did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr9:15469057 T>C did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr9:136253247 C>G maps to NM_153710.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr9:136253247 C>G maps to NM_153710.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr9:139840947 G>C maps to NM_000606.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr9:139840947 G>C maps to NM_000606.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chrX:1554651 C>T did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chrX:1554651 C>T did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chrX:21545079 C>T maps to NM_014927.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chrX:21545079 C>T maps to NM_014927.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chrX:47074276 C>T maps to NM_153280.2 D1042D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chrX:47074276 C>T maps to NM_153280.2 D1042D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chrX:102842016 C>T maps to ENST00000372629 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chrX:102842016 C>T maps to ENST00000372629 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chrX:103041525 C>T maps to NM_000533.3 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chrX:103041525 C>T maps to NM_000533.3 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chrX:105280473 G>A maps to NM_000354.5 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chrX:105280473 G>A maps to NM_000354.5 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chrX:109922600 C>T maps to NM_001143981.1 E403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chrX:109922600 C>T maps to NM_001143981.1 E403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chrX:132548981 G>A maps to NM_001448.2 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chrX:132548981 G>A maps to NM_001448.2 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:228521392 C>T maps to NM_001098623.1 S5322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:228521392 C>T maps to NM_001098623.1 S5322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr4:109895697 T>C maps to ENST00000333642 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr4:109895697 T>C maps to ENST00000333642 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr1:12854333 C>G maps to NM_023013.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr1:12854333 C>G maps to NM_023013.2 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr1:77558067 G>A maps to NM_005482.2 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr1:77558067 G>A maps to NM_005482.2 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr1:157666097 C>T maps to NM_052939.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr1:157666097 C>T maps to NM_052939.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr1:160001163 G>A maps to NM_145167.2 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr1:160001163 G>A maps to NM_145167.2 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr1:200944710 G>A maps to NM_017596.2 L1497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr1:200944710 G>A maps to NM_017596.2 L1497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr1:209949071 C>A maps to NM_025228.2 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr1:209949071 C>A maps to NM_025228.2 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr11:7111301 T>C maps to NM_014469.4 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr11:7111301 T>C maps to NM_014469.4 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr11:56431505 G>C maps to NM_001004730.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr11:56431505 G>C maps to NM_001004730.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr12:4919816 C>T maps to NM_002235.3 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr12:4919816 C>T maps to NM_002235.3 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr14:71444808 T>A maps to NM_014982.2 G585G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr14:71444808 T>A maps to NM_014982.2 G585G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr14:95571505 T>A maps to NM_177438.2 I1057I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr14:95571505 T>A maps to NM_177438.2 I1057I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr17:8793323 C>T maps to NM_001142633.1 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr17:8793323 C>T maps to NM_001142633.1 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr19:36037695 G>A maps to NM_032635.2 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr19:36037695 G>A maps to NM_032635.2 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr19:47570689 G>A maps to NM_015168.1 P945P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr19:47570689 G>A maps to NM_015168.1 P945P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr2:1648499 G>A maps to NM_012293.1 I1211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr2:1648499 G>A maps to NM_012293.1 I1211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr2:80530509 C>T maps to NM_178839.4 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr2:80530509 C>T maps to NM_178839.4 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr20:40710551 A>G maps to ENST00000373198 R1436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr20:40710551 A>G maps to ENST00000373198 R1436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr22:21134278 C>T maps to NM_000185.3 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr22:21134278 C>T maps to NM_000185.3 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr22:21134358 C>T maps to NM_000185.3 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr22:21134358 C>T maps to NM_000185.3 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr22:21134469 C>T maps to NM_000185.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr22:21134469 C>T maps to NM_000185.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr22:21134478 C>T maps to NM_000185.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr22:21134478 C>T maps to NM_000185.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr22:24582116 G>A maps to NM_019601.3 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr22:24582116 G>A maps to NM_019601.3 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr3:119459394 G>T did not map to a codon.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr3:119459394 G>T did not map to a codon.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr3:196753555 C>T maps to NM_005929.5 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr3:196753555 C>T maps to NM_005929.5 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr4:8472842 C>T maps to NM_152544.2 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr4:8472842 C>T maps to NM_152544.2 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr4:13603426 T>C maps to NM_148894.2 A1699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr4:13603426 T>C maps to NM_148894.2 A1699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr4:70346486 G>A maps to NM_021139.2 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr4:70346486 G>A maps to NM_021139.2 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr4:114257134 G>A maps to NM_001148.4 L1171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr4:114257134 G>A maps to NM_001148.4 L1171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr5:113740538 C>T maps to NM_021614.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr5:113740538 C>T maps to NM_021614.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr5:140263295 C>T maps to NM_018904.2 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr5:140263295 C>T maps to NM_018904.2 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr5:161324317 C>T maps to NM_001127648.1 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr5:161324317 C>T maps to NM_001127648.1 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr6:29911171 G>A maps to ENST00000376806 W157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr6:29911171 G>A maps to ENST00000376806 W157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr6:33703226 G>A maps to NM_054111.4 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr6:33703226 G>A maps to NM_054111.4 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr6:110636639 A>G maps to NM_001123364.1 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr6:110636639 A>G maps to NM_001123364.1 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr6:149944271 T>C maps to NM_007044.2 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr6:149944271 T>C maps to NM_007044.2 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr7:55242488 G>A maps to NM_005228.3 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr7:55242488 G>A maps to NM_005228.3 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr7:100463758 C>A maps to NM_020246.2 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr7:100463758 C>A maps to NM_020246.2 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr7:103270582 C>A maps to ENST00000428762 G836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr7:103270582 C>A maps to ENST00000428762 G836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr8:134030137 C>T maps to NM_003235.4 D2226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr8:134030137 C>T maps to NM_003235.4 D2226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr9:101980620 C>T maps to NM_033087.3 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr9:101980620 C>T maps to NM_033087.3 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr9:126414315 G>A maps to NM_020946.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr9:126414315 G>A maps to NM_020946.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr9:133506174 C>T maps to NM_003934.1 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr9:133506174 C>T maps to NM_003934.1 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chrX:12937992 A>T maps to ENST00000311912 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chrX:12937992 A>T maps to ENST00000311912 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chrX:62917121 G>T maps to NM_015185.2 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chrX:62917121 G>T maps to NM_015185.2 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr1:9022704 C>T maps to ENST00000413627 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr1:9022704 C>T maps to ENST00000413627 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr1:152083256 C>T maps to NM_007113.2 P812P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr1:152083256 C>T maps to NM_007113.2 P812P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr1:155029697 C>T maps to NM_207197.1 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr1:155029697 C>T maps to NM_207197.1 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr1:156206090 G>T maps to NM_007221.3 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr1:156206090 G>T maps to NM_007221.3 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr1:161953755 C>T maps to ENST00000451379 A655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr1:161953755 C>T maps to ENST00000451379 A655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr1:209969691 C>G did not map to a codon.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr1:209969691 C>G did not map to a codon.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr1:230841941 C>T maps to NM_000029.3 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr1:230841941 C>T maps to NM_000029.3 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr10:22606901 C>T maps to NM_012071.2 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr10:22606901 C>T maps to NM_012071.2 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr10:72489915 G>A maps to NM_139155.2 W338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr10:72489915 G>A maps to NM_139155.2 W338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr11:5758255 G>T maps to NM_001005180.2 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr11:5758255 G>T maps to NM_001005180.2 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr11:65319551 G>A maps to NM_001130144.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr11:65319551 G>A maps to NM_001130144.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr11:124487351 C>T maps to NM_052959.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr11:124487351 C>T maps to NM_052959.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr12:44148514 G>A maps to NM_031292.3 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr12:44148514 G>A maps to NM_031292.3 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr12:56221561 C>T maps to NM_032364.5 W294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr12:56221561 C>T maps to NM_032364.5 W294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr12:122012497 C>T maps to ENST00000377071 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr12:122012497 C>T maps to ENST00000377071 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr13:46627850 G>A maps to NM_001872.3 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr13:46627850 G>A maps to NM_001872.3 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr14:76452139 T>A maps to NM_052873.2 L4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr14:76452139 T>A maps to NM_052873.2 L4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr15:57565365 T>A maps to NM_207036.1 C628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr15:57565365 T>A maps to NM_207036.1 C628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr15:101719014 A>G maps to NM_014918.4 H329H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr15:101719014 A>G maps to NM_014918.4 H329H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr16:3296523 C>T did not map to a codon.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr16:3296523 C>T did not map to a codon.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr16:10524588 C>T maps to NM_024997.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr16:10524588 C>T maps to NM_024997.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr16:20990732 C>G maps to NM_017539.1 L2665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr16:20990732 C>G maps to NM_017539.1 L2665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr16:31477645 C>T maps to ENST00000408912 P843P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr16:31477645 C>T maps to ENST00000408912 P843P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr16:50347891 C>T maps to NM_001114.3 S925S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr16:50347891 C>T maps to NM_001114.3 S925S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr16:67670669 C>T maps to NM_006565.3 Q639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr16:67670669 C>T maps to NM_006565.3 Q639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr16:76482787 C>T maps to NM_033401.3 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr16:76482787 C>T maps to NM_033401.3 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr17:26901250 A>G maps to NM_005165.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr17:26901250 A>G maps to NM_005165.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr20:62197117 C>T maps to NM_001037335.2 T1019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr20:62197117 C>T maps to NM_001037335.2 T1019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr22:20127071 C>T maps to NM_013373.3 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr22:20127071 C>T maps to NM_013373.3 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr22:24583659 C>G maps to NM_019601.3 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr22:24583659 C>G maps to NM_019601.3 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr22:24953662 T>A maps to NM_004175.3 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr22:24953662 T>A maps to NM_004175.3 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr3:41275707 C>T maps to NM_001904.3 R535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr3:41275707 C>T maps to NM_001904.3 R535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr3:122642481 G>A maps to NM_001031702.2 N418N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr3:122642481 G>A maps to NM_001031702.2 N418N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr4:8305955 C>G maps to NM_053044.3 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr4:8305955 C>G maps to NM_053044.3 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr4:71510265 G>A maps to NM_031889.2 E1041E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr4:71510265 G>A maps to NM_031889.2 E1041E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr4:76721830 A>C maps to NM_003715.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr4:76721830 A>C maps to NM_003715.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr4:187524189 T>C did not map to a codon.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr4:187524189 T>C did not map to a codon.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr5:131396410 G>T maps to NM_000588.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr5:131396410 G>T maps to NM_000588.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr5:140250226 C>T maps to NM_018902.3 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr5:140250226 C>T maps to NM_018902.3 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr6:17669741 G>C maps to ENST00000430136 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr6:17669741 G>C maps to ENST00000430136 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr6:117050815 T>C maps to NM_002269.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr6:117050815 T>C maps to NM_002269.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr7:143088617 G>A maps to NM_005232.4 Q955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr7:143088617 G>A maps to NM_005232.4 Q955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr8:24333984 C>T maps to ENST00000380789 R225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr8:24333984 C>T maps to ENST00000380789 R225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr8:48733338 G>A maps to NM_006904.6 Q3092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr8:48733338 G>A maps to NM_006904.6 Q3092*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chrX:117043396 G>C maps to NM_033495.3 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chrX:117043396 G>C maps to NM_033495.3 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chrX:153689701 C>T maps to NM_017514.3 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chrX:153689701 C>T maps to NM_017514.3 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr10:102988335 G>C maps to NM_006562.4 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6938-01A-11D-1912-08 chr10:102988335 G>C maps to NM_006562.4 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr1:10725437 A>T maps to NM_001079843.1 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr1:10725437 A>T maps to NM_001079843.1 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr1:101490908 G>A maps to NM_015958.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr1:101490908 G>A maps to NM_015958.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr1:192778227 T>C maps to NM_002923.3 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr1:192778227 T>C maps to NM_002923.3 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr10:135195044 C>A maps to NM_152911.2 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr10:135195044 C>A maps to NM_152911.2 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr11:71725191 G>A maps to ENST00000393695 G1125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr11:71725191 G>A maps to ENST00000393695 G1125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr13:99340611 T>C did not map to a codon.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr13:99340611 T>C did not map to a codon.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr14:103363737 G>A maps to NM_145725.2 Q320Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr14:103363737 G>A maps to NM_145725.2 Q320Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr16:67335718 G>C maps to NM_001100915.1 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr16:67335718 G>C maps to NM_001100915.1 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr18:64172338 C>A maps to NM_021153.2 E677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr18:64172338 C>A maps to NM_021153.2 E677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr19:44981989 A>G maps to NM_013256.3 H236H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr19:44981989 A>G maps to NM_013256.3 H236H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr20:13856746 C>A maps to NM_025229.1 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr20:13856746 C>A maps to NM_025229.1 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr3:130452854 G>C maps to NM_014602.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr3:130452854 G>C maps to NM_014602.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr3:142985668 G>A maps to NM_173653.3 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr3:142985668 G>A maps to NM_173653.3 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr5:154296702 C>T maps to NM_015465.3 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr5:154296702 C>T maps to NM_015465.3 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr8:73921393 C>T maps to NM_017489.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr8:73921393 C>T maps to NM_017489.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr9:137801844 G>A maps to NM_002003.3 D260D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr9:137801844 G>A maps to NM_002003.3 D260D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chrX:70339728 T>G did not map to a codon.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chrX:70339728 T>G did not map to a codon.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr19:58386283 T>C maps to NM_001144989.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6939-01A-11D-1912-08 chr19:58386283 T>C maps to NM_001144989.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr1:6697513 G>A maps to NM_018198.3 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr1:6697513 G>A maps to NM_018198.3 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr1:70819808 G>A maps to NM_030816.4 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr1:70819808 G>A maps to NM_030816.4 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr1:102312415 C>A maps to ENST00000338858 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr1:102312415 C>A maps to ENST00000338858 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr1:145368629 G>A maps to NM_001039703.4 L3536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr1:145368629 G>A maps to NM_001039703.4 L3536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr1:152383332 C>T maps to NM_016190.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr1:152383332 C>T maps to NM_016190.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr11:51516006 C>T maps to NM_001004703.1 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr11:51516006 C>T maps to NM_001004703.1 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr11:71148917 G>A maps to NM_001360.2 H301H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr11:71148917 G>A maps to NM_001360.2 H301H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr12:52912853 C>A maps to NM_000424.3 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr12:52912853 C>A maps to NM_000424.3 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr12:124107221 G>A maps to NM_001414.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr12:124107221 G>A maps to NM_001414.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr13:36050071 G>A maps to NM_005584.4 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr13:36050071 G>A maps to NM_005584.4 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr13:50123785 T>C did not map to a codon.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr13:50123785 T>C did not map to a codon.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr13:100982840 C>T maps to NM_000282.3 R486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr13:100982840 C>T maps to NM_000282.3 R486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr15:34380294 G>A maps to NM_020154.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr15:34380294 G>A maps to NM_020154.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr15:42132976 C>T maps to NM_005090.3 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr15:42132976 C>T maps to NM_005090.3 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr15:42133452 C>T maps to NM_005090.3 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr15:42133452 C>T maps to NM_005090.3 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr15:42134774 G>A maps to NM_005090.3 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr15:42134774 G>A maps to NM_005090.3 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr15:45408912 C>T maps to NM_207581.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr15:45408912 C>T maps to NM_207581.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr15:102462359 A>G maps to NM_001004195.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr15:102462359 A>G maps to NM_001004195.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr16:48382182 G>C maps to NM_031490.2 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr16:48382182 G>C maps to NM_031490.2 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr17:10296299 C>A maps to NM_002472.2 E1771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr17:10296299 C>A maps to NM_002472.2 E1771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr17:26960317 G>A maps to NM_014680.2 N1189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr17:26960317 G>A maps to NM_014680.2 N1189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr17:36482451 C>A maps to ENST00000398597 E2335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr17:36482451 C>A maps to ENST00000398597 E2335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr17:61571741 C>G maps to NM_000789.3 Y1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr17:61571741 C>G maps to NM_000789.3 Y1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr19:14512332 C>T maps to NM_078481.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr19:14512332 C>T maps to NM_078481.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr19:42383228 G>A maps to NM_001783.3 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr19:42383228 G>A maps to NM_001783.3 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr2:18112571 C>T maps to NM_002252.3 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr2:18112571 C>T maps to NM_002252.3 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr2:18113211 C>T maps to NM_002252.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr2:18113211 C>T maps to NM_002252.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr2:75347731 C>T maps to NM_001058.3 W184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr2:75347731 C>T maps to NM_001058.3 W184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr2:220078865 G>A maps to NM_005689.2 R477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr2:220078865 G>A maps to NM_005689.2 R477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr20:139649 G>A maps to NM_139074.2 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr20:139649 G>A maps to NM_139074.2 K95K. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CV-6940-01A-11D-1912-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CV-6940-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr22:36657699 G>A maps to NM_145343.2 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr22:36657699 G>A maps to NM_145343.2 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr3:121340737 T>C maps to NM_016298.3 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr3:121340737 T>C maps to NM_016298.3 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr4:48036924 C>T maps to NM_207330.1 N163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr4:48036924 C>T maps to NM_207330.1 N163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr4:48172262 A>C did not map to a codon.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr4:48172262 A>C did not map to a codon.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr4:100534245 C>T maps to ENST00000511045 G749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr4:100534245 C>T maps to ENST00000511045 G749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr4:166231783 C>T maps to NM_001161521.1 Y377Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr4:166231783 C>T maps to NM_001161521.1 Y377Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr4:167675843 G>C maps to NM_016950.2 S252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr4:167675843 G>C maps to NM_016950.2 S252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr6:90434919 G>A maps to NM_014611.1 Q1890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr6:90434919 G>A maps to NM_014611.1 Q1890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr6:151672231 A>G maps to NM_005100.3 A902A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr6:151672231 A>G maps to NM_005100.3 A902A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr7:23830530 C>G maps to NM_031414.3 S909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr7:23830530 C>G maps to NM_031414.3 S909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr7:75172194 G>A maps to NM_005338.4 S955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr7:75172194 G>A maps to NM_005338.4 S955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr7:93055849 G>A maps to NM_001164737.1 Q449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr7:93055849 G>A maps to NM_001164737.1 Q449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr7:99773452 G>A maps to NM_152742.1 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr7:99773452 G>A maps to NM_152742.1 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr7:141619409 C>T maps to NM_001001656.1 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr7:141619409 C>T maps to NM_001001656.1 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr8:25346198 G>A maps to ENST00000434814 K556K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr8:25346198 G>A maps to ENST00000434814 K556K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr8:87423944 A>G maps to NM_007013.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr8:87423944 A>G maps to NM_007013.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr8:102585905 C>T maps to NM_024915.3 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr8:102585905 C>T maps to NM_024915.3 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr8:107773699 C>T maps to NM_139166.4 Q237Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr8:107773699 C>T maps to NM_139166.4 Q237Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr9:117483 G>T maps to NM_207305.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr9:117483 G>T maps to NM_207305.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr9:79824393 C>T maps to ENST00000376646 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr9:79824393 C>T maps to ENST00000376646 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr9:98218641 G>A maps to NM_000264.3 I1074I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr9:98218641 G>A maps to NM_000264.3 I1074I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chrX:105011443 T>C maps to NM_017416.1 C617C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chrX:105011443 T>C maps to NM_017416.1 C617C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr1:23385656 A>G maps to NM_001009999.2 Q388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr1:23385656 A>G maps to NM_001009999.2 Q388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr1:50666795 G>T maps to NM_021952.3 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr1:50666795 G>T maps to NM_021952.3 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr1:68947900 A>C maps to NM_001114120.1 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr1:68947900 A>C maps to NM_001114120.1 A530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr1:103345448 T>C maps to NM_080629.2 G1700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr1:103345448 T>C maps to NM_080629.2 G1700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr1:166927306 G>A maps to NM_199351.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr1:166927306 G>A maps to NM_199351.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr1:248685813 C>A maps to NM_001013355.1 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr1:248685813 C>A maps to NM_001013355.1 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr10:412283 C>G maps to NM_014974.2 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr10:412283 C>G maps to NM_014974.2 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr10:5789367 G>A maps to NM_017782.4 E1328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr10:5789367 G>A maps to NM_017782.4 E1328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr10:56287614 T>C maps to NM_001142763.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr10:56287614 T>C maps to NM_001142763.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr10:61832597 G>A maps to NM_020987.2 Q2681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr10:61832597 G>A maps to NM_020987.2 Q2681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr11:4703254 G>A maps to NM_030774.3 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr11:4703254 G>A maps to NM_030774.3 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr11:35496242 G>A maps to NM_015430.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr11:35496242 G>A maps to NM_015430.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr11:47739053 C>A maps to NM_015308.2 E992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr11:47739053 C>A maps to NM_015308.2 E992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr11:76891460 G>A maps to NM_000260.3 E876E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr11:76891460 G>A maps to NM_000260.3 E876E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr12:7548985 C>T maps to ENST00000416109 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr12:7548985 C>T maps to ENST00000416109 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr12:13828793 C>T did not map to a codon.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr12:13828793 C>T did not map to a codon.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr12:46321866 T>C maps to NM_004719.2 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr12:46321866 T>C maps to NM_004719.2 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr12:52992875 C>T maps to NM_080747.2 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr12:52992875 C>T maps to NM_080747.2 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr12:101510519 A>C maps to ENST00000392977 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr12:101510519 A>C maps to ENST00000392977 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr13:113200120 C>T maps to NM_006322.4 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr13:113200120 C>T maps to NM_006322.4 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr15:27572156 A>T maps to NM_033223.4 K158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr15:27572156 A>T maps to NM_033223.4 K158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr15:78472019 C>T maps to NM_015162.4 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr15:78472019 C>T maps to NM_015162.4 A452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr16:1035025 G>A maps to NM_014587.3 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr16:1035025 G>A maps to NM_014587.3 S327S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr16:3169974 C>T maps to NM_001042428.1 H438H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr16:3169974 C>T maps to NM_001042428.1 H438H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr16:89619493 C>T maps to NM_003119.2 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr16:89619493 C>T maps to NM_003119.2 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr17:18065897 G>T did not map to a codon.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr17:18065897 G>T did not map to a codon.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr17:34077221 T>A maps to NM_139285.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr17:34077221 T>A maps to NM_139285.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr17:56060237 G>A maps to NM_007146.2 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr17:56060237 G>A maps to NM_007146.2 R184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr17:77758171 G>A maps to NM_005189.2 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr17:77758171 G>A maps to NM_005189.2 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr18:33795645 C>T maps to NM_017947.2 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr18:33795645 C>T maps to NM_017947.2 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr19:312209 G>A maps to NM_017550.1 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr19:312209 G>A maps to NM_017550.1 F290F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr2:63283435 G>T maps to NM_014562.3 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr2:63283435 G>T maps to NM_014562.3 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr2:128712713 C>T maps to NM_001145928.1 A782A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr2:128712713 C>T maps to NM_001145928.1 A782A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr2:169690789 T>C maps to NM_001171631.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr2:169690789 T>C maps to NM_001171631.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr2:218674658 C>T maps to NM_022648.4 Q1616Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr2:218674658 C>T maps to NM_022648.4 Q1616Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr20:2315840 G>A maps to NM_003245.3 A574A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr20:2315840 G>A maps to NM_003245.3 A574A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr3:49329941 C>G did not map to a codon.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr3:49329941 C>G did not map to a codon.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr4:94031920 C>T maps to NM_001510.2 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr4:94031920 C>T maps to NM_001510.2 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr4:134072701 C>T maps to NM_032961.1 D469D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr4:134072701 C>T maps to NM_032961.1 D469D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr5:5237175 G>A maps to NM_139056.2 E706E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr5:5237175 G>A maps to NM_139056.2 E706E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr5:37480010 G>A maps to NM_018034.2 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr5:37480010 G>A maps to NM_018034.2 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr5:176673716 C>T maps to NM_022455.4 R1473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr5:176673716 C>T maps to NM_022455.4 R1473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr7:6045546 G>A maps to NM_000535.5 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr7:6045546 G>A maps to NM_000535.5 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr7:44739835 C>A maps to ENST00000444676 R858R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr7:44739835 C>A maps to ENST00000444676 R858R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr7:138738293 G>A maps to ENST00000464606 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr7:138738293 G>A maps to ENST00000464606 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr8:68130078 T>C maps to NM_006421.3 L1517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr8:68130078 T>C maps to NM_006421.3 L1517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr8:146033062 C>T maps to NM_213605.2 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr8:146033062 C>T maps to NM_213605.2 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr8:146157089 G>A maps to NM_006958.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr8:146157089 G>A maps to NM_006958.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr9:72723127 C>T maps to NM_153267.4 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr9:72723127 C>T maps to NM_153267.4 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr9:96051364 G>A maps to ENST00000297954 P1480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6941-01A-11D-1912-08 chr9:96051364 G>A maps to ENST00000297954 P1480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:12336510 C>T maps to NM_015378.2 L956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:12336510 C>T maps to NM_015378.2 L956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:39826463 G>C did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:39826463 G>C did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:44685130 C>G maps to NM_019100.4 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:44685130 C>G maps to NM_019100.4 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:47264770 C>T maps to NM_001099772.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:47264770 C>T maps to NM_001099772.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:52729529 C>G maps to NM_004799.2 S755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:52729529 C>G maps to NM_004799.2 S755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:95710025 C>A maps to NM_015485.4 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:95710025 C>A maps to NM_015485.4 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:97564047 G>T maps to NM_000110.3 I921I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:97564047 G>T maps to NM_000110.3 I921I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:149785050 C>G maps to NM_001123375.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:149785050 C>G maps to NM_001123375.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:160001445 G>A maps to NM_145167.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:160001445 G>A maps to NM_145167.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:203696680 G>A maps to NM_001001396.1 L1097L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:203696680 G>A maps to NM_001001396.1 L1097L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:213147382 C>T maps to NM_001136474.1 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr1:213147382 C>T maps to NM_001136474.1 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr10:45799189 C>T maps to NM_001004297.2 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr10:45799189 C>T maps to NM_001004297.2 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr11:34668199 C>G maps to NM_012153.4 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr11:34668199 C>G maps to NM_012153.4 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr11:49214403 C>A maps to NM_004476.1 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr11:49214403 C>A maps to NM_004476.1 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr11:57982299 G>T maps to NM_001004458.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr11:57982299 G>T maps to NM_001004458.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr12:113758154 G>A maps to NM_024959.2 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr12:113758154 G>A maps to NM_024959.2 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr13:42335295 G>C maps to NM_015058.1 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr13:42335295 G>C maps to NM_015058.1 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr14:21167748 C>T maps to NM_194431.1 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr14:21167748 C>T maps to NM_194431.1 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr14:70518745 G>T maps to NM_183002.1 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr14:70518745 G>T maps to NM_183002.1 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr14:73989499 G>A maps to ENST00000334988 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr14:73989499 G>A maps to ENST00000334988 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr15:31358387 G>A maps to NM_002420.4 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr15:31358387 G>A maps to NM_002420.4 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr15:41350927 G>A maps to NM_017553.1 Q632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr15:41350927 G>A maps to NM_017553.1 Q632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr15:63481933 C>T maps to NM_016530.2 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr15:63481933 C>T maps to NM_016530.2 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr15:65916744 G>A maps to NM_004727.2 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr15:65916744 G>A maps to NM_004727.2 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr15:65918076 C>T maps to NM_004727.2 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr15:65918076 C>T maps to NM_004727.2 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr16:67272350 C>T did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr16:67272350 C>T did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr17:3550807 C>T maps to NM_001031681.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr17:3550807 C>T maps to NM_001031681.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr17:7576854 G>A maps to NM_001126112.1 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr17:8790442 G>C maps to NM_001142633.1 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr17:8790442 G>C maps to NM_001142633.1 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr17:17061835 G>A maps to NM_015134.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr17:17061835 G>A maps to NM_015134.2 P522P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CV-6942-01A-21D-2012-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-CV-6942-01A-21D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr17:40557193 G>A maps to NM_012232.5 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr17:40557193 G>A maps to NM_012232.5 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr17:61910723 G>C maps to NM_001098426.1 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr17:61910723 G>C maps to NM_001098426.1 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr18:40853922 G>C maps to NM_020783.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr18:40853922 G>C maps to NM_020783.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr18:56897645 C>G maps to NM_002091.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr18:56897645 C>G maps to NM_002091.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr19:10254620 G>A maps to NM_001130823.1 P979P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr19:10254620 G>A maps to NM_001130823.1 P979P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr19:15061150 G>T maps to NM_005071.1 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr19:15061150 G>T maps to NM_005071.1 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr19:21300909 C>G maps to NM_182515.3 Y480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr19:21300909 C>G maps to NM_182515.3 Y480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr19:57746746 C>T maps to NM_001015878.1 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr19:57746746 C>T maps to NM_001015878.1 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr2:11284116 G>A maps to NM_182500.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr2:11284116 G>A maps to NM_182500.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr2:26688664 C>A maps to NM_194248.2 T1558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr2:26688664 C>A maps to NM_194248.2 T1558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr2:27360066 A>G maps to NM_178553.3 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr2:27360066 A>G maps to NM_178553.3 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr2:129025881 G>A maps to NM_004807.2 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr2:129025881 G>A maps to NM_004807.2 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr2:197767386 T>A maps to NM_024989.3 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr2:197767386 T>A maps to NM_024989.3 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr2:219000051 G>A maps to NM_001168298.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr2:219000051 G>A maps to NM_001168298.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr2:234527111 G>A maps to NM_019076.4 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr2:234527111 G>A maps to NM_019076.4 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr20:44675030 G>T maps to NM_001134771.1 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr20:44675030 G>T maps to NM_001134771.1 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr20:55750063 C>G did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr20:55750063 C>G did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr20:58349448 G>T maps to NM_080672.3 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr20:58349448 G>T maps to NM_080672.3 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr21:11049620 G>A maps to NM_182482.2 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr21:11049620 G>A maps to NM_182482.2 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr21:43531074 C>T maps to NM_173568.3 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr21:43531074 C>T maps to NM_173568.3 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr22:17288844 G>C maps to NM_175878.3 S40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr22:17288844 G>C maps to NM_175878.3 S40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr22:38690153 G>A maps to NM_001894.4 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr22:38690153 G>A maps to NM_001894.4 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr3:32612232 G>A maps to NM_016141.3 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr3:32612232 G>A maps to NM_016141.3 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr3:41266589 A>G maps to NM_001904.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr3:41266589 A>G maps to NM_001904.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr3:42229592 C>T maps to NM_001042646.1 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr3:42229592 C>T maps to NM_001042646.1 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr3:141292834 C>G maps to ENST00000452898 S470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr3:141292834 C>G maps to ENST00000452898 S470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr4:11400945 G>A maps to NM_005114.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr4:11400945 G>A maps to NM_005114.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr4:42416642 C>T did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr4:42416642 C>T did not map to a codon.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr4:151271209 C>G maps to NM_006726.3 V2443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr4:151271209 C>G maps to NM_006726.3 V2443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr5:56152465 C>T maps to NM_005921.1 H174H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr5:56152465 C>T maps to NM_005921.1 H174H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr5:74077285 C>G maps to NM_015566.1 *671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr5:74077285 C>G maps to NM_015566.1 *671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr5:74722219 A>T maps to NM_001130105.1 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr5:74722219 A>T maps to NM_001130105.1 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr5:140502281 C>A maps to NM_018938.2 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr5:140502281 C>A maps to NM_018938.2 I234I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr5:167419990 C>T maps to NM_001122679.1 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr5:167419990 C>T maps to NM_001122679.1 F330F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr6:29274828 C>T maps to NM_030946.1 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr6:29274828 C>T maps to NM_030946.1 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr6:31934520 C>T maps to NM_006929.4 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr6:31934520 C>T maps to NM_006929.4 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr6:31934893 G>C maps to NM_006929.4 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr6:31934893 G>C maps to NM_006929.4 L818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr6:47678615 C>G maps to NM_153838.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr6:47678615 C>G maps to NM_153838.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr6:135787270 C>A maps to NM_017651.4 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr6:135787270 C>A maps to NM_017651.4 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr7:24905838 G>A maps to NM_015550.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr7:24905838 G>A maps to NM_015550.2 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr7:48068469 G>A maps to NM_152782.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr7:48068469 G>A maps to NM_152782.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr7:72849296 C>G maps to NM_003508.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr7:72849296 C>G maps to NM_003508.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr7:72849452 C>T maps to NM_003508.2 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr7:72849452 C>T maps to NM_003508.2 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr7:82763967 T>C maps to NM_033026.5 Q966Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr7:82763967 T>C maps to NM_033026.5 Q966Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr7:123097515 G>T maps to NM_178827.4 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr7:123097515 G>T maps to NM_178827.4 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr7:152012252 G>C maps to ENST00000355193 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr7:152012252 G>C maps to ENST00000355193 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr8:95172203 T>A maps to NM_001144663.1 K516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr8:95172203 T>A maps to NM_001144663.1 K516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr9:90296351 C>T maps to NM_004938.2 R679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr9:90296351 C>T maps to NM_004938.2 R679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr9:91653162 G>T maps to NM_016848.5 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr9:91653162 G>T maps to NM_016848.5 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chrX:37586995 C>T maps to NM_021083.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chrX:37586995 C>T maps to NM_021083.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chrX:55757889 C>T maps to NM_016656.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chrX:55757889 C>T maps to NM_016656.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chrX:125299535 G>A maps to NM_001013628.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chrX:125299535 G>A maps to NM_001013628.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chrX:153178183 G>C maps to NM_001164741.1 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chrX:153178183 G>C maps to NM_001164741.1 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr1:8928110 C>G maps to NM_001428.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr1:8928110 C>G maps to NM_001428.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr11:3697544 A>G maps to NM_016320.4 D1749D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr11:3697544 A>G maps to NM_016320.4 D1749D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr11:65482117 C>T maps to NM_182710.1 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr11:65482117 C>T maps to NM_182710.1 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr12:48143716 G>A maps to NM_001098531.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr12:48143716 G>A maps to NM_001098531.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr14:20296392 C>T maps to NM_001004723.1 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr14:20296392 C>T maps to NM_001004723.1 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr14:30107996 C>T maps to NM_002742.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr14:30107996 C>T maps to NM_002742.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr17:26962165 C>A maps to NM_014680.2 R813R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr17:26962165 C>A maps to NM_014680.2 R813R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr17:33680114 T>A maps to NM_152270.3 R656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr17:33680114 T>A maps to NM_152270.3 R656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr17:76128899 G>T maps to NM_152468.4 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr17:76128899 G>T maps to NM_152468.4 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr19:12997870 G>A maps to NM_006563.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr19:12997870 G>A maps to NM_006563.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr19:48253510 C>G maps to NM_015710.4 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr19:48253510 C>G maps to NM_015710.4 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr3:30691946 C>G maps to NM_001024847.2 S175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr3:30691946 C>G maps to NM_001024847.2 S175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr3:51430467 G>A maps to NM_013286.4 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr3:51430467 G>A maps to NM_013286.4 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr4:187539416 G>A maps to ENST00000260147 Q2778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr4:187539416 G>A maps to ENST00000260147 Q2778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr6:28269232 C>G maps to NM_032507.3 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr6:28269232 C>G maps to NM_032507.3 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr6:29912174 G>T did not map to a codon.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr6:29912174 G>T did not map to a codon.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr6:157528757 C>T maps to ENST00000367148 S2201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr6:157528757 C>T maps to ENST00000367148 S2201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr7:38305121 C>G maps to ENST00000443402 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr7:38305121 C>G maps to ENST00000443402 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr8:2020521 C>G maps to NM_003970.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr8:2020521 C>G maps to NM_003970.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr8:104709389 C>T maps to NM_001100117.2 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr8:104709389 C>T maps to NM_001100117.2 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr9:33385822 G>A maps to NM_001170.1 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr9:33385822 G>A maps to NM_001170.1 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr9:140150357 G>C did not map to a codon.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chr9:140150357 G>C did not map to a codon.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chrX:13762638 G>T did not map to a codon.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chrX:13762638 G>T did not map to a codon.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chrX:100524181 C>T maps to NM_024885.3 *463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chrX:100524181 C>T maps to NM_024885.3 *463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chrX:109694738 C>G maps to NM_020769.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chrX:109694738 C>G maps to NM_020769.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chrX:150911101 C>T maps to NM_005140.1 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6943-01A-11D-1912-08 chrX:150911101 C>T maps to NM_005140.1 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr1:52305984 T>C maps to NM_002525.2 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr1:52305984 T>C maps to NM_002525.2 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr1:156518470 A>T maps to NM_178229.4 L632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr1:156518470 A>T maps to NM_178229.4 L632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr1:159842918 C>T maps to NM_012337.2 E464E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr1:159842918 C>T maps to NM_012337.2 E464E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr10:16918893 A>T did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr10:16918893 A>T did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr10:96162459 G>A maps to NM_015188.1 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr10:96162459 G>A maps to NM_015188.1 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr10:134014378 C>T maps to NM_006426.2 C334C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr10:134014378 C>T maps to NM_006426.2 C334C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr11:59190240 G>A maps to NM_001001954.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr11:59190240 G>A maps to NM_001001954.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr11:66192685 G>A maps to NM_178864.3 G775G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr11:66192685 G>A maps to NM_178864.3 G775G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr11:134253870 C>T maps to NM_054025.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr11:134253870 C>T maps to NM_054025.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr12:7046364 C>G maps to NM_001940.3 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr12:7046364 C>G maps to NM_001940.3 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr12:51853841 G>T maps to NM_001039960.1 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr12:51853841 G>T maps to NM_001039960.1 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr12:100955673 G>T maps to ENST00000392986 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr12:100955673 G>T maps to ENST00000392986 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr12:109849745 G>C maps to NM_001101421.3 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr12:109849745 G>C maps to NM_001101421.3 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr12:113872018 C>A maps to NM_138432.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr12:113872018 C>A maps to NM_138432.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr12:123482023 C>T maps to NM_020845.2 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr12:123482023 C>T maps to NM_020845.2 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr12:133266863 A>T maps to NM_018663.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr12:133266863 A>T maps to NM_018663.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr13:102375270 G>C maps to NM_175929.2 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr13:102375270 G>C maps to NM_175929.2 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr14:21957420 T>C maps to NM_014828.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr14:21957420 T>C maps to NM_014828.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr14:64936394 G>C maps to NM_004857.3 *428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr14:64936394 G>C maps to NM_004857.3 *428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr15:43927556 C>G did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr15:43927556 C>G did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr16:23700834 C>T maps to NM_005030.3 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr16:23700834 C>T maps to NM_005030.3 F482F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr16:76496002 G>A did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr16:76496002 G>A did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr17:18155349 C>A maps to NM_002018.2 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr17:18155349 C>A maps to NM_002018.2 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr17:34192400 C>A did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr17:34192400 C>A did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr18:14106334 C>A maps to NM_145287.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr18:14106334 C>A maps to NM_145287.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr19:30193699 C>T maps to NM_001031726.2 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr19:30193699 C>T maps to NM_001031726.2 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr19:38860882 C>A maps to NM_021185.4 A1066A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr19:38860882 C>A maps to NM_021185.4 A1066A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr19:47503646 G>A maps to NM_004491.4 W1401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr19:47503646 G>A maps to NM_004491.4 W1401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr19:59073762 G>A maps to NM_198055.1 C627C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr19:59073762 G>A maps to NM_198055.1 C627C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr2:26682978 A>G maps to NM_194248.2 L1970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr2:26682978 A>G maps to NM_194248.2 L1970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr2:133543009 C>A maps to NM_207363.2 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr2:133543009 C>A maps to NM_207363.2 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr2:159530274 T>G did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr2:159530274 T>G did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr2:179428333 G>T maps to NM_133378.4 R24941R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr2:179428333 G>T maps to NM_133378.4 R24941R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr21:15599566 G>T maps to NM_144770.3 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr21:15599566 G>T maps to NM_144770.3 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr21:15599598 G>A maps to NM_144770.3 K277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr21:15599598 G>A maps to NM_144770.3 K277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr22:50279256 C>T maps to NM_014838.2 Y649Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr22:50279256 C>T maps to NM_014838.2 Y649Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr22:51137136 C>T maps to NM_001080420.1 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr22:51137136 C>T maps to NM_001080420.1 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr3:35732492 A>T maps to ENST00000458225 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr3:35732492 A>T maps to ENST00000458225 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr3:39306962 C>G maps to NM_001171174.1 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr3:39306962 C>G maps to NM_001171174.1 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr3:108211973 C>A maps to NM_014981.1 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr3:108211973 C>A maps to NM_014981.1 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr3:121643790 G>T did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr3:121643790 G>T did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr4:3134445 A>T maps to NM_002111.6 T798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr4:3134445 A>T maps to NM_002111.6 T798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr4:3768966 C>T maps to NM_000683.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr4:3768966 C>T maps to NM_000683.3 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr4:44177040 T>A maps to NM_198353.2 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr4:44177040 T>A maps to NM_198353.2 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr5:5486870 A>T maps to NM_015325.1 P2186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr5:5486870 A>T maps to NM_015325.1 P2186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr5:13708444 C>T did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr5:13708444 C>T did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr5:140222762 C>A maps to NM_018911.2 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr5:140222762 C>A maps to NM_018911.2 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr5:176794767 G>T maps to ENST00000398128 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr5:176794767 G>T maps to ENST00000398128 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr7:87785301 G>T maps to NM_021723.3 G630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr7:87785301 G>T maps to NM_021723.3 G630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr7:148767796 C>A maps to NM_152411.3 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr7:148767796 C>A maps to NM_152411.3 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr8:141521630 C>A maps to NM_017444.4 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr8:141521630 C>A maps to NM_017444.4 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr8:145738092 C>T maps to ENST00000428558 A939A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr8:145738092 C>T maps to ENST00000428558 A939A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr9:122011376 C>T maps to NM_014618.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr9:122011376 C>T maps to NM_014618.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chrX:1538001 C>T maps to NM_004192.3 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chrX:1538001 C>T maps to NM_004192.3 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chrX:37027193 G>A maps to NM_001013736.2 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chrX:37027193 G>A maps to NM_001013736.2 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chrX:44703890 G>C maps to NM_022076.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chrX:44703890 G>C maps to NM_022076.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chrX:73962795 G>C maps to NM_001008537.2 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chrX:73962795 G>C maps to NM_001008537.2 T532T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:40929122 C>G maps to NM_023070.2 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:40929122 C>G maps to NM_023070.2 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:44365305 T>A maps to NM_174963.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:44365305 T>A maps to NM_174963.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:86961315 C>T maps to NM_001285.3 Q691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:86961315 C>T maps to NM_001285.3 Q691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:151640991 C>T maps to ENST00000458013 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:151640991 C>T maps to ENST00000458013 Q344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:152276849 C>T maps to NM_002016.1 S3504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:152276849 C>T maps to NM_002016.1 S3504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:156106746 G>A maps to NM_170707.2 Q472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:156106746 G>A maps to NM_170707.2 Q472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:207751468 C>A maps to NM_000651.4 G1619G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:207751468 C>A maps to NM_000651.4 G1619G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:214542899 C>T maps to NM_005401.4 K1057K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:214542899 C>T maps to NM_005401.4 K1057K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:226125197 C>A maps to NM_003240.3 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:226125197 C>A maps to NM_003240.3 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:227170662 C>T maps to NM_020247.4 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:227170662 C>T maps to NM_020247.4 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:248458697 C>T maps to NM_001004692.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr1:248458697 C>T maps to NM_001004692.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr10:863816 G>A maps to NM_015155.1 Q515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr10:863816 G>A maps to NM_015155.1 Q515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr10:13240696 G>T maps to NM_182751.2 E711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr10:13240696 G>T maps to NM_182751.2 E711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr10:72020460 G>A maps to ENST00000277942 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr10:72020460 G>A maps to ENST00000277942 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr10:90521212 T>C maps to NM_001102469.1 N17N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr10:90521212 T>C maps to NM_001102469.1 N17N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr11:64883455 G>A maps to NM_003273.2 Q396Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr11:64883455 G>A maps to NM_003273.2 Q396Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr12:55759092 C>T maps to NM_001005497.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr12:55759092 C>T maps to NM_001005497.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr12:57594937 T>C did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr12:57594937 T>C did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr12:89917405 A>T maps to NM_003774.4 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr12:89917405 A>T maps to NM_003774.4 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr12:112665942 C>T maps to NM_001109662.2 G2096G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr12:112665942 C>T maps to NM_001109662.2 G2096G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr13:26975691 G>A maps to NM_001260.1 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr13:26975691 G>A maps to NM_001260.1 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr13:88327891 C>T maps to NM_015567.1 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr13:88327891 C>T maps to NM_015567.1 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr13:113777198 C>T maps to NM_000504.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr13:113777198 C>T maps to NM_000504.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr14:50616838 T>A maps to NM_006939.2 P757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr14:50616838 T>A maps to NM_006939.2 P757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr14:74874372 C>T maps to NM_001105579.1 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr14:74874372 C>T maps to NM_001105579.1 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr14:91787564 G>A maps to NM_001080414.2 Q476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr14:91787564 G>A maps to NM_001080414.2 Q476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr14:94722875 G>T maps to NM_058237.1 E649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr14:94722875 G>T maps to NM_058237.1 E649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr14:100125953 C>T maps to NM_001127258.1 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr14:100125953 C>T maps to NM_001127258.1 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr15:50264848 G>T maps to NM_024837.2 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr15:50264848 G>T maps to NM_024837.2 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr15:50769167 G>A maps to NM_005154.3 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr15:50769167 G>A maps to NM_005154.3 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr15:83820107 G>A maps to NM_016073.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr15:83820107 G>A maps to NM_016073.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr16:2201694 G>T did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr16:2201694 G>T did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr16:11004075 G>T maps to NM_000246.3 E950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr16:11004075 G>T maps to NM_000246.3 E950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr16:15797862 G>A maps to NM_001040114.1 T1975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr16:15797862 G>A maps to NM_001040114.1 T1975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr17:7576927 T>C did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr17:7576927 T>C did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr17:35306511 G>A maps to NM_012138.3 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr17:35306511 G>A maps to NM_012138.3 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr17:73624384 G>A maps to NM_004259.5 S906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr17:73624384 G>A maps to NM_004259.5 S906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr19:15052713 C>A maps to NM_012377.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr19:15052713 C>A maps to NM_012377.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr19:20736632 C>T maps to NM_001159293.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr19:20736632 C>T maps to NM_001159293.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr19:50713684 C>T maps to NM_001145809.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr19:50713684 C>T maps to NM_001145809.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr19:54401791 G>C maps to NM_002739.3 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr19:54401791 G>C maps to NM_002739.3 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:26203808 G>C maps to NM_002254.6 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:26203808 G>C maps to NM_002254.6 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:44099197 C>T maps to NM_022437.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:44099197 C>T maps to NM_022437.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:44162017 C>A did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:44162017 C>A did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:56149557 G>A maps to NM_001039349.1 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:56149557 G>A maps to NM_001039349.1 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:160663607 G>C maps to NM_001198759.1 V1622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:160663607 G>C maps to NM_001198759.1 V1622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:182387034 C>T maps to NM_000885.4 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:182387034 C>T maps to NM_000885.4 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:238483688 C>T maps to NM_022449.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:238483688 C>T maps to NM_022449.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:242380774 C>G maps to NM_014808.2 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr2:242380774 C>G maps to NM_014808.2 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr20:3739185 G>C maps to NM_001039140.1 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr20:3739185 G>C maps to NM_001039140.1 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr20:25197284 C>A maps to NM_001247.2 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr20:25197284 C>A maps to NM_001247.2 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr20:57769025 G>T maps to NM_178457.1 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr20:57769025 G>T maps to NM_178457.1 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr21:37741536 C>G maps to ENST00000290384 S625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr21:37741536 C>G maps to ENST00000290384 S625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr22:22868742 C>T maps to NM_080740.3 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr22:22868742 C>T maps to NM_080740.3 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr22:42606031 G>A maps to NM_005650.1 S1760S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr22:42606031 G>A maps to NM_005650.1 S1760S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr3:5246815 G>A maps to NM_014674.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr3:5246815 G>A maps to NM_014674.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr3:49278822 G>T did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr3:49278822 G>T did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr4:71702028 C>T maps to NM_002092.3 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr4:71702028 C>T maps to NM_002092.3 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr4:184366789 G>A maps to NM_017632.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr4:184366789 G>A maps to NM_017632.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr5:10256235 G>A maps to NM_012073.3 Q167Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr5:10256235 G>A maps to NM_012073.3 Q167Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr5:79770504 G>A maps to NM_014733.3 Q1439Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr5:79770504 G>A maps to NM_014733.3 Q1439Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr5:88018741 T>C maps to NM_002397.4 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr5:88018741 T>C maps to NM_002397.4 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr5:112175990 C>G maps to NM_001127510.2 S1567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr5:112175990 C>G maps to NM_001127510.2 S1567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr5:140580819 C>A maps to NM_018931.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr5:140580819 C>A maps to NM_018931.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr5:140763370 C>A maps to NM_018920.2 S302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr5:140763370 C>A maps to NM_018920.2 S302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr6:30530164 G>T did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr6:30530164 G>T did not map to a codon.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr6:134210615 G>A maps to NM_003206.3 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr6:134210615 G>A maps to NM_003206.3 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr7:4917455 C>T maps to NM_018059.4 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr7:4917455 C>T maps to NM_018059.4 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr7:82584859 A>G maps to NM_033026.5 S1803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr7:82584859 A>G maps to NM_033026.5 S1803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr7:99711344 G>A maps to ENST00000472509 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr7:99711344 G>A maps to ENST00000472509 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr7:100677498 G>A maps to NM_001040105.1 T934T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr7:100677498 G>A maps to NM_001040105.1 T934T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr7:133689721 G>T maps to NM_021807.3 V802V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr7:133689721 G>T maps to NM_021807.3 V802V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CV-6948-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr7:154862902 G>A maps to NM_024012.2 L98L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CV-6948-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr7:154862902 G>A maps to NM_024012.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr8:8234393 C>A maps to NM_001080826.1 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr8:8234393 C>A maps to NM_001080826.1 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr8:56270345 G>T maps to NM_052898.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr8:56270345 G>T maps to NM_052898.1 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr8:87076790 G>T maps to ENST00000276616 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr8:87076790 G>T maps to ENST00000276616 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr8:131073298 T>C maps to NM_018482.2 T906T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr8:131073298 T>C maps to NM_018482.2 T906T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr9:105767307 C>G maps to NM_001340.3 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chr9:105767307 C>G maps to NM_001340.3 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chrX:26212040 G>C maps to NM_173523.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chrX:26212040 G>C maps to NM_173523.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chrX:51639729 C>T maps to NM_001005333.1 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6948-01A-11D-1912-08 chrX:51639729 C>T maps to NM_001005333.1 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr11:755975 G>A maps to NM_006755.1 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr11:755975 G>A maps to NM_006755.1 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr12:8212706 G>A maps to NM_004054.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr12:8212706 G>A maps to NM_004054.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr14:23447603 G>A maps to NM_032876.4 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr14:23447603 G>A maps to NM_032876.4 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr14:24679886 A>G maps to NM_014169.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr14:24679886 A>G maps to NM_014169.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr14:89091393 C>T maps to ENST00000380664 A1606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr14:89091393 C>T maps to ENST00000380664 A1606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr18:67801777 C>T did not map to a codon.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr18:67801777 C>T did not map to a codon.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr19:42584698 C>T maps to ENST00000222339 S737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr19:42584698 C>T maps to ENST00000222339 S737S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr20:33519178 G>A maps to NM_000178.2 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr20:33519178 G>A maps to NM_000178.2 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr22:26164179 T>C maps to ENST00000407587 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr22:26164179 T>C maps to ENST00000407587 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr3:122354784 C>T maps to NM_001113523.1 F625F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr3:122354784 C>T maps to NM_001113523.1 F625F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr3:151112628 C>T maps to NM_053002.4 Q1897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr3:151112628 C>T maps to NM_053002.4 Q1897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr3:185975670 C>T maps to NM_001346.2 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr3:185975670 C>T maps to NM_001346.2 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr4:49030674 C>A maps to NM_025087.2 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr4:49030674 C>A maps to NM_025087.2 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr6:51524465 C>T maps to NM_138694.3 L3486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr6:51524465 C>T maps to NM_138694.3 L3486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr6:71247997 C>T maps to NM_001162529.1 L1374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr6:71247997 C>T maps to NM_001162529.1 L1374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr7:91659266 G>T maps to NM_005751.4 G1403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr7:91659266 G>T maps to NM_005751.4 G1403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr8:52336258 G>A maps to NM_144651.4 F557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr8:52336258 G>A maps to NM_144651.4 F557F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr8:103287968 T>A maps to NM_015902.4 V2199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr8:103287968 T>A maps to NM_015902.4 V2199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr9:3263050 G>A maps to NM_134428.1 R497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chr9:3263050 G>A maps to NM_134428.1 R497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chrX:3241943 C>T maps to NM_015419.3 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chrX:3241943 C>T maps to NM_015419.3 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chrX:108718933 A>G maps to ENST00000218006 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chrX:108718933 A>G maps to ENST00000218006 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chrX:138832232 C>A maps to NM_173694.4 E930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6950-01A-11D-1912-08 chrX:138832232 C>A maps to NM_173694.4 E930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr1:33116073 C>T maps to NM_178547.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr1:33116073 C>T maps to NM_178547.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr1:35452857 T>C maps to NM_007167.3 L1275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr1:35452857 T>C maps to NM_007167.3 L1275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr1:55145694 C>T maps to ENST00000454855 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr1:55145694 C>T maps to ENST00000454855 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr1:67516167 G>A maps to NM_015139.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr1:67516167 G>A maps to NM_015139.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr1:158595953 G>T maps to NM_003126.2 L1964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr1:158595953 G>T maps to NM_003126.2 L1964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr1:248637568 G>A maps to NM_001005495.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr1:248637568 G>A maps to NM_001005495.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr10:43088342 T>C maps to NM_006955.1 R685R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr10:43088342 T>C maps to NM_006955.1 R685R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr10:119799784 A>G maps to ENST00000369199 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr10:119799784 A>G maps to ENST00000369199 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr10:124348655 C>T maps to ENST00000368915 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr10:124348655 C>T maps to ENST00000368915 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr11:1263374 C>T maps to ENST00000447027 T1758T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr11:1263374 C>T maps to ENST00000447027 T1758T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr11:68318641 G>T maps to NM_001164160.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr11:68318641 G>T maps to NM_001164160.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr11:72945506 C>T maps to NM_176071.1 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr11:72945506 C>T maps to NM_176071.1 F101F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr12:49488007 G>A maps to NM_021044.2 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr12:49488007 G>A maps to NM_021044.2 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr12:102030482 C>T maps to NM_002465.2 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr12:102030482 C>T maps to NM_002465.2 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr12:123019278 A>G maps to NM_014708.4 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr12:123019278 A>G maps to NM_014708.4 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr13:114009695 G>C maps to NM_024719.2 Y94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr13:114009695 G>C maps to NM_024719.2 Y94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr15:42166141 G>T maps to ENST00000320955 I1597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr15:42166141 G>T maps to ENST00000320955 I1597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr15:78640276 C>T maps to NM_004378.2 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr15:78640276 C>T maps to NM_004378.2 G124G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CV-6951-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr17:15902869 C>G maps to NM_017775.2 S24*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CV-6951-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr17:15902869 C>G maps to NM_017775.2 S24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr17:77073808 C>G maps to NM_001042573.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr17:77073808 C>G maps to NM_001042573.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr19:48917262 C>T maps to NM_000836.2 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr19:48917262 C>T maps to NM_000836.2 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr19:56114116 C>T maps to NM_153219.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr19:56114116 C>T maps to NM_153219.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr19:58118330 C>T maps to NM_020880.3 R480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr19:58118330 C>T maps to NM_020880.3 R480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr2:27804295 G>A maps to NM_032266.3 E1619E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr2:27804295 G>A maps to NM_032266.3 E1619E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr2:27804509 G>T maps to NM_032266.3 E1691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr2:27804509 G>T maps to NM_032266.3 E1691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr2:68365915 G>C maps to NM_138458.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr2:68365915 G>C maps to NM_138458.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr2:128712890 C>A maps to NM_001145928.1 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr2:128712890 C>A maps to NM_001145928.1 V723V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr2:189434753 G>T did not map to a codon.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr2:189434753 G>T did not map to a codon.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr20:3726198 G>A maps to NM_052970.4 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr20:3726198 G>A maps to NM_052970.4 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr20:32217676 C>T maps to NM_005093.3 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr20:32217676 C>T maps to NM_005093.3 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr3:138023769 G>A maps to ENST00000333911 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr3:138023769 G>A maps to ENST00000333911 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr4:164394487 T>A maps to NM_032136.4 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr4:164394487 T>A maps to NM_032136.4 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr6:3045940 C>T maps to NM_001012983.1 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr6:3045940 C>T maps to NM_001012983.1 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr6:28268866 C>G maps to NM_032507.3 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr6:28268866 C>G maps to NM_032507.3 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr6:37344796 A>G maps to NM_003958.3 E408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr6:37344796 A>G maps to NM_003958.3 E408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr7:15725703 G>T maps to NM_005924.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr7:15725703 G>T maps to NM_005924.4 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr7:57188596 A>G maps to NM_033273.1 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr7:57188596 A>G maps to NM_033273.1 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr7:92761450 C>T maps to NM_152703.2 L1278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr7:92761450 C>T maps to NM_152703.2 L1278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr7:117450884 G>A maps to NM_033427.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr7:117450884 G>A maps to NM_033427.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr8:133898694 G>T maps to NM_003235.4 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr8:133898694 G>T maps to NM_003235.4 E360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr9:33034295 G>T maps to NM_001539.2 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr9:33034295 G>T maps to NM_001539.2 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr9:98239881 C>A maps to NM_000264.3 G484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr9:98239881 C>A maps to NM_000264.3 G484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr9:111903701 C>T maps to NM_014334.2 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6951-01A-11D-1912-08 chr9:111903701 C>T maps to NM_014334.2 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr1:60309234 A>G maps to NM_015888.4 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr1:60309234 A>G maps to NM_015888.4 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr1:108116683 T>A maps to NM_006113.4 G829G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr1:108116683 T>A maps to NM_006113.4 G829G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr1:114499829 C>T maps to ENST00000426820 F630F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr1:114499829 C>T maps to ENST00000426820 F630F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr1:117158882 G>A maps to NM_001542.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr1:117158882 G>A maps to NM_001542.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr1:152188023 C>T maps to NM_001009931.1 S2027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr1:152188023 C>T maps to NM_001009931.1 S2027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr1:159558170 G>C maps to NM_001639.3 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr1:159558170 G>C maps to NM_001639.3 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr10:59976031 G>A maps to NM_152230.4 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr10:59976031 G>A maps to NM_152230.4 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr11:5173295 G>A maps to NM_012375.2 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr11:5173295 G>A maps to NM_012375.2 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr11:62285787 T>C maps to NM_001620.1 G5367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr11:62285787 T>C maps to NM_001620.1 G5367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr11:72013355 G>A maps to NM_030813.3 R417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr11:72013355 G>A maps to NM_030813.3 R417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr11:118375348 C>A maps to NM_001197104.1 V2914V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr11:118375348 C>A maps to NM_001197104.1 V2914V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr11:120998602 C>T maps to NM_005422.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr11:120998602 C>T maps to NM_005422.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr12:53823689 C>T maps to NM_020547.2 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr12:53823689 C>T maps to NM_020547.2 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr12:93100818 C>T maps to NM_001037671.3 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr12:93100818 C>T maps to NM_001037671.3 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr15:79058841 G>A maps to ENST00000258883 A1137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr15:79058841 G>A maps to ENST00000258883 A1137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr15:100269525 G>A maps to NM_152449.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr15:100269525 G>A maps to NM_152449.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr16:75513141 T>C maps to NM_021615.4 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr16:75513141 T>C maps to NM_021615.4 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr16:84104309 T>C maps to NM_003791.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr16:84104309 T>C maps to NM_003791.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr17:42992692 C>T maps to NM_002055.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr17:42992692 C>T maps to NM_002055.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr17:46862374 G>A maps to NM_001130918.1 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr17:46862374 G>A maps to NM_001130918.1 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr18:29055985 C>T maps to NM_001944.2 S921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr18:29055985 C>T maps to NM_001944.2 S921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr18:70461477 C>T maps to NM_153181.2 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr18:70461477 C>T maps to NM_153181.2 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr19:44536635 C>A maps to NM_001129996.1 S310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr19:44536635 C>A maps to NM_001129996.1 S310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr19:52619979 G>T maps to NM_178523.3 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr19:52619979 G>T maps to NM_178523.3 S146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr2:128044294 T>C maps to NM_000122.1 E442E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr2:128044294 T>C maps to NM_000122.1 E442E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr2:141081530 C>A maps to NM_018557.2 E4149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr2:141081530 C>A maps to NM_018557.2 E4149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr2:145156647 A>G maps to NM_014795.3 N702N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr2:145156647 A>G maps to NM_014795.3 N702N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr2:149526742 G>A maps to NM_015630.3 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr2:149526742 G>A maps to NM_015630.3 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr2:197738420 C>G maps to NM_024989.3 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr2:197738420 C>G maps to NM_024989.3 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr2:198285203 C>T maps to NM_012433.2 K121K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr2:198285203 C>T maps to NM_012433.2 K121K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr2:231944261 A>G maps to NM_002807.3 E391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr2:231944261 A>G maps to NM_002807.3 E391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr22:24432586 A>G maps to NM_012295.3 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr22:24432586 A>G maps to NM_012295.3 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr22:46658433 G>A maps to NM_006071.1 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr22:46658433 G>A maps to NM_006071.1 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr3:111688670 C>T maps to NM_001134438.1 L1150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr3:111688670 C>T maps to NM_001134438.1 L1150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr3:141499574 G>T maps to NM_139209.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr3:141499574 G>T maps to NM_139209.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr3:164735777 A>T maps to NM_001041.3 L1167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr3:164735777 A>T maps to NM_001041.3 L1167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr3:170150426 C>T maps to NM_005602.5 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr3:170150426 C>T maps to NM_005602.5 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr4:86786 A>G maps to NM_182524.2 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr4:86786 A>G maps to NM_182524.2 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr4:48496197 C>T maps to NM_175619.1 C404C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr4:48496197 C>T maps to NM_175619.1 C404C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr4:187525002 G>C maps to ENST00000260147 Y3562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr4:187525002 G>C maps to ENST00000260147 Y3562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr5:101834542 G>A maps to NM_173488.3 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr5:101834542 G>A maps to NM_173488.3 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr5:130764619 C>G maps to ENST00000514667 V1635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr5:130764619 C>G maps to ENST00000514667 V1635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr5:132222031 C>T maps to NM_014423.3 K1023K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr5:132222031 C>T maps to NM_014423.3 K1023K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr6:11104999 G>A maps to NM_207582.2 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr6:11104999 G>A maps to NM_207582.2 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr6:43096754 C>T maps to NM_002821.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr6:43096754 C>T maps to NM_002821.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr6:89650811 G>C maps to NM_003800.3 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr6:89650811 G>C maps to NM_003800.3 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr6:117710591 G>A maps to NM_002944.2 R560R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr6:117710591 G>A maps to NM_002944.2 R560R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr6:139363992 C>T maps to NM_021243.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr6:139363992 C>T maps to NM_021243.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr7:39606029 C>T maps to NM_020192.3 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr7:39606029 C>T maps to NM_020192.3 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr7:123185710 A>C maps to NM_005000.2 L68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr7:123185710 A>C maps to NM_005000.2 L68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr8:1497608 G>A maps to ENST00000357934 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr8:1497608 G>A maps to ENST00000357934 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr8:17142025 A>T maps to NM_152415.2 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr8:17142025 A>T maps to NM_152415.2 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr8:23709898 T>A did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr8:23709898 T>A did not map to a codon.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr8:100831672 C>T maps to NM_017890.3 P2910P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr8:100831672 C>T maps to NM_017890.3 P2910P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CV-6952-01A-11D-1912-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-CV-6952-01A-11D-1912-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr8:121475946 T>C maps to NM_022045.3 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr8:121475946 T>C maps to NM_022045.3 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr8:127569306 C>A maps to NM_174911.4 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr8:127569306 C>A maps to NM_174911.4 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr8:144993791 C>T maps to NM_201380.2 V3536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr8:144993791 C>T maps to NM_201380.2 V3536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr9:19516219 G>C maps to NM_020344.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr9:19516219 G>C maps to NM_020344.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr9:131285594 A>G maps to NM_001003722.1 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chr9:131285594 A>G maps to NM_001003722.1 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chrX:47002065 G>A maps to NM_019056.5 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chrX:47002065 G>A maps to NM_019056.5 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chrX:65393632 C>T maps to NM_138737.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chrX:65393632 C>T maps to NM_138737.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chrX:130415219 T>G maps to NM_001170961.1 R540R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chrX:130415219 T>G maps to NM_001170961.1 R540R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chrX:138686865 T>A maps to ENST00000370578 R718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6952-01A-11D-1912-08 chrX:138686865 T>A maps to ENST00000370578 R718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr1:32280967 C>T did not map to a codon.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr1:32280967 C>T did not map to a codon.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr1:37271717 G>A maps to NM_000831.3 I767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr1:37271717 G>A maps to NM_000831.3 I767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr1:154295467 G>A maps to NM_080429.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr1:154295467 G>A maps to NM_080429.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr1:192335208 T>C maps to NM_001039152.3 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr1:192335208 T>C maps to NM_001039152.3 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr1:213414330 A>C maps to NM_012424.3 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr1:213414330 A>C maps to NM_012424.3 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr10:61005099 G>T maps to NM_032439.3 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr10:61005099 G>T maps to NM_032439.3 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr11:55587491 C>T maps to ENST00000395203 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr11:55587491 C>T maps to ENST00000395203 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr12:10167882 C>T maps to NM_001129998.1 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr12:10167882 C>T maps to NM_001129998.1 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr13:52542594 G>A maps to NM_000053.2 G564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr13:52542594 G>A maps to NM_000053.2 G564G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr13:72053409 T>C maps to ENST00000359684 Q641Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr13:72053409 T>C maps to ENST00000359684 Q641Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr14:30135409 G>A maps to NM_002742.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr14:30135409 G>A maps to NM_002742.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr14:68215204 C>T maps to NM_015346.3 W2523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr14:68215204 C>T maps to NM_015346.3 W2523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr14:92601739 C>T maps to NM_017437.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr14:92601739 C>T maps to NM_017437.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr14:103573993 C>T maps to NM_001077594.1 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr14:103573993 C>T maps to NM_001077594.1 F576F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr15:49127201 G>A maps to NM_203349.3 Q501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr15:49127201 G>A maps to NM_203349.3 Q501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr16:2347778 G>A maps to NM_001089.2 I680I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr16:2347778 G>A maps to NM_001089.2 I680I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr17:39580481 G>A maps to NM_003770.4 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr17:39580481 G>A maps to NM_003770.4 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr19:22156896 G>T maps to NM_007153.3 Y313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr19:22156896 G>T maps to NM_007153.3 Y313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr19:50102548 G>A maps to NM_020719.1 K1233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr19:50102548 G>A maps to NM_020719.1 K1233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr2:3726068 G>A maps to ENST00000403787 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr2:3726068 G>A maps to ENST00000403787 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr2:202150038 C>T maps to NM_001080125.1 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr2:202150038 C>T maps to NM_001080125.1 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr2:220419304 C>T maps to NM_015311.2 S1589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr2:220419304 C>T maps to NM_015311.2 S1589S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr22:37098537 C>A maps to NM_006078.3 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr22:37098537 C>A maps to NM_006078.3 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr3:113377776 G>A maps to NM_001009899.2 Q918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr3:113377776 G>A maps to NM_001009899.2 Q918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr3:183858376 C>A maps to NM_003907.2 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr3:183858376 C>A maps to NM_003907.2 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr5:132556520 G>A maps to NM_015082.1 D459D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr5:132556520 G>A maps to NM_015082.1 D459D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr5:140779286 C>T maps to NM_018925.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr5:140779286 C>T maps to NM_018925.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr6:20124637 C>T did not map to a codon.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr6:20124637 C>T did not map to a codon.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr6:36449468 G>C maps to NM_173562.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr6:36449468 G>C maps to NM_173562.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr6:118228942 G>A maps to NM_001029858.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr6:118228942 G>A maps to NM_001029858.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr7:141333765 C>T maps to NM_018238.3 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr7:141333765 C>T maps to NM_018238.3 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr8:41791630 G>A maps to NM_006766.3 T1369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr8:41791630 G>A maps to NM_006766.3 T1369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr9:19346743 C>G maps to NM_017925.4 S1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr9:19346743 C>G maps to NM_017925.4 S1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chrX:70342192 G>A maps to ENST00000333646 Q415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chrX:70342192 G>A maps to ENST00000333646 Q415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr1:15959964 G>A maps to NM_032341.4 Q179Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr1:15959964 G>A maps to NM_032341.4 Q179Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr1:108307727 C>T maps to NM_006113.4 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr1:108307727 C>T maps to NM_006113.4 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr1:168274252 C>A maps to NM_005149.2 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr1:168274252 C>A maps to NM_005149.2 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr1:247769354 C>T maps to NM_001001914.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr1:247769354 C>T maps to NM_001001914.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr11:5344900 A>G maps to NM_033180.4 C209C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr11:5344900 A>G maps to NM_033180.4 C209C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr11:55927528 G>A maps to NM_001004058.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr11:55927528 G>A maps to NM_001004058.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr11:76371158 A>T maps to NM_001128922.1 L493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr11:76371158 A>T maps to NM_001128922.1 L493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr11:118377361 G>T did not map to a codon.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr11:118377361 G>T did not map to a codon.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr12:9313712 C>T did not map to a codon.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr12:9313712 C>T did not map to a codon.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr12:95887870 A>G maps to NM_006838.3 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr12:95887870 A>G maps to NM_006838.3 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr12:101732714 A>G maps to NM_014503.2 K1331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr12:101732714 A>G maps to NM_014503.2 K1331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr12:122213540 C>T maps to NM_001080825.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr12:122213540 C>T maps to NM_001080825.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr14:30046530 C>A maps to NM_002742.2 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr14:30046530 C>A maps to NM_002742.2 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr14:75369020 C>G maps to NM_001933.4 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr14:75369020 C>G maps to NM_001933.4 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr15:40756082 A>G maps to NM_014952.3 R613R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr15:40756082 A>G maps to NM_014952.3 R613R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr15:53998226 T>C maps to NM_182758.2 K333K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr15:53998226 T>C maps to NM_182758.2 K333K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr16:50733834 C>T maps to NM_022162.1 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr16:50733834 C>T maps to NM_022162.1 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr16:67778257 G>A maps to NM_020850.1 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr16:67778257 G>A maps to NM_020850.1 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr16:72094608 A>G maps to NM_005143.3 Q347Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr16:72094608 A>G maps to NM_005143.3 Q347Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr17:36868951 G>A maps to NM_005937.3 K243K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr17:36868951 G>A maps to NM_005937.3 K243K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr19:42471440 G>A maps to ENST00000441343 Y991Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr19:42471440 G>A maps to ENST00000441343 Y991Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr2:31600013 T>A maps to NM_000379.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr2:31600013 T>A maps to NM_000379.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr2:31805846 G>A maps to NM_000348.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr2:31805846 G>A maps to NM_000348.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr2:176964534 T>C maps to NM_021193.3 C2C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr2:176964534 T>C maps to NM_021193.3 C2C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr2:233128056 C>T maps to NM_152383.4 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr2:233128056 C>T maps to NM_152383.4 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr2:236877175 G>C maps to NM_001037131.1 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr2:236877175 G>C maps to NM_001037131.1 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr20:3766500 C>A maps to NM_001810.5 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr20:3766500 C>A maps to NM_001810.5 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr20:32026758 G>A maps to NM_003098.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr20:32026758 G>A maps to NM_003098.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr20:44416544 T>C maps to NM_080614.1 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr20:44416544 T>C maps to NM_080614.1 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr20:50140071 C>T maps to NM_012340.3 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr20:50140071 C>T maps to NM_012340.3 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr20:50705114 G>A maps to NM_199427.2 H348H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr20:50705114 G>A maps to NM_199427.2 H348H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr22:20229736 G>A maps to ENST00000425986 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr22:20229736 G>A maps to ENST00000425986 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr3:30732962 G>T maps to NM_001024847.2 E551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr3:30732962 G>T maps to NM_001024847.2 E551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr3:141328365 G>T did not map to a codon.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr3:141328365 G>T did not map to a codon.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr4:38800206 C>T maps to NM_003263.3 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr4:38800206 C>T maps to NM_003263.3 Q82Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr4:48380074 C>G maps to NM_020846.1 S234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr4:48380074 C>G maps to NM_020846.1 S234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr4:66213888 T>A maps to NM_004439.5 P847P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr4:66213888 T>A maps to NM_004439.5 P847P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr5:13762884 C>T maps to NM_001369.2 W3409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr5:13762884 C>T maps to NM_001369.2 W3409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr5:62073028 G>C did not map to a codon.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr5:62073028 G>C did not map to a codon.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr5:90040950 T>A maps to NM_032119.3 P3546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr5:90040950 T>A maps to NM_032119.3 P3546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr5:140553867 C>T maps to NM_018940.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr5:140553867 C>T maps to NM_018940.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr5:180483001 T>G maps to NM_152547.4 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr5:180483001 T>G maps to NM_152547.4 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr6:25826724 G>A maps to NM_005074.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr6:25826724 G>A maps to NM_005074.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr6:44272034 C>T maps to NM_020745.2 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr6:44272034 C>T maps to NM_020745.2 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr6:117086361 G>A maps to NM_001085480.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr6:117086361 G>A maps to NM_001085480.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr7:1037376 C>A maps to NM_032350.5 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr7:1037376 C>A maps to NM_032350.5 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr7:11630195 G>A maps to ENST00000423059 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr7:11630195 G>A maps to ENST00000423059 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr8:16948071 A>T maps to NM_181723.2 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr8:16948071 A>T maps to NM_181723.2 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr8:124219420 G>C maps to NM_032899.4 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr8:124219420 G>C maps to NM_032899.4 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr9:100895439 A>G maps to NM_052820.3 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr9:100895439 A>G maps to NM_052820.3 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr9:113704007 C>T maps to NM_057159.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr9:113704007 C>T maps to NM_057159.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chrX:128640092 G>A maps to NM_003069.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chrX:128640092 G>A maps to NM_003069.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr19:3011065 G>A maps to NM_003260.4 H322H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6954-01A-11D-1912-08 chr19:3011065 G>A maps to NM_003260.4 H322H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr1:6534541 G>A maps to NM_198681.2 Y213Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr1:6534541 G>A maps to NM_198681.2 Y213Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr1:53930413 G>A maps to NM_033067.1 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr1:53930413 G>A maps to NM_033067.1 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr1:57257876 G>T maps to NM_001004303.4 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr1:57257876 G>T maps to NM_001004303.4 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr1:248224879 C>A maps to NM_001004687.1 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr1:248224879 C>A maps to NM_001004687.1 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr1:248366773 C>G maps to NM_001004689.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr1:248366773 C>G maps to NM_001004689.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr10:12197793 G>A maps to NM_018144.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr10:12197793 G>A maps to NM_018144.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr10:91066450 A>T maps to NM_001547.4 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr10:91066450 A>T maps to NM_001547.4 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr10:123970683 G>A maps to NM_206862.2 S2248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr10:123970683 G>A maps to NM_206862.2 S2248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr11:3727720 G>C maps to NM_016320.4 S960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr11:3727720 G>C maps to NM_016320.4 S960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr11:18467777 G>A maps to NM_017448.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr11:18467777 G>A maps to NM_017448.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr12:29486609 C>T maps to NM_018099.3 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr12:29486609 C>T maps to NM_018099.3 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr12:53509200 C>T maps to NM_003578.3 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr12:53509200 C>T maps to NM_003578.3 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr12:56075774 C>T maps to NM_152637.2 C79C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr12:56075774 C>T maps to NM_152637.2 C79C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr12:120166408 G>C maps to ENST00000392521 L1163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr12:120166408 G>C maps to ENST00000392521 L1163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr14:44975152 A>T maps to NM_032135.3 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr14:44975152 A>T maps to NM_032135.3 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr14:94060061 G>A maps to ENST00000393153 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr14:94060061 G>A maps to ENST00000393153 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr14:105411953 G>A maps to NM_138420.2 V3278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr14:105411953 G>A maps to NM_138420.2 V3278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr15:39881287 G>A did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr15:39881287 G>A did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr16:57101665 C>T maps to NM_032206.3 L1475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr16:57101665 C>T maps to NM_032206.3 L1475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr17:1387007 G>A maps to NM_001080779.1 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr17:1387007 G>A maps to NM_001080779.1 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr17:26948138 G>A maps to NM_014680.2 I1703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr17:26948138 G>A maps to NM_014680.2 I1703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr17:76506501 G>A maps to ENST00000389840 I1396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr17:76506501 G>A maps to ENST00000389840 I1396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr17:79872319 G>A maps to NM_016538.2 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr17:79872319 G>A maps to NM_016538.2 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr2:74733101 C>T maps to NM_032673.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr2:74733101 C>T maps to NM_032673.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr2:141250262 C>G did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr2:141250262 C>G did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr2:232123815 G>A did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr2:232123815 G>A did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr21:19704464 C>G maps to NM_002772.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr21:19704464 C>G maps to NM_002772.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr22:43870808 C>T maps to NM_001044370.1 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr22:43870808 C>T maps to NM_001044370.1 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr3:88205751 G>A maps to NM_173824.3 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr3:88205751 G>A maps to NM_173824.3 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr4:24801553 G>C maps to NM_003102.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr4:24801553 G>C maps to NM_003102.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr4:187629099 G>A maps to ENST00000260147 R628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr4:187629099 G>A maps to ENST00000260147 R628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr5:140778899 A>T maps to NM_018925.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr5:140778899 A>T maps to NM_018925.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr5:140810886 C>T maps to NM_003735.2 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr5:140810886 C>T maps to NM_003735.2 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr5:160033922 C>T maps to NM_025153.2 L1003L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr5:160033922 C>T maps to NM_025153.2 L1003L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr6:1313526 C>G maps to NM_033260.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr6:1313526 C>G maps to NM_033260.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr7:81714096 G>A maps to NM_000722.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr7:81714096 G>A maps to NM_000722.2 R216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr7:98446223 C>T maps to NM_001134450.1 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr7:98446223 C>T maps to NM_001134450.1 Q367Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr7:121942916 G>A maps to NM_001024613.2 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr7:121942916 G>A maps to NM_001024613.2 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr8:11188845 C>T maps to NM_054028.1 C77C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr8:11188845 C>T maps to NM_054028.1 C77C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr8:77618161 C>T maps to NM_024721.4 I613I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr8:77618161 C>T maps to NM_024721.4 I613I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr8:95547109 T>G maps to NM_015496.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr8:95547109 T>G maps to NM_015496.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr8:125498990 C>T maps to NM_007218.3 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr8:125498990 C>T maps to NM_007218.3 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr9:35609463 C>A maps to NM_006285.2 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr9:35609463 C>A maps to NM_006285.2 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr9:136220668 G>A maps to NM_003172.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr9:136220668 G>A maps to NM_003172.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chrX:17819470 G>T maps to NM_021785.4 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chrX:17819470 G>T maps to NM_021785.4 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chrX:34961652 C>T maps to NM_152631.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chrX:34961652 C>T maps to NM_152631.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chrX:70787879 C>T maps to NM_181672.2 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chrX:70787879 C>T maps to NM_181672.2 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chrX:120007814 C>A maps to NM_001145718.1 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chrX:120007814 C>A maps to NM_001145718.1 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr1:57257987 G>T maps to NM_001004303.4 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr1:57257987 G>T maps to NM_001004303.4 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr1:97915725 G>C maps to NM_000110.3 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr1:97915725 G>C maps to NM_000110.3 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr1:151150568 C>T maps to ENST00000354473 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr1:151150568 C>T maps to ENST00000354473 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr1:155223907 A>T maps to ENST00000368370 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr1:155223907 A>T maps to ENST00000368370 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr1:211751729 G>A maps to NM_021194.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr1:211751729 G>A maps to NM_021194.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr1:227842403 A>G maps to NM_178549.3 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr1:227842403 A>G maps to NM_178549.3 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr10:15726023 C>A maps to NM_003638.1 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr10:15726023 C>A maps to NM_003638.1 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr10:27366290 C>T maps to NM_014915.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr10:27366290 C>T maps to NM_014915.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr10:43650761 G>A maps to NM_018590.3 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr10:43650761 G>A maps to NM_018590.3 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr11:18257395 C>T maps to NM_006512.3 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr11:18257395 C>T maps to NM_006512.3 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr11:75277798 C>T maps to NM_001235.2 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr11:75277798 C>T maps to NM_001235.2 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr11:121444947 A>T did not map to a codon.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr11:121444947 A>T did not map to a codon.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr12:49319148 C>A maps to NM_016594.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr12:49319148 C>A maps to NM_016594.2 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr12:58088660 G>A maps to NM_006812.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr12:58088660 G>A maps to NM_006812.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr12:109017612 C>T maps to ENST00000228463 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr12:109017612 C>T maps to ENST00000228463 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr12:121000764 G>T maps to ENST00000458409 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr12:121000764 G>T maps to ENST00000458409 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr12:121434486 T>A maps to NM_000545.5 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr12:121434486 T>A maps to NM_000545.5 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr13:88329859 C>A maps to NM_015567.1 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr13:88329859 C>A maps to NM_015567.1 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr13:95055461 G>T maps to NM_005708.3 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr13:95055461 G>T maps to NM_005708.3 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr13:111919972 T>C maps to NM_001113511.1 Y364Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr13:111919972 T>C maps to NM_001113511.1 Y364Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr14:20711093 C>T maps to NM_001004479.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr14:20711093 C>T maps to NM_001004479.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr14:21955827 G>A maps to NM_014828.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr14:21955827 G>A maps to NM_014828.2 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr14:61917603 C>T maps to NM_006255.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr14:61917603 C>T maps to NM_006255.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr14:78161200 C>T maps to NM_006020.2 W112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr14:78161200 C>T maps to NM_006020.2 W112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr14:103148295 A>G maps to NM_015156.2 Q139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr14:103148295 A>G maps to NM_015156.2 Q139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr15:23890015 C>T maps to NM_019066.4 W958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr15:23890015 C>T maps to NM_019066.4 W958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr15:75498856 T>C maps to NM_015492.4 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr15:75498856 T>C maps to NM_015492.4 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr16:20797458 T>G maps to NM_005622.3 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr16:20797458 T>G maps to NM_005622.3 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr17:7251468 C>G maps to NM_014716.3 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr17:7251468 C>G maps to NM_014716.3 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr17:18833956 C>T maps to NM_002767.2 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr17:18833956 C>T maps to NM_002767.2 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr17:66267355 G>A maps to NM_004694.4 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr17:66267355 G>A maps to NM_004694.4 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr18:13826438 C>A maps to NM_005913.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr18:13826438 C>A maps to NM_005913.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr18:22807173 C>T maps to NM_015461.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr18:22807173 C>T maps to NM_015461.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr19:4538050 C>T maps to NM_052972.2 Q315Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr19:4538050 C>T maps to NM_052972.2 Q315Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr19:19766740 C>G maps to NM_020410.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr19:19766740 C>G maps to NM_020410.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr19:38057173 C>T maps to NM_016536.3 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr19:38057173 C>T maps to NM_016536.3 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr19:43529017 G>A maps to ENST00000306308 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr19:43529017 G>A maps to ENST00000306308 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr19:57133863 G>T maps to NM_021216.4 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr19:57133863 G>T maps to NM_021216.4 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr2:26702479 G>T maps to NM_194248.2 R652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr2:26702479 G>T maps to NM_194248.2 R652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr2:74652826 G>C maps to NM_032118.2 *335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr2:74652826 G>C maps to NM_032118.2 *335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr2:166003415 G>A maps to NM_006922.3 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr2:166003415 G>A maps to NM_006922.3 R502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr2:189458683 A>T maps to NM_016315.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr2:189458683 A>T maps to NM_016315.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr2:241069333 C>T maps to NM_138336.1 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr2:241069333 C>T maps to NM_138336.1 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr2:242650883 C>T maps to NM_032329.4 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr2:242650883 C>T maps to NM_032329.4 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr20:3147716 C>T maps to NM_014731.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr20:3147716 C>T maps to NM_014731.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr20:23614553 T>A maps to NM_000099.2 *147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr20:23614553 T>A maps to NM_000099.2 *147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr21:11058237 G>A maps to NM_182482.2 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr21:11058237 G>A maps to NM_182482.2 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr22:46931726 G>T maps to NM_014246.1 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr22:46931726 G>T maps to NM_014246.1 I447I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr3:89456491 C>G maps to NM_005233.5 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr3:89456491 C>G maps to NM_005233.5 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr3:140281752 C>A maps to NM_022131.2 C771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr3:140281752 C>A maps to NM_022131.2 C771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr4:119649745 A>T maps to ENST00000379735 I977I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr4:119649745 A>T maps to ENST00000379735 I977I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr4:151168814 G>A maps to NM_001040261.4 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr4:151168814 G>A maps to NM_001040261.4 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr4:177077228 G>T did not map to a codon.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr4:177077228 G>T did not map to a codon.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr5:13928287 C>A did not map to a codon.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr5:13928287 C>A did not map to a codon.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr5:90106736 C>T maps to NM_032119.3 F5220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr5:90106736 C>T maps to NM_032119.3 F5220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr5:92923998 C>T maps to NM_005654.4 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr5:92923998 C>T maps to NM_005654.4 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr5:128302162 G>A maps to NM_001017372.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr5:128302162 G>A maps to NM_001017372.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr5:149562338 C>A maps to NM_001804.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr5:149562338 C>A maps to NM_001804.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr5:176709522 C>T maps to NM_022455.4 R1984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr5:176709522 C>T maps to NM_022455.4 R1984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr6:27778003 G>A maps to NM_003536.2 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr6:27778003 G>A maps to NM_003536.2 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr6:32947815 G>T maps to ENST00000395289 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr6:32947815 G>T maps to ENST00000395289 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr6:38885711 A>G maps to ENST00000327475 A3428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr6:38885711 A>G maps to ENST00000327475 A3428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr6:86324794 G>A maps to NM_006372.4 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr6:86324794 G>A maps to NM_006372.4 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr6:117198534 C>T maps to NM_173560.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr6:117198534 C>T maps to NM_173560.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr6:150263228 C>A maps to NM_025217.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr6:150263228 C>A maps to NM_025217.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr6:165862442 T>A maps to NM_001130690.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr6:165862442 T>A maps to NM_001130690.1 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr7:95157464 C>A maps to NM_016116.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr7:95157464 C>A maps to NM_016116.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr7:157959788 G>A maps to NM_002847.3 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr7:157959788 G>A maps to NM_002847.3 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr8:103236306 A>G maps to NM_015713.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr8:103236306 A>G maps to NM_015713.4 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr8:121256221 C>T maps to NM_021110.1 V818V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr8:121256221 C>T maps to NM_021110.1 V818V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr9:289551 C>T maps to NM_203447.3 Y125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr9:289551 C>T maps to NM_203447.3 Y125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr9:130482359 C>T maps to NM_144965.1 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr9:130482359 C>T maps to NM_144965.1 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr9:140330689 G>A maps to NM_001033113.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr9:140330689 G>A maps to NM_001033113.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chrX:30327171 C>A maps to NM_000475.4 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chrX:30327171 C>A maps to NM_000475.4 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chrX:132438793 G>A maps to NM_001448.2 N417N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chrX:132438793 G>A maps to NM_001448.2 N417N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr17:79892537 C>T maps to ENST00000432920 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr17:79892537 C>T maps to ENST00000432920 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr1:27216254 G>A maps to NM_018066.3 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr1:27216254 G>A maps to NM_018066.3 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr1:167409930 G>C maps to NM_198053.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr1:167409930 G>C maps to NM_198053.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr1:248513011 G>A maps to NM_001001918.1 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr1:248513011 G>A maps to NM_001001918.1 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr10:50820225 C>T maps to NM_003055.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr10:50820225 C>T maps to NM_003055.2 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr11:20119139 C>G maps to ENST00000396087 V2069V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr11:20119139 C>G maps to ENST00000396087 V2069V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr15:57732648 C>T maps to NM_032866.3 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr15:57732648 C>T maps to NM_032866.3 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr16:77465452 G>A maps to NM_199355.2 H78H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr16:77465452 G>A maps to NM_199355.2 H78H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr19:6040053 G>T maps to NM_000635.3 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr19:6040053 G>T maps to NM_000635.3 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr2:179599566 G>A maps to NM_133378.4 V3784V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr2:179599566 G>A maps to NM_133378.4 V3784V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr20:33876322 C>T maps to NM_178468.4 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr20:33876322 C>T maps to NM_178468.4 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr22:32003954 G>C maps to NM_001007467.1 V730V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr22:32003954 G>C maps to NM_001007467.1 V730V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr3:447202 G>T maps to NM_006614.2 G1162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr3:447202 G>T maps to NM_006614.2 G1162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr3:129247884 C>T maps to NM_000539.3 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr3:129247884 C>T maps to NM_000539.3 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr4:110667594 A>G maps to ENST00000394635 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr4:110667594 A>G maps to ENST00000394635 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr4:187521087 G>A maps to ENST00000260147 Q4026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr4:187521087 G>A maps to ENST00000260147 Q4026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr5:86659244 C>T maps to NM_002890.1 R512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr5:86659244 C>T maps to NM_002890.1 R512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr6:27839919 C>T maps to NM_003533.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr6:27839919 C>T maps to NM_003533.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr6:31847880 G>A maps to ENST00000395728 L1262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr6:31847880 G>A maps to ENST00000395728 L1262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr6:146755793 G>A maps to NM_000838.3 S1149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr6:146755793 G>A maps to NM_000838.3 S1149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr7:8790657 G>A maps to NM_152745.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr7:8790657 G>A maps to NM_152745.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr7:110763262 C>A maps to NM_018334.4 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr7:110763262 C>A maps to NM_018334.4 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chrX:68725655 C>A maps to NM_015686.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chrX:68725655 C>A maps to NM_015686.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chrX:99662704 C>A maps to NM_001184880.1 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chrX:99662704 C>A maps to NM_001184880.1 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr19:15905619 C>A maps to NM_001004466.1 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chr19:15905619 C>A maps to NM_001004466.1 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chrX:153059757 G>A maps to NM_004135.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6959-01A-11D-1912-08 chrX:153059757 G>A maps to NM_004135.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr1:11562934 C>T maps to NM_020780.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr1:11562934 C>T maps to NM_020780.1 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr1:22927548 T>C maps to NM_020526.3 P899P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr1:22927548 T>C maps to NM_020526.3 P899P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr1:103354186 C>A did not map to a codon.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr1:103354186 C>A did not map to a codon.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr1:218614595 C>A maps to NM_001135599.2 C407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr1:218614595 C>A maps to NM_001135599.2 C407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr10:14894528 A>T maps to NM_016299.2 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr10:14894528 A>T maps to NM_016299.2 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr10:62648783 C>T maps to NM_014836.4 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr10:62648783 C>T maps to NM_014836.4 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr11:5758675 C>T maps to NM_001005180.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr11:5758675 C>T maps to NM_001005180.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr11:6048914 G>T maps to NM_001001917.2 S7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr11:6048914 G>T maps to NM_001001917.2 S7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr11:26725199 G>A maps to NM_178498.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr11:26725199 G>A maps to NM_178498.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr11:67051731 G>A maps to NM_001619.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr11:67051731 G>A maps to NM_001619.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr11:113076801 C>A maps to ENST00000316851 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr11:113076801 C>A maps to ENST00000316851 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr11:117282543 G>A maps to NM_014956.4 S1399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr11:117282543 G>A maps to NM_014956.4 S1399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr12:11506583 G>T maps to NM_005039.3 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr12:11506583 G>T maps to NM_005039.3 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr12:114261055 G>A maps to NM_016196.3 D952D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr12:114261055 G>A maps to NM_016196.3 D952D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr13:107822852 C>A maps to NM_001080396.2 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr13:107822852 C>A maps to NM_001080396.2 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr14:51464788 G>A maps to ENST00000338969 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr14:51464788 G>A maps to ENST00000338969 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr14:62204928 G>A maps to ENST00000394997 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr14:62204928 G>A maps to ENST00000394997 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr14:89088974 A>G maps to ENST00000380664 D1662D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr14:89088974 A>G maps to ENST00000380664 D1662D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr14:93151467 G>A maps to NM_024832.3 K868K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr14:93151467 G>A maps to NM_024832.3 K868K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr15:29346998 C>T maps to NM_005503.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr15:29346998 C>T maps to NM_005503.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr16:48595683 A>G maps to NM_153029.3 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr16:48595683 A>G maps to NM_153029.3 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr16:84492911 C>T maps to ENST00000416219 T751T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr16:84492911 C>T maps to ENST00000416219 T751T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr17:30801832 A>G maps to NM_002815.2 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr17:30801832 A>G maps to NM_002815.2 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr18:23873439 C>T maps to ENST00000418698 Q598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr18:23873439 C>T maps to ENST00000418698 Q598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr19:9213868 C>T maps to NM_001005193.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr19:9213868 C>T maps to NM_001005193.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr2:3598054 G>A maps to NM_002936.3 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr2:3598054 G>A maps to NM_002936.3 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr2:37232866 C>A maps to NM_019024.1 E1605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr2:37232866 C>A maps to NM_019024.1 E1605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr2:43451841 C>A maps to NM_006887.4 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr2:43451841 C>A maps to NM_006887.4 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr2:88874651 G>A maps to NM_004836.5 H783H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr2:88874651 G>A maps to NM_004836.5 H783H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr2:136107558 C>A maps to NM_032143.2 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr2:136107558 C>A maps to NM_032143.2 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr2:238249122 G>A maps to NM_004369.3 F2812F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr2:238249122 G>A maps to NM_004369.3 F2812F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr20:3845383 C>T maps to NM_020746.3 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr20:3845383 C>T maps to NM_020746.3 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr21:22696775 C>T maps to NM_004540.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr21:22696775 C>T maps to NM_004540.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr3:30875410 G>T maps to NM_207359.2 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr3:30875410 G>T maps to NM_207359.2 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr3:49738098 C>T maps to NM_022064.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr3:49738098 C>T maps to NM_022064.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr3:74350819 C>A maps to NM_020872.1 V641V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr3:74350819 C>A maps to NM_020872.1 V641V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr3:164758777 A>G maps to NM_001041.3 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr3:164758777 A>G maps to NM_001041.3 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr3:180349271 G>T maps to NM_181426.1 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr3:180349271 G>T maps to NM_181426.1 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr4:13602127 G>T maps to NM_148894.2 A2132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr4:13602127 G>T maps to NM_148894.2 A2132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr4:81188292 G>T maps to NM_004464.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr4:81188292 G>T maps to NM_004464.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr4:100830006 T>C maps to NM_001031723.2 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr4:100830006 T>C maps to NM_001031723.2 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr5:10992675 G>T maps to NM_001332.2 P1066P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr5:10992675 G>T maps to NM_001332.2 P1066P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr5:153056595 G>T maps to NM_001114183.1 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr5:153056595 G>T maps to NM_001114183.1 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr5:167921570 C>T maps to NM_002887.3 H165H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr5:167921570 C>T maps to NM_002887.3 H165H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr6:42936616 G>A maps to NM_000287.3 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr6:42936616 G>A maps to NM_000287.3 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr6:130378575 G>T maps to NM_032438.2 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr6:130378575 G>T maps to NM_032438.2 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr7:32209515 C>A maps to NM_001191058.1 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr7:32209515 C>A maps to NM_001191058.1 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr7:97872808 C>A maps to ENST00000379795 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr7:97872808 C>A maps to ENST00000379795 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr7:100685832 C>T maps to NM_001040105.1 S3712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr7:100685832 C>T maps to NM_001040105.1 S3712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr7:103216152 C>A did not map to a codon.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr7:103216152 C>A did not map to a codon.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr7:142750109 C>A maps to NM_001001667.1 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr7:142750109 C>A maps to NM_001001667.1 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr8:48649938 C>A maps to NM_005195.3 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr8:48649938 C>A maps to NM_005195.3 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr8:68184171 C>A did not map to a codon.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr8:68184171 C>A did not map to a codon.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr8:95863868 A>G maps to NM_017864.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr8:95863868 A>G maps to NM_017864.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr9:108366710 T>A maps to NM_006731.2 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr9:108366710 T>A maps to NM_006731.2 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr9:140438231 A>C maps to NM_001098537.1 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chr9:140438231 A>C maps to NM_001098537.1 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chrX:110653365 C>G maps to ENST00000358070 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chrX:110653365 C>G maps to ENST00000358070 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chrX:138899027 G>A maps to NM_173694.4 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chrX:138899027 G>A maps to NM_173694.4 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chrX:144329126 C>T maps to NM_001009614.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6960-01A-41D-2012-08 chrX:144329126 C>T maps to NM_001009614.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:1019466 C>T maps to ENST00000448924 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:1019466 C>T maps to ENST00000448924 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:15983118 G>A maps to NM_032341.4 Q397Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:15983118 G>A maps to NM_032341.4 Q397Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:43907766 G>A maps to NM_015284.2 R1714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:43907766 G>A maps to NM_015284.2 R1714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:45120815 G>T maps to NM_024587.2 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:45120815 G>T maps to NM_024587.2 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:45295678 C>G maps to NM_003738.4 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:45295678 C>G maps to NM_003738.4 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:46745254 C>T maps to ENST00000254454 E662E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:46745254 C>T maps to ENST00000254454 E662E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:55081831 G>T maps to NM_176782.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:55081831 G>T maps to NM_176782.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:94337702 C>T maps to NM_014597.4 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:94337702 C>T maps to NM_014597.4 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:109191449 G>C maps to ENST00000370031 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:109191449 G>C maps to ENST00000370031 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:109461320 G>A maps to NM_013296.4 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:109461320 G>A maps to NM_013296.4 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:116577933 G>A maps to NM_018420.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:116577933 G>A maps to NM_018420.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:145368590 C>T maps to NM_001039703.4 I3523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:145368590 C>T maps to NM_001039703.4 I3523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:152732721 C>T maps to NM_001025231.1 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:152732721 C>T maps to NM_001025231.1 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:153580540 G>C maps to NM_080388.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:153580540 G>C maps to NM_080388.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:153661437 C>T maps to NM_000906.3 S809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:153661437 C>T maps to NM_000906.3 S809S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:154246315 C>G maps to NM_006118.3 S128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:154246315 C>G maps to NM_006118.3 S128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:155295460 C>T maps to NM_001105203.1 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:155295460 C>T maps to NM_001105203.1 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:160970526 G>A maps to NM_016946.4 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:160970526 G>A maps to NM_016946.4 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:161199673 C>G maps to NM_001077482.1 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:161199673 C>G maps to NM_001077482.1 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:161476259 C>G maps to NM_001136219.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:161476259 C>G maps to NM_001136219.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:186370310 G>C maps to NM_022375.3 *45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:186370310 G>C maps to NM_022375.3 *45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:193150248 C>T maps to NM_003783.3 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:193150248 C>T maps to NM_003783.3 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:205779419 C>G maps to NM_173854.4 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:205779419 C>G maps to NM_173854.4 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:210334215 G>A maps to NM_001146261.1 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:210334215 G>A maps to NM_001146261.1 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:216850529 G>A maps to NM_001438.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:216850529 G>A maps to NM_001438.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:219384872 C>T maps to NM_138794.3 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:219384872 C>T maps to NM_138794.3 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:235345583 C>A maps to NM_016374.5 E884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:235345583 C>A maps to NM_016374.5 E884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:247694955 C>G maps to NM_198074.4 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr1:247694955 C>G maps to NM_198074.4 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:14280916 G>A maps to NM_006108.2 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:14280916 G>A maps to NM_006108.2 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:14486568 C>T maps to NM_001144061.1 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:14486568 C>T maps to NM_001144061.1 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:33566370 G>A maps to ENST00000389726 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:33566370 G>A maps to ENST00000389726 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:57069956 G>A maps to NM_033396.2 P1553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:57069956 G>A maps to NM_033396.2 P1553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:61548769 C>T maps to NM_001127392.1 S911S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:61548769 C>T maps to NM_001127392.1 S911S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:72409007 G>A maps to NM_001040118.2 F895F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:72409007 G>A maps to NM_001040118.2 F895F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:76873900 C>T maps to NM_000260.3 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:76873900 C>T maps to NM_000260.3 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:123886937 C>A maps to NM_001004462.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:123886937 C>A maps to NM_001004462.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:7054985 G>A maps to NM_138425.2 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:7054985 G>A maps to NM_138425.2 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:7260990 C>T maps to NM_016546.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:7260990 C>T maps to NM_016546.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:14959194 G>A maps to NM_001013698.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:14959194 G>A maps to NM_001013698.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:21358888 C>G maps to NM_006446.4 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:21358888 C>G maps to NM_006446.4 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:50035743 C>T maps to NM_001031698.1 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:50035743 C>T maps to NM_001031698.1 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:55688557 G>A maps to NM_001005493.1 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:55688557 G>A maps to NM_001005493.1 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:56740693 C>A maps to NM_005419.3 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:56740693 C>A maps to NM_005419.3 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:57106605 C>T maps to NM_001113203.1 L2062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:57106605 C>T maps to NM_001113203.1 L2062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:57108148 C>A maps to NM_001113203.1 R1940R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:57108148 C>A maps to NM_001113203.1 R1940R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:57484985 C>A maps to NM_005967.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:57484985 C>A maps to NM_005967.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:85500376 C>T maps to NM_001079910.1 Q1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:85500376 C>T maps to NM_001079910.1 Q1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:91358090 G>A maps to NM_004950.4 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:91358090 G>A maps to NM_004950.4 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:120635241 G>C maps to NM_053275.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:120635241 G>C maps to NM_053275.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:122958595 C>T maps to NM_017612.2 Q524Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:122958595 C>T maps to NM_017612.2 Q524Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:124298072 C>G maps to NM_207437.3 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr12:124298072 C>G maps to NM_207437.3 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr13:25348971 A>C maps to ENST00000381927 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr13:25348971 A>C maps to ENST00000381927 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr13:33703292 G>T maps to NM_178007.2 V499V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr13:33703292 G>T maps to NM_178007.2 V499V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr13:47466710 G>A maps to NM_000621.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr13:47466710 G>A maps to NM_000621.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr13:100622423 G>A maps to NM_033132.3 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr13:100622423 G>A maps to NM_033132.3 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:23523751 G>C maps to NM_022478.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:23523751 G>C maps to NM_022478.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:39716594 C>T maps to NM_054024.3 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:39716594 C>T maps to NM_054024.3 Q273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:64746789 G>A maps to NM_001437.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:64746789 G>A maps to NM_001437.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:79432617 G>A maps to NM_004796.4 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:79432617 G>A maps to NM_004796.4 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:92469777 C>T maps to NM_004239.3 L1514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:92469777 C>T maps to NM_004239.3 L1514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:92469840 C>T maps to NM_004239.3 L1493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:92469840 C>T maps to NM_004239.3 L1493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:92471130 C>T maps to NM_004239.3 Q1063Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:92471130 C>T maps to NM_004239.3 Q1063Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:100743852 C>T maps to NM_003403.3 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:100743852 C>T maps to NM_003403.3 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:105716078 C>T maps to NM_033271.2 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr14:105716078 C>T maps to NM_033271.2 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:22850971 C>T maps to NM_052903.4 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:22850971 C>T maps to NM_052903.4 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:72460094 G>T maps to NM_001012642.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:72460094 G>T maps to NM_001012642.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:72582527 G>A maps to NM_052840.4 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:72582527 G>A maps to NM_052840.4 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:83518565 C>T maps to NM_199330.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:83518565 C>T maps to NM_199330.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:83687527 G>A maps to NM_025238.3 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:83687527 G>A maps to NM_025238.3 F407F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:85407690 G>A maps to NM_020778.4 L1708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:85407690 G>A maps to NM_020778.4 L1708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:91448543 G>T maps to NM_006122.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:91448543 G>T maps to NM_006122.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:99459286 G>C maps to NM_000875.3 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr15:99459286 G>C maps to NM_000875.3 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:5112510 G>A maps to ENST00000350219 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:5112510 G>A maps to ENST00000350219 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:8875250 C>A maps to NM_001127448.1 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:8875250 C>A maps to NM_001127448.1 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:19659192 C>T maps to NM_020314.5 Q762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:19659192 C>T maps to NM_020314.5 Q762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:28997454 G>C did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:28997454 G>C did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:31213942 G>A maps to NM_013258.4 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:31213942 G>A maps to NM_013258.4 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:68961607 C>A maps to NM_024562.1 A755A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:68961607 C>A maps to NM_024562.1 A755A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:71512137 G>A maps to NM_006961.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:71512137 G>A maps to NM_006961.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:81078337 C>G maps to NM_015251.2 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:81078337 C>G maps to NM_015251.2 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:89930014 G>T maps to NM_032451.1 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:89930014 G>T maps to NM_032451.1 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:4009036 G>C maps to NM_015113.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:4009036 G>C maps to NM_015113.3 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:12823100 G>A maps to NM_014859.4 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:12823100 G>A maps to NM_014859.4 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:17398762 G>A maps to NM_016084.3 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:17398762 G>A maps to NM_016084.3 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:17921886 G>C maps to NM_145691.3 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:17921886 G>C maps to NM_145691.3 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:27244464 C>G maps to NM_001033561.1 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:27244464 C>G maps to NM_001033561.1 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:37842183 G>A maps to NM_033419.3 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:37842183 G>A maps to NM_033419.3 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:46685394 C>A maps to NM_004502.3 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:46685394 C>A maps to NM_004502.3 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:66548054 C>T maps to NM_017565.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:66548054 C>T maps to NM_017565.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:74018541 C>T maps to NM_001988.2 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:74018541 C>T maps to NM_001988.2 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:76455097 G>A maps to ENST00000389840 I3268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:76455097 G>A maps to ENST00000389840 I3268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:78358942 C>T maps to NM_020914.4 I4858I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:78358942 C>T maps to NM_020914.4 I4858I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:79916265 G>A maps to NM_178493.5 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:79916265 G>A maps to NM_178493.5 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr18:12028873 C>T maps to NM_014214.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr18:12028873 C>T maps to NM_014214.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr18:19429230 C>G maps to NM_020774.2 S823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr18:19429230 C>G maps to NM_020774.2 S823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr18:19761412 G>A did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr18:19761412 G>A did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr18:46906125 C>A maps to NM_017653.3 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr18:46906125 C>A maps to NM_017653.3 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr18:67801734 G>A maps to NM_173630.3 F976F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr18:67801734 G>A maps to NM_173630.3 F976F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:873568 G>C maps to NM_005481.2 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:873568 G>C maps to NM_005481.2 V595V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:1585104 C>T maps to NM_003926.5 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:1585104 C>T maps to NM_003926.5 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:9011340 C>T maps to NM_024690.2 R12964R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:9011340 C>T maps to NM_024690.2 R12964R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:12060473 C>T maps to NM_144566.1 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:12060473 C>T maps to NM_144566.1 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:13247197 G>T maps to NM_052876.2 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:13247197 G>T maps to NM_052876.2 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:14000823 G>C maps to ENST00000454313 S282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:14000823 G>C maps to ENST00000454313 S282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:14020718 C>T maps to NM_017721.4 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:14020718 C>T maps to NM_017721.4 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:18543508 G>C did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:18543508 G>C did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:33183198 G>A maps to NM_001105570.1 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:33183198 G>A maps to NM_001105570.1 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:35502415 C>T maps to NM_020895.3 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:35502415 C>T maps to NM_020895.3 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:36037924 C>T maps to NM_032635.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:36037924 C>T maps to NM_032635.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:39103252 G>A maps to NM_001042600.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:39103252 G>A maps to NM_001042600.1 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:41125250 G>A did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:41125250 G>A did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:41630771 C>T maps to NM_000774.3 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:41630771 C>T maps to NM_000774.3 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:48185360 C>T maps to NM_015711.3 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:48185360 C>T maps to NM_015711.3 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:51410249 A>C maps to NM_004917.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:51410249 A>C maps to NM_004917.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:52793883 C>T maps to NM_001010851.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:52793883 C>T maps to NM_001010851.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:54744932 G>A maps to ENST00000245620 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:54744932 G>A maps to ENST00000245620 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:55401036 G>A maps to NM_002000.2 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr19:55401036 G>A maps to NM_002000.2 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:27463929 G>A maps to NM_004341.3 L1881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:27463929 G>A maps to NM_004341.3 L1881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:85628365 C>T maps to NM_001747.2 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:85628365 C>T maps to NM_001747.2 K146K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:136399346 C>T maps to ENST00000409606 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:136399346 C>T maps to ENST00000409606 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:166900255 C>A maps to NM_001165963.1 G656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:166900255 C>A maps to NM_001165963.1 G656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:182763788 G>A maps to NM_001130445.1 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:182763788 G>A maps to NM_001130445.1 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:219000409 C>T maps to NM_001168298.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:219000409 C>T maps to NM_001168298.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:220101165 G>A maps to NM_001042410.1 *727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:220101165 G>A maps to NM_001042410.1 *727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:220412741 C>T maps to NM_001005209.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr2:220412741 C>T maps to NM_001005209.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:428598 C>A maps to ENST00000246077 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:428598 C>A maps to ENST00000246077 E89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:2560665 T>A maps to NM_080751.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:2560665 T>A maps to NM_080751.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:4705247 C>G maps to NM_012409.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:4705247 C>G maps to NM_012409.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:18724747 C>G maps to NM_080820.4 S161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:18724747 C>G maps to NM_080820.4 S161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:33567490 C>T maps to NM_020884.3 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:33567490 C>T maps to NM_020884.3 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:34054792 C>T maps to NM_007186.3 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:34054792 C>T maps to NM_007186.3 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:43964467 G>A maps to NM_002999.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:43964467 G>A maps to NM_002999.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:50140539 G>A maps to NM_012340.3 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:50140539 G>A maps to NM_012340.3 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:62298845 G>C maps to ENST00000482936 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:62298845 G>C maps to ENST00000482936 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr21:31709485 G>A maps to NM_001077711.1 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr21:31709485 G>A maps to NM_001077711.1 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr21:40194811 G>T maps to NM_005239.4 *470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr21:40194811 G>T maps to NM_005239.4 *470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr21:45959217 G>A maps to NM_198691.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr21:45959217 G>A maps to NM_198691.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:17288750 G>A maps to NM_175878.3 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:17288750 G>A maps to NM_175878.3 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:21107309 C>T maps to NM_058004.2 K898K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:21107309 C>T maps to NM_058004.2 K898K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:24086060 G>A maps to NM_021916.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:24086060 G>A maps to NM_021916.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:24086775 G>C maps to NM_021916.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:24086775 G>C maps to NM_021916.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:32587229 C>T maps to NM_001098527.2 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:32587229 C>T maps to NM_001098527.2 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:41738567 C>T maps to ENST00000351589 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:41738567 C>T maps to ENST00000351589 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:50654233 G>A maps to NM_031454.1 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr22:50654233 G>A maps to NM_031454.1 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:9517532 C>T maps to ENST00000407969 Q1382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:9517532 C>T maps to ENST00000407969 Q1382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:9979761 C>T maps to NM_001077415.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:9979761 C>T maps to NM_001077415.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:30691946 C>G maps to NM_001024847.2 S175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:30691946 C>G maps to NM_001024847.2 S175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:48789026 G>A maps to NM_004157.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:48789026 G>A maps to NM_004157.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:49702265 C>T maps to NM_003458.3 F3925F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:49702265 C>T maps to NM_003458.3 F3925F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:97887884 C>G maps to NM_001005515.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:97887884 C>G maps to NM_001005515.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:99881148 G>A maps to NM_032359.3 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:99881148 G>A maps to NM_032359.3 K76K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:112358404 C>T maps to ENST00000447230 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:112358404 C>T maps to ENST00000447230 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:127327233 C>T maps to NM_004526.2 Q371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:127327233 C>T maps to NM_004526.2 Q371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:155200496 C>T maps to ENST00000340059 E1114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:155200496 C>T maps to ENST00000340059 E1114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:169802026 C>T maps to NM_014373.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:169802026 C>T maps to NM_014373.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:183900580 C>T maps to ENST00000411763 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:183900580 C>T maps to ENST00000411763 I391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:194309350 C>G maps to NM_001166305.1 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr3:194309350 C>G maps to NM_001166305.1 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr4:39448238 G>A maps to NM_175737.3 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr4:39448238 G>A maps to NM_175737.3 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr4:78079753 C>G maps to NM_004354.2 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr4:78079753 C>G maps to NM_004354.2 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr4:79455675 C>T maps to NM_025074.6 Q3667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr4:79455675 C>T maps to NM_025074.6 Q3667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr4:122078302 C>T maps to ENST00000509841 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr4:122078302 C>T maps to ENST00000509841 Q180Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr4:151773392 G>A maps to NM_006726.3 Q1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr4:151773392 G>A maps to NM_006726.3 Q1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr4:159791563 C>T maps to ENST00000379346 T987T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr4:159791563 C>T maps to ENST00000379346 T987T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr4:174254785 G>A maps to NM_002129.3 D5D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr4:174254785 G>A maps to NM_002129.3 D5D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:5306807 G>A maps to NM_139056.2 S1126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:5306807 G>A maps to NM_139056.2 S1126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:36686316 G>A maps to NM_004172.4 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:36686316 G>A maps to NM_004172.4 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:70786859 G>A maps to NM_018429.2 K514K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:70786859 G>A maps to NM_018429.2 K514K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:79029811 C>T maps to NM_153610.3 Q1742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:79029811 C>T maps to NM_153610.3 Q1742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:90074288 C>T maps to NM_032119.3 Q4238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:90074288 C>T maps to NM_032119.3 Q4238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:112889015 C>T maps to NM_022828.3 I609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:112889015 C>T maps to NM_022828.3 I609I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:137045499 C>T maps to NM_017415.2 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:137045499 C>T maps to NM_017415.2 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:149576345 C>G maps to NM_014228.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:149576345 C>G maps to NM_014228.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:153760020 G>A maps to NM_198321.3 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:153760020 G>A maps to NM_198321.3 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:178507031 C>T maps to NM_014594.1 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr5:178507031 C>T maps to NM_014594.1 F533F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr6:16141927 G>T maps to NM_013262.3 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr6:16141927 G>T maps to NM_013262.3 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr6:36285133 C>T maps to NM_001010903.4 *653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr6:36285133 C>T maps to NM_001010903.4 *653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr6:84311157 C>G did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr6:84311157 C>G did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr6:90402812 C>T maps to NM_014611.1 K3312K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr6:90402812 C>T maps to NM_014611.1 K3312K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr6:109285455 C>T maps to NM_032131.4 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr6:109285455 C>T maps to NM_032131.4 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:14613863 G>A maps to NM_004080.2 I582I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:14613863 G>A maps to NM_004080.2 I582I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:19156445 C>A maps to NM_000474.3 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:19156445 C>A maps to NM_000474.3 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:20739703 G>T maps to NM_001163941.1 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:20739703 G>T maps to NM_001163941.1 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:21639529 G>A maps to NM_003777.3 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:21639529 G>A maps to NM_003777.3 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:44578909 C>T maps to NM_013389.2 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:44578909 C>T maps to NM_013389.2 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:98545956 G>C maps to ENST00000359863 L1547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:98545956 G>C maps to ENST00000359863 L1547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:99696308 G>A maps to NM_005916.3 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:99696308 G>A maps to NM_005916.3 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:99710523 C>T maps to ENST00000472509 Q214Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:99710523 C>T maps to ENST00000472509 Q214Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:127236416 C>T maps to NM_020369.2 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:127236416 C>T maps to NM_020369.2 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:138603405 G>A maps to NM_001164665.1 Y322Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr7:138603405 G>A maps to NM_001164665.1 Y322Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:22210624 C>T maps to NM_001135721.1 Q853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:22210624 C>T maps to NM_001135721.1 Q853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:22494438 G>A maps to NM_018688.4 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:22494438 G>A maps to NM_018688.4 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:22886090 G>T maps to NM_003842.4 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:22886090 G>T maps to NM_003842.4 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:35616847 C>G maps to ENST00000416672 S730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:35616847 C>G maps to ENST00000416672 S730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:38162180 G>A maps to NM_023034.1 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:38162180 G>A maps to NM_023034.1 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:42693173 G>A maps to NM_018105.2 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:42693173 G>A maps to NM_018105.2 D191D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:43048964 G>A maps to ENST00000458501 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:43048964 G>A maps to ENST00000458501 V509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:95508621 T>C maps to NM_015496.3 K1439K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:95508621 T>C maps to NM_015496.3 K1439K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:95942724 C>T maps to NM_033285.3 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:95942724 C>T maps to NM_033285.3 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:124810475 C>T maps to NM_144963.2 Q520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:124810475 C>T maps to NM_144963.2 Q520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:125989716 C>T maps to NM_152412.2 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:125989716 C>T maps to NM_152412.2 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:143961151 C>G maps to ENST00000377675 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:143961151 C>G maps to ENST00000377675 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:144991748 C>T maps to NM_201380.2 L4217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:144991748 C>T maps to NM_201380.2 L4217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:145007121 G>A maps to NM_201380.2 Q663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr8:145007121 G>A maps to NM_201380.2 Q663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr9:33796722 G>A maps to NM_007343.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr9:33796722 G>A maps to NM_007343.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr9:116083792 G>A maps to NM_001012361.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr9:116083792 G>A maps to NM_001012361.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr9:139749722 G>A maps to ENST00000392881 Q405Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr9:139749722 G>A maps to ENST00000392881 Q405Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chrX:46472744 C>G maps to NM_032591.1 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chrX:46472744 C>G maps to NM_032591.1 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chrX:47485838 G>A maps to NM_002621.2 I340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chrX:47485838 G>A maps to NM_002621.2 I340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chrX:115585605 C>T maps to NM_007231.3 Q468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chrX:115585605 C>T maps to NM_007231.3 Q468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chrX:151870253 G>C maps to NM_005363.2 *315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chrX:151870253 G>C maps to NM_005363.2 *315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chrX:153760232 C>A maps to ENST00000369620 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chrX:153760232 C>A maps to ENST00000369620 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:111983 G>A maps to NM_022450.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:111983 G>A maps to NM_022450.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:69874158 G>C maps to NM_007014.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr16:69874158 G>C maps to NM_007014.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr18:60212053 C>G maps to NM_017742.4 S383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr18:60212053 C>G maps to NM_017742.4 S383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:60942118 G>A maps to NM_005560.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr20:60942118 G>A maps to NM_005560.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chrX:70470283 C>T maps to ENST00000373988 K359K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chrX:70470283 C>T maps to ENST00000373988 K359K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr1:12304643 C>A maps to NM_015378.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr1:12304643 C>A maps to NM_015378.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr1:17668882 G>A maps to NM_012387.2 E307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr1:17668882 G>A maps to NM_012387.2 E307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr1:65301897 C>T maps to NM_002227.2 W1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr1:65301897 C>T maps to NM_002227.2 W1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr1:109170787 G>C did not map to a codon.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr1:109170787 G>C did not map to a codon.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr1:167865863 G>A maps to NM_018417.4 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr1:167865863 G>A maps to NM_018417.4 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr10:33199208 A>C maps to ENST00000374956 Y702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr10:33199208 A>C maps to ENST00000374956 Y702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr10:48388213 G>T maps to NM_002900.2 P888P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr10:48388213 G>T maps to NM_002900.2 P888P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr11:55432770 T>C maps to NM_001004704.1 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr11:55432770 T>C maps to NM_001004704.1 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr11:55861496 C>A maps to NM_001003750.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr11:55861496 C>A maps to NM_001003750.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr11:64577226 T>A maps to NM_130804.2 K119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr11:64577226 T>A maps to NM_130804.2 K119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr12:11421067 G>A maps to NM_006249.4 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr12:11421067 G>A maps to NM_006249.4 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr12:53662896 C>A maps to NM_012291.4 C57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr12:53662896 C>A maps to NM_012291.4 C57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr12:98931316 A>T maps to NM_001032283.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr12:98931316 A>T maps to NM_001032283.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr14:73404778 G>A did not map to a codon.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr14:73404778 G>A did not map to a codon.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr16:22134932 G>T did not map to a codon.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr16:22134932 G>T did not map to a codon.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr17:30668272 G>A maps to NM_022344.2 D57D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr17:30668272 G>A maps to NM_022344.2 D57D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr17:40734007 C>A maps to NM_178126.3 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr17:40734007 C>A maps to NM_178126.3 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr17:72613587 C>T maps to ENST00000426295 K60K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr17:72613587 C>T maps to ENST00000426295 K60K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr18:21703802 C>T maps to NM_001135993.1 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr18:21703802 C>T maps to NM_001135993.1 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:4365607 G>A maps to NM_003025.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:4365607 G>A maps to NM_003025.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:11943140 C>T maps to NM_152357.2 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:11943140 C>T maps to NM_152357.2 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:21132174 C>A maps to NM_003429.4 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:21132174 C>A maps to NM_003429.4 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:36037858 A>G maps to NM_032635.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:36037858 A>G maps to NM_032635.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:39013682 G>A maps to NM_000540.2 T3425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:39013682 G>A maps to NM_000540.2 T3425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:39361465 C>T maps to NM_001195833.1 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:39361465 C>T maps to NM_001195833.1 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:59068276 C>T maps to NM_003969.3 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:59068276 C>T maps to NM_003969.3 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr21:11098869 C>A did not map to a codon.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr21:11098869 C>A did not map to a codon.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr3:171431701 G>A maps to NM_002662.3 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr3:171431701 G>A maps to NM_002662.3 R298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr3:185986616 C>T maps to NM_001346.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr3:185986616 C>T maps to NM_001346.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr5:128796152 C>T maps to NM_133638.3 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr5:128796152 C>T maps to NM_133638.3 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr7:5391492 C>T maps to NM_001080495.2 A1809A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr7:5391492 C>T maps to NM_001080495.2 A1809A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr7:24874173 G>A maps to NM_015550.2 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr7:24874173 G>A maps to NM_015550.2 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr7:43503398 G>A did not map to a codon.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr7:43503398 G>A did not map to a codon.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr7:107234421 A>G maps to NM_001008405.2 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr7:107234421 A>G maps to NM_001008405.2 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr7:150325294 G>A maps to ENST00000438845 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr7:150325294 G>A maps to ENST00000438845 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr8:23243521 A>T maps to ENST00000356206 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr8:23243521 A>T maps to ENST00000356206 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr8:110099851 C>A maps to NM_003301.4 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr8:110099851 C>A maps to NM_003301.4 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr9:21971028 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr9:21971028 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chrX:35966560 A>G maps to NM_152632.3 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chrX:35966560 A>G maps to NM_152632.3 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chrX:119421059 G>T maps to NM_017938.3 Y124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chrX:119421059 G>T maps to NM_017938.3 Y124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chrX:140785696 T>C maps to NM_145665.1 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chrX:140785696 T>C maps to NM_145665.1 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:1011794 C>T maps to NM_001033026.1 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6962-01A-11D-1912-08 chr19:1011794 C>T maps to NM_001033026.1 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr1:19632583 G>A maps to NM_003689.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr1:19632583 G>A maps to NM_003689.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr1:21800025 C>T maps to NM_032264.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr1:21800025 C>T maps to NM_032264.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr1:44424509 T>C maps to NM_014652.3 D659D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr1:44424509 T>C maps to NM_014652.3 D659D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr1:158817561 T>C maps to NM_002432.1 N344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr1:158817561 T>C maps to NM_002432.1 N344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr1:215823957 G>A maps to ENST00000366943 S4773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr1:215823957 G>A maps to ENST00000366943 S4773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr10:87966142 G>T maps to NM_017551.2 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr10:87966142 G>T maps to NM_017551.2 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr11:55761663 G>A maps to NM_003697.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr11:55761663 G>A maps to NM_003697.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr11:58891900 C>T maps to NM_198947.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr11:58891900 C>T maps to NM_198947.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr11:59224762 A>G maps to NM_001004708.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr11:59224762 A>G maps to NM_001004708.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr11:132016252 G>A maps to NM_001144058.1 W82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr11:132016252 G>A maps to NM_001144058.1 W82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr12:48888619 G>A maps to NM_152319.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr12:48888619 G>A maps to NM_152319.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr12:52309042 G>A maps to NM_001077401.1 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr12:52309042 G>A maps to NM_001077401.1 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr12:95603435 G>A maps to NM_018351.3 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr12:95603435 G>A maps to NM_018351.3 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr12:107415888 T>C maps to NM_004075.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr12:107415888 T>C maps to NM_004075.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr12:122991392 C>T maps to NM_023012.5 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr12:122991392 C>T maps to NM_023012.5 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr14:64564716 A>G maps to NM_182914.2 K4053K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr14:64564716 A>G maps to NM_182914.2 K4053K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr16:15130130 G>A maps to NM_015027.2 *789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr16:15130130 G>A maps to NM_015027.2 *789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr16:50348222 C>A maps to NM_001114.3 A959A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr16:50348222 C>A maps to NM_001114.3 A959A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr17:39122955 G>A maps to NM_213656.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr17:39122955 G>A maps to NM_213656.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr17:48148224 C>T maps to NM_002204.2 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr17:48148224 C>T maps to NM_002204.2 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr17:56397484 G>T maps to NM_004758.2 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr17:56397484 G>T maps to NM_004758.2 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr17:79991360 C>T maps to NM_005052.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr17:79991360 C>T maps to NM_005052.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr17:79991598 C>G maps to NM_005052.2 S158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr17:79991598 C>G maps to NM_005052.2 S158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr19:2110167 C>T maps to ENST00000355272 Q1077Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr19:2110167 C>T maps to ENST00000355272 Q1077Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr19:11532485 G>A maps to NM_145045.4 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr19:11532485 G>A maps to NM_145045.4 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr19:16025611 C>T maps to NM_021187.3 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr19:16025611 C>T maps to NM_021187.3 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr19:40366538 C>T maps to NM_003890.2 Q4565Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr19:40366538 C>T maps to NM_003890.2 Q4565Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr19:44160640 T>C maps to NM_002659.2 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr19:44160640 T>C maps to NM_002659.2 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr2:95941258 G>T did not map to a codon.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr2:95941258 G>T did not map to a codon.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr22:46652484 C>T maps to NM_006071.1 G2245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr22:46652484 C>T maps to NM_006071.1 G2245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr22:46654044 C>T maps to NM_006071.1 L1725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr22:46654044 C>T maps to NM_006071.1 L1725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr22:46654119 C>T maps to NM_006071.1 K1700K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr22:46654119 C>T maps to NM_006071.1 K1700K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr3:52623228 G>C maps to ENST00000296302 S941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr3:52623228 G>C maps to ENST00000296302 S941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr3:183778118 C>G maps to NM_130770.2 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr3:183778118 C>G maps to NM_130770.2 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr3:194118030 C>G maps to NM_004488.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr3:194118030 C>G maps to NM_004488.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr4:1360142 C>T maps to NM_020894.2 D404D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr4:1360142 C>T maps to NM_020894.2 D404D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr4:123230491 A>G maps to NM_015312.3 A3375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr4:123230491 A>G maps to NM_015312.3 A3375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr4:187541759 C>A maps to ENST00000260147 E1997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr4:187541759 C>A maps to ENST00000260147 E1997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr5:131819735 G>A maps to NM_002198.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr5:131819735 G>A maps to NM_002198.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr6:32974912 G>A maps to NM_002119.3 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr6:32974912 G>A maps to NM_002119.3 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr6:126334220 C>T maps to NM_001031712.2 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr6:126334220 C>T maps to NM_001031712.2 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr6:167704888 C>A did not map to a codon.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr6:167704888 C>A did not map to a codon.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr7:34125425 C>G maps to NM_133468.3 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr7:34125425 C>G maps to NM_133468.3 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr7:100345254 A>G maps to ENST00000349350 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr7:100345254 A>G maps to ENST00000349350 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr8:73849038 C>T maps to NM_004770.2 D483D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr8:73849038 C>T maps to NM_004770.2 D483D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr8:94746868 A>G maps to NM_203390.2 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr8:94746868 A>G maps to NM_203390.2 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr8:146067675 C>G maps to ENST00000446747 S405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr8:146067675 C>G maps to ENST00000446747 S405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr9:32632973 G>A maps to NM_153809.2 C868C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr9:32632973 G>A maps to NM_153809.2 C868C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr9:35231141 G>A maps to ENST00000396787 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr9:35231141 G>A maps to ENST00000396787 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr9:99581235 G>A maps to NM_001001662.1 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr9:99581235 G>A maps to NM_001001662.1 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr9:127990195 G>T maps to NM_005833.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr9:127990195 G>T maps to NM_005833.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chrX:18192279 A>C maps to NM_153346.4 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chrX:18192279 A>C maps to NM_153346.4 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chrX:135862906 G>A maps to NM_004840.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chrX:135862906 G>A maps to NM_004840.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr6:16143385 G>T maps to NM_013262.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7089-01A-11D-2012-08 chr6:16143385 G>T maps to NM_013262.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr1:27099012 G>C maps to NM_006015.4 G1143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr1:27099012 G>C maps to NM_006015.4 G1143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr1:60381633 G>A maps to NM_000775.2 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr1:60381633 G>A maps to NM_000775.2 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr1:170961469 G>A maps to NM_001163629.1 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr1:170961469 G>A maps to NM_001163629.1 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr11:28318420 C>T maps to NM_001113528.1 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr11:28318420 C>T maps to NM_001113528.1 Q241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr12:70974930 A>G maps to NM_001109754.1 S821S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr12:70974930 A>G maps to NM_001109754.1 S821S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr16:90001359 C>T maps to ENST00000304984 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr16:90001359 C>T maps to ENST00000304984 F514F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr17:48745370 G>A did not map to a codon.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr17:48745370 G>A did not map to a codon.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr18:20833869 C>G maps to NM_001100619.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr18:20833869 C>G maps to NM_001100619.2 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr19:10476498 C>G maps to NM_003331.4 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr19:10476498 C>G maps to NM_003331.4 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr19:44833907 G>A maps to ENST00000412927 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr19:44833907 G>A maps to ENST00000412927 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr20:9546620 G>A maps to NM_177990.2 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr20:9546620 G>A maps to NM_177990.2 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr3:86028419 C>A maps to NM_153184.3 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr3:86028419 C>A maps to NM_153184.3 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr3:160025458 G>A maps to ENST00000483754 Y527Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr3:160025458 G>A maps to ENST00000483754 Y527Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr4:367158 C>T maps to NM_003441.2 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr4:367158 C>T maps to NM_003441.2 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr4:155489612 A>T maps to NM_005141.4 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr4:155489612 A>T maps to NM_005141.4 R267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr6:133783831 C>A maps to ENST00000452339 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr6:133783831 C>A maps to ENST00000452339 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr7:20725390 C>T maps to NM_001163941.1 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr7:20725390 C>T maps to NM_001163941.1 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr7:33390924 C>G maps to NM_198428.2 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr7:33390924 C>G maps to NM_198428.2 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr9:139700964 C>T maps to NM_001039374.4 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chr9:139700964 C>T maps to NM_001039374.4 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chrX:79282318 C>A maps to NM_016954.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7090-01A-11D-2012-08 chrX:79282318 C>A maps to NM_016954.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr1:154029335 C>T maps to NM_207308.2 K1065K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr1:154029335 C>T maps to NM_207308.2 K1065K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr1:237060419 T>C did not map to a codon.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr1:237060419 T>C did not map to a codon.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr11:2594161 C>T maps to NM_000218.2 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr11:2594161 C>T maps to NM_000218.2 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr11:65631091 G>C maps to NM_025128.4 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr11:65631091 G>C maps to NM_025128.4 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr11:67821472 C>T maps to NM_001277.2 K452K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr11:67821472 C>T maps to NM_001277.2 K452K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr12:46592497 T>C maps to NM_030674.3 K344K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr12:46592497 T>C maps to NM_030674.3 K344K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr12:52200795 C>A maps to NM_014191.2 I1842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr12:52200795 C>A maps to NM_014191.2 I1842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr12:55863388 G>A maps to NM_001005499.1 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr12:55863388 G>A maps to NM_001005499.1 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr12:69656337 A>G maps to ENST00000266679 *589W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr12:69656337 A>G maps to ENST00000266679 *589W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr12:125397804 G>C maps to NM_021009.5 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr12:125397804 G>C maps to NM_021009.5 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr14:39769087 A>T maps to ENST00000396158 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr14:39769087 A>T maps to ENST00000396158 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr14:61997129 C>A maps to NM_006255.3 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr14:61997129 C>A maps to NM_006255.3 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr15:33955092 G>T maps to NM_001036.3 E1788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr15:33955092 G>T maps to NM_001036.3 E1788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr16:19718477 G>C maps to NM_001012991.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr16:19718477 G>C maps to NM_001012991.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr16:28508716 G>C maps to NM_018690.2 V776V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr16:28508716 G>C maps to NM_018690.2 V776V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr17:7557505 C>T maps to NM_001678.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr17:7557505 C>T maps to NM_001678.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr17:79410354 C>T maps to ENST00000436173 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr17:79410354 C>T maps to ENST00000436173 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr19:8131096 C>T maps to NM_032447.3 L2712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr19:8131096 C>T maps to NM_032447.3 L2712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr19:8188396 G>A maps to NM_032447.3 C1011C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr19:8188396 G>A maps to NM_032447.3 C1011C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr19:10753953 G>A did not map to a codon.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr19:10753953 G>A did not map to a codon.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr19:14513675 T>C did not map to a codon.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr19:14513675 T>C did not map to a codon.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr19:18084990 G>C maps to ENST00000222249 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr19:18084990 G>C maps to ENST00000222249 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr19:18191666 C>T maps to NM_005535.1 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr19:18191666 C>T maps to NM_005535.1 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr2:33412050 C>T maps to ENST00000354476 Q444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr2:33412050 C>T maps to ENST00000354476 Q444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr2:179528603 G>A maps to ENST00000392423 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr2:179528603 G>A maps to ENST00000392423 I404I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr20:3202540 C>T maps to NM_033453.2 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr20:3202540 C>T maps to NM_033453.2 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr20:33764085 G>A maps to NM_006404.3 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr20:33764085 G>A maps to NM_006404.3 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr20:46301110 C>A maps to NM_001161841.1 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr20:46301110 C>A maps to NM_001161841.1 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr22:19950330 C>T maps to NM_001135162.1 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr22:19950330 C>T maps to NM_001135162.1 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr3:50313226 G>A maps to NM_004636.2 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr3:50313226 G>A maps to NM_004636.2 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr3:157815816 C>T maps to NM_003030.4 *356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr3:157815816 C>T maps to NM_003030.4 *356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr4:187627773 G>A maps to ENST00000260147 R1070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr4:187627773 G>A maps to ENST00000260147 R1070*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr5:13719087 A>G maps to NM_001369.2 A4134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr5:13719087 A>G maps to NM_001369.2 A4134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr5:14387623 G>A maps to NM_007118.2 E1216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr5:14387623 G>A maps to NM_007118.2 E1216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr5:64521915 G>T maps to NM_197941.2 C688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr5:64521915 G>T maps to NM_197941.2 C688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr5:74696050 C>G maps to NM_001130105.1 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr5:74696050 C>G maps to NM_001130105.1 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr5:140263364 G>A maps to NM_018904.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr5:140263364 G>A maps to NM_018904.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr6:32975991 G>A maps to NM_002119.3 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr6:32975991 G>A maps to NM_002119.3 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr6:53373485 G>T maps to NM_001498.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr6:53373485 G>T maps to NM_001498.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr7:12263953 A>G maps to NM_018374.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr7:12263953 A>G maps to NM_018374.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr8:77767247 G>A maps to NM_024721.4 R2697R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr8:77767247 G>A maps to NM_024721.4 R2697R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr8:90926440 G>A maps to NM_001126111.1 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr8:90926440 G>A maps to NM_001126111.1 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr8:113267645 A>T maps to NM_198123.1 C3291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr8:113267645 A>T maps to NM_198123.1 C3291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chrX:1508617 G>C maps to NM_001636.3 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chrX:1508617 G>C maps to NM_001636.3 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chrX:12735806 G>A maps to ENST00000429478 P944P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chrX:12735806 G>A maps to ENST00000429478 P944P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chrX:23724803 G>A maps to NM_001037171.1 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chrX:23724803 G>A maps to NM_001037171.1 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chrX:54955856 T>G maps to NM_001039705.1 G900G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chrX:54955856 T>G maps to NM_001039705.1 G900G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr16:2762621 C>G maps to NM_031948.3 *291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7091-01A-11D-2012-08 chr16:2762621 C>G maps to NM_031948.3 *291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:2160912 C>T maps to NM_003036.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:2160912 C>T maps to NM_003036.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:27332875 G>A maps to NM_052943.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:27332875 G>A maps to NM_052943.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:36031041 C>T maps to NM_001014839.1 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:36031041 C>T maps to NM_001014839.1 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:59812063 G>C maps to NM_001113411.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:59812063 G>C maps to NM_001113411.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:120057079 C>T maps to ENST00000235547 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:120057079 C>T maps to ENST00000235547 R314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:150900252 G>A maps to NM_001145415.1 E21E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:150900252 G>A maps to NM_001145415.1 E21E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:180471272 G>A maps to NM_032360.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:180471272 G>A maps to NM_032360.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:205039106 C>A maps to NM_005076.3 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:205039106 C>A maps to NM_005076.3 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:213277817 C>A maps to NM_012424.3 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:213277817 C>A maps to NM_012424.3 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:233394515 G>A maps to NM_014801.3 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:233394515 G>A maps to NM_014801.3 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:234745080 C>A maps to NM_182972.2 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:234745080 C>A maps to NM_182972.2 E54*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CV-7095-01A-21D-2012-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-CV-7095-01A-21D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr10:27423859 G>A maps to NM_139312.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr10:27423859 G>A maps to NM_139312.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr10:95791018 T>C maps to ENST00000371380 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr10:95791018 T>C maps to ENST00000371380 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr11:36472864 C>G maps to NM_001160167.1 S231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr11:36472864 C>G maps to NM_001160167.1 S231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr11:45926321 C>G maps to NM_005456.2 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr11:45926321 C>G maps to NM_005456.2 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr11:64005047 A>C maps to NM_003377.3 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr11:64005047 A>C maps to NM_003377.3 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr11:67077771 G>T maps to NM_017857.3 E549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr11:67077771 G>T maps to NM_017857.3 E549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr12:11183043 C>G maps to NM_176885.2 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr12:11183043 C>G maps to NM_176885.2 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr12:48477536 G>C maps to ENST00000004980 S130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr12:48477536 G>C maps to ENST00000004980 S130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr12:57538854 G>A maps to NM_002332.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr12:57538854 G>A maps to NM_002332.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr12:66990675 C>T maps to ENST00000359742 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr12:66990675 C>T maps to ENST00000359742 Q29Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr12:117013806 C>G maps to NM_001085481.1 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr12:117013806 C>G maps to NM_001085481.1 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr13:103338494 G>A maps to NM_001010977.1 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr13:103338494 G>A maps to NM_001010977.1 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr14:51224284 G>A maps to NM_020921.3 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr14:51224284 G>A maps to NM_020921.3 L1155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr14:60976680 A>T maps to ENST00000381716 K248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr14:60976680 A>T maps to ENST00000381716 K248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr15:50791261 C>T maps to NM_005154.3 R1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr15:50791261 C>T maps to NM_005154.3 R1112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr15:56207862 G>A maps to ENST00000508342 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr15:56207862 G>A maps to ENST00000508342 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr15:74559049 G>A maps to ENST00000321288 K320K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr15:74559049 G>A maps to ENST00000321288 K320K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr15:76467993 G>A maps to NM_152335.2 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr15:76467993 G>A maps to NM_152335.2 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr16:3777766 G>A maps to NM_004380.2 V2427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr16:3777766 G>A maps to NM_004380.2 V2427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr16:51174818 C>T maps to ENST00000251020 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr16:51174818 C>T maps to ENST00000251020 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr16:66766352 G>C maps to NM_006141.2 S273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr16:66766352 G>C maps to NM_006141.2 S273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr16:68344296 A>G maps to NM_032178.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr16:68344296 A>G maps to NM_032178.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr17:6373603 G>A maps to NM_031220.3 D583D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr17:6373603 G>A maps to NM_031220.3 D583D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr17:7696465 C>T maps to NM_020877.2 L2504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr17:7696465 C>T maps to NM_020877.2 L2504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr17:8021161 C>T maps to ENST00000380149 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr17:8021161 C>T maps to ENST00000380149 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr17:10547748 G>A maps to NM_002470.2 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr17:10547748 G>A maps to NM_002470.2 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr17:12642623 A>T maps to NM_001146312.1 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr17:12642623 A>T maps to NM_001146312.1 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr17:76991154 C>T maps to NM_138793.3 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr17:76991154 C>T maps to NM_138793.3 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr18:55143900 C>T maps to NM_004852.2 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr18:55143900 C>T maps to NM_004852.2 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:14070283 G>A maps to NM_138353.2 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:14070283 G>A maps to NM_138353.2 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:33870421 A>T maps to NM_001806.2 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:33870421 A>T maps to NM_001806.2 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:49636570 G>A maps to NM_003660.2 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:49636570 G>A maps to NM_003660.2 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:50925755 G>A maps to NM_003121.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:50925755 G>A maps to NM_003121.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:51994963 C>T maps to NM_053003.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:51994963 C>T maps to NM_053003.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:52497521 G>A maps to ENST00000354939 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:52497521 G>A maps to ENST00000354939 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:53612313 G>T maps to NM_001164309.1 Y328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:53612313 G>T maps to NM_001164309.1 Y328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:53912280 G>A maps to NM_001040185.1 Q491Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr19:53912280 G>A maps to NM_001040185.1 Q491Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr2:27601469 C>T maps to NM_144631.4 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr2:27601469 C>T maps to NM_144631.4 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr2:32724765 C>G maps to NM_016252.3 S2874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr2:32724765 C>G maps to NM_016252.3 S2874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr2:100916182 C>T maps to NM_198461.3 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr2:100916182 C>T maps to NM_198461.3 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr2:118758499 G>C maps to NM_019044.4 S87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr2:118758499 G>C maps to NM_019044.4 S87*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CV-7095-01A-21D-2012-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CV-7095-01A-21D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr2:217124225 C>A maps to NM_020814.2 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr2:217124225 C>A maps to NM_020814.2 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr20:31590694 C>T maps to NM_080675.3 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr20:31590694 C>T maps to NM_080675.3 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr20:31606866 G>A did not map to a codon.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr20:31606866 G>A did not map to a codon.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr21:46957702 C>T maps to NM_194255.1 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr21:46957702 C>T maps to NM_194255.1 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr21:47697543 G>A maps to NM_003906.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr21:47697543 G>A maps to NM_003906.3 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr22:41573027 C>A maps to NM_001429.3 C1771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr22:41573027 C>A maps to NM_001429.3 C1771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr3:45804559 C>G maps to NM_020208.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr3:45804559 C>G maps to NM_020208.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr3:170802910 G>A maps to NM_015028.2 A998A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr3:170802910 G>A maps to NM_015028.2 A998A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr4:959303 G>A maps to NM_001347.2 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr4:959303 G>A maps to NM_001347.2 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr4:77675520 C>T maps to NM_020859.3 L1295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr4:77675520 C>T maps to NM_020859.3 L1295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr4:79403006 C>T maps to NM_025074.6 F2831F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr4:79403006 C>T maps to NM_025074.6 F2831F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr4:187539251 G>A maps to ENST00000260147 Q2833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr4:187539251 G>A maps to ENST00000260147 Q2833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr5:36265594 G>C maps to NM_001161429.1 S124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr5:36265594 G>C maps to NM_001161429.1 S124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr5:140476459 T>C maps to NM_018936.2 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr5:140476459 T>C maps to NM_018936.2 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr5:140482312 T>C maps to NM_018937.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr5:140482312 T>C maps to NM_018937.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr5:140568970 T>C maps to NM_019119.3 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr5:140568970 T>C maps to NM_019119.3 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr5:140595774 T>C maps to NM_018933.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr5:140595774 T>C maps to NM_018933.2 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr5:180047254 C>A maps to NM_182925.4 G820G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr5:180047254 C>A maps to NM_182925.4 G820G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr6:29796371 C>T maps to ENST00000376828 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr6:29796371 C>T maps to ENST00000376828 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr6:30154333 C>T maps to NM_003449.3 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr6:30154333 C>T maps to NM_003449.3 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr6:37411844 C>T maps to NM_015050.2 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr6:37411844 C>T maps to NM_015050.2 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr6:43214424 G>A maps to NM_032538.1 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr6:43214424 G>A maps to NM_032538.1 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr6:134210543 C>T maps to NM_003206.3 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr6:134210543 C>T maps to NM_003206.3 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr7:82579178 T>A maps to NM_033026.5 T3575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr7:82579178 T>A maps to NM_033026.5 T3575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr7:97832935 G>A maps to NM_014916.3 P1386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr7:97832935 G>A maps to NM_014916.3 P1386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr7:139796487 G>A maps to NM_030647.1 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr7:139796487 G>A maps to NM_030647.1 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr7:148288040 C>G maps to NM_145304.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr7:148288040 C>G maps to NM_145304.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr8:121290785 G>C maps to NM_021110.1 V1150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr8:121290785 G>C maps to NM_021110.1 V1150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr8:144998291 C>T maps to NM_201380.2 E2072E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr8:144998291 C>T maps to NM_201380.2 E2072E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr9:35385811 T>C did not map to a codon.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr9:35385811 T>C did not map to a codon.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr9:35403455 C>T maps to ENST00000396787 L1481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr9:35403455 C>T maps to ENST00000396787 L1481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr9:79910534 T>G maps to ENST00000376646 T1195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr9:79910534 T>G maps to ENST00000376646 T1195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr9:116823770 G>A maps to NM_001633.3 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr9:116823770 G>A maps to NM_001633.3 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr9:117266937 C>T maps to NM_015404.3 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr9:117266937 C>T maps to NM_015404.3 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr9:125861041 A>T maps to NM_012197.3 K928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr9:125861041 A>T maps to NM_012197.3 K928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr9:135984210 C>T maps to NM_006266.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr9:135984210 C>T maps to NM_006266.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chrX:31986548 G>C maps to ENST00000357033 S2174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chrX:31986548 G>C maps to ENST00000357033 S2174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chrX:48542319 C>G maps to NM_000377.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chrX:48542319 C>G maps to NM_000377.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chrX:140995472 G>A maps to NM_005462.4 E761E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chrX:140995472 G>A maps to NM_005462.4 E761E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:110590407 G>A maps to NM_033088.2 K526K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr1:110590407 G>A maps to NM_033088.2 K526K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr14:23887504 A>C maps to NM_000257.2 L1361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7095-01A-21D-2012-08 chr14:23887504 A>C maps to NM_000257.2 L1361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr1:21013937 G>A maps to NM_020816.2 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr1:21013937 G>A maps to NM_020816.2 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr1:152279920 A>G maps to NM_002016.1 L2481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr1:152279920 A>G maps to NM_002016.1 L2481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr1:156874632 C>T maps to NM_001080471.1 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr1:156874632 C>T maps to NM_001080471.1 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr1:211534066 T>C maps to ENST00000427925 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr1:211534066 T>C maps to ENST00000427925 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr11:118107897 T>C maps to NM_198275.1 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr11:118107897 T>C maps to NM_198275.1 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr12:43777689 G>A maps to ENST00000389420 Q1515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr12:43777689 G>A maps to ENST00000389420 Q1515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr14:74327273 C>T maps to NM_152444.2 R24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr14:74327273 C>T maps to NM_152444.2 R24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr14:102874943 G>C maps to NM_014844.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr14:102874943 G>C maps to NM_014844.3 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr16:11016080 G>A maps to NM_000246.3 P1069P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr16:11016080 G>A maps to NM_000246.3 P1069P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr16:80718468 G>A maps to NM_152342.2 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr16:80718468 G>A maps to NM_152342.2 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr17:10440763 G>C maps to NM_017534.5 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr17:10440763 G>C maps to NM_017534.5 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr17:59115268 A>G maps to ENST00000407086 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr17:59115268 A>G maps to ENST00000407086 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr17:72341018 C>T maps to NM_153209.3 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr17:72341018 C>T maps to NM_153209.3 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr18:48603079 C>T maps to NM_005359.5 Q461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr18:48603079 C>T maps to NM_005359.5 Q461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr19:17436102 G>A maps to NM_020959.2 A918A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr19:17436102 G>A maps to NM_020959.2 A918A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr19:44610696 T>A maps to NM_013398.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr19:44610696 T>A maps to NM_013398.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr2:239988449 C>A maps to NM_006037.3 E986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr2:239988449 C>A maps to NM_006037.3 E986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr20:43945403 C>A maps to NM_014276.2 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr20:43945403 C>A maps to NM_014276.2 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr20:61598791 C>A maps to NM_022082.3 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr20:61598791 C>A maps to NM_022082.3 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr3:112198457 C>A maps to NM_181780.3 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr3:112198457 C>A maps to NM_181780.3 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr3:129324753 C>T maps to NM_015103.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr3:129324753 C>T maps to NM_015103.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr3:131254047 T>C maps to ENST00000502818 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr3:131254047 T>C maps to ENST00000502818 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr4:129776937 C>T maps to NM_199320.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr4:129776937 C>T maps to NM_199320.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr4:140265371 T>C maps to NM_057175.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr4:140265371 T>C maps to NM_057175.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr4:146435851 G>A maps to NM_001003688.1 W29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr4:146435851 G>A maps to NM_001003688.1 W29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr4:175162339 G>T maps to NM_012180.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr4:175162339 G>T maps to NM_012180.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr5:169810823 C>A maps to NM_004137.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr5:169810823 C>A maps to NM_004137.2 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr6:32917063 C>T maps to NM_006120.3 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr6:32917063 C>T maps to NM_006120.3 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr6:43305057 A>G maps to NM_014345.2 D2226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr6:43305057 A>G maps to NM_014345.2 D2226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr7:100677783 T>C maps to NM_001040105.1 G1029G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr7:100677783 T>C maps to NM_001040105.1 G1029G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr9:990053 A>G maps to NM_021240.2 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr9:990053 A>G maps to NM_021240.2 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr9:21367982 C>T maps to NM_006900.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr9:21367982 C>T maps to NM_006900.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr9:123904512 A>C maps to NM_007018.4 R946R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr9:123904512 A>C maps to NM_007018.4 R946R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr9:131233666 C>T maps to NM_153435.1 H231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr9:131233666 C>T maps to NM_153435.1 H231H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chrX:151935539 G>A maps to NM_005362.3 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chrX:151935539 G>A maps to NM_005362.3 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr9:139879315 C>T maps to NM_207510.3 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr9:139879315 C>T maps to NM_207510.3 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:14108592 C>T maps to NM_012231.4 Q1435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:14108592 C>T maps to NM_012231.4 Q1435*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:19505573 G>A maps to ENST00000375267 D775D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:19505573 G>A maps to ENST00000375267 D775D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:32134423 C>T maps to NM_001856.3 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:32134423 C>T maps to NM_001856.3 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:89521737 C>T maps to NM_002053.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:89521737 C>T maps to NM_002053.2 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:115153709 G>C maps to ENST00000393274 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:115153709 G>C maps to ENST00000393274 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:152282918 T>C maps to NM_002016.1 A1481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:152282918 T>C maps to NM_002016.1 A1481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:160156137 C>T maps to NM_144699.3 L1014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:160156137 C>T maps to NM_144699.3 L1014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:180012228 C>T maps to NM_014810.4 V1467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:180012228 C>T maps to NM_014810.4 V1467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:208257733 C>T maps to NM_025179.3 Q763Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:208257733 C>T maps to NM_025179.3 Q763Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:248813996 G>A maps to NM_001001824.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr1:248813996 G>A maps to NM_001001824.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr10:60936717 C>T maps to NM_032439.3 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr10:60936717 C>T maps to NM_032439.3 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr10:88277757 G>C maps to ENST00000342368 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr10:88277757 G>C maps to ENST00000342368 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr10:98714868 G>A maps to NM_001170765.1 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr10:98714868 G>A maps to NM_001170765.1 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr10:135015068 G>A maps to ENST00000368572 S1020S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr10:135015068 G>A maps to ENST00000368572 S1020S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr10:135015188 C>T maps to ENST00000368572 G1060G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr10:135015188 C>T maps to ENST00000368572 G1060G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:721617 G>A maps to NM_022772.3 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:721617 G>A maps to NM_022772.3 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:7334937 A>G maps to NM_175733.3 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:7334937 A>G maps to NM_175733.3 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:8724163 G>C maps to NM_005418.3 S892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:8724163 G>C maps to NM_005418.3 S892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:55418943 G>T maps to NM_001004059.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:55418943 G>T maps to NM_001004059.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:59377943 G>A maps to NM_002556.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:59377943 G>A maps to NM_002556.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:67223245 C>T maps to NM_145200.3 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:67223245 C>T maps to NM_145200.3 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:75277819 C>T maps to NM_001235.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:75277819 C>T maps to NM_001235.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:77775067 C>G maps to NM_003251.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr11:77775067 C>G maps to NM_003251.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr12:11091368 T>C maps to NM_023922.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr12:11091368 T>C maps to NM_023922.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr12:56477580 G>A maps to NM_001982.2 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr12:56477580 G>A maps to NM_001982.2 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr12:85434272 A>G maps to NM_001079910.1 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr12:85434272 A>G maps to NM_001079910.1 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr12:104063326 G>A maps to NM_017564.9 K727K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr12:104063326 G>A maps to NM_017564.9 K727K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr12:104461750 G>C maps to NM_013320.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr12:104461750 G>C maps to NM_013320.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr12:123102941 C>G maps to NM_014708.4 S2028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr12:123102941 C>G maps to NM_014708.4 S2028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr13:111996451 C>T maps to NM_152324.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr13:111996451 C>T maps to NM_152324.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr13:112722211 G>A maps to NM_005986.2 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr13:112722211 G>A maps to NM_005986.2 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr14:93199104 G>A maps to NM_005606.6 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr14:93199104 G>A maps to NM_005606.6 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr14:94083610 G>A maps to ENST00000393153 R1417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr14:94083610 G>A maps to ENST00000393153 R1417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr15:41804948 C>T maps to NM_002344.5 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr15:41804948 C>T maps to NM_002344.5 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr15:65319318 G>C maps to NM_139242.3 S90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr15:65319318 G>C maps to NM_139242.3 S90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr16:1143808 G>A maps to NM_207419.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr16:1143808 G>A maps to NM_207419.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr16:3639183 C>T maps to NM_032444.2 Q1485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr16:3639183 C>T maps to NM_032444.2 Q1485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr16:14015907 G>A maps to NM_005236.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr16:14015907 G>A maps to NM_005236.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr16:15661908 C>T maps to NM_033201.2 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr16:15661908 C>T maps to NM_033201.2 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr16:70515273 G>C maps to NM_015386.2 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr16:70515273 G>C maps to NM_015386.2 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr16:75665699 C>T maps to NM_001130089.1 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr16:75665699 C>T maps to NM_001130089.1 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr17:1582625 C>G maps to NM_006445.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr17:1582625 C>G maps to NM_006445.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr17:8422109 C>G did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr17:8422109 C>G did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr17:10442662 G>A maps to NM_017534.5 N425N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr17:10442662 G>A maps to NM_017534.5 N425N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr17:45924943 G>A maps to NM_199262.2 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr17:45924943 G>A maps to NM_199262.2 F284F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CV-7099-01A-41D-2012-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CV-7099-01A-41D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr18:54483273 C>G maps to NM_015285.2 S1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr18:54483273 C>G maps to NM_015285.2 S1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:3179317 G>A maps to NM_003775.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:3179317 G>A maps to NM_003775.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:6684803 T>C maps to NM_000064.2 K1337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:6684803 T>C maps to NM_000064.2 K1337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:15291044 A>G maps to NM_000435.2 C1055C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:15291044 A>G maps to NM_000435.2 C1055C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:17615339 C>T maps to NM_198580.1 F620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:17615339 C>T maps to NM_198580.1 F620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:36853090 C>T maps to NM_020917.2 W20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:36853090 C>T maps to NM_020917.2 W20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:38103197 C>T maps to NM_152606.3 C339C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:38103197 C>T maps to NM_152606.3 C339C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:45910388 G>A maps to ENST00000423698 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:45910388 G>A maps to ENST00000423698 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:53612342 G>A maps to NM_001164309.1 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:53612342 G>A maps to NM_001164309.1 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:58928445 C>T maps to NM_173548.1 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:58928445 C>T maps to NM_173548.1 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:58967528 C>T maps to NM_207395.2 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr19:58967528 C>T maps to NM_207395.2 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:26204429 G>C maps to NM_002254.6 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:26204429 G>C maps to NM_002254.6 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:32667174 G>A maps to NM_016252.3 E1329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:32667174 G>A maps to NM_016252.3 E1329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:54856683 G>T maps to NM_003128.2 E805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:54856683 G>T maps to NM_003128.2 E805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:68882428 C>T maps to NM_138964.2 Y301Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:68882428 C>T maps to NM_138964.2 Y301Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:113780313 G>A maps to NM_014438.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:113780313 G>A maps to NM_014438.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:113940968 C>T maps to NM_012455.2 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:113940968 C>T maps to NM_012455.2 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:120194889 C>G maps to NM_183240.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:120194889 C>G maps to NM_183240.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:200137184 G>A maps to NM_001172509.1 Q651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:200137184 G>A maps to NM_001172509.1 Q651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:202151269 C>T maps to NM_001080125.1 Q524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr2:202151269 C>T maps to NM_001080125.1 Q524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr20:20453516 G>A maps to NM_020343.3 N1817N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr20:20453516 G>A maps to NM_020343.3 N1817N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr20:25011401 G>A maps to NM_032501.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr20:25011401 G>A maps to NM_032501.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr20:61527744 C>G did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr20:61527744 C>G did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr21:32253854 G>T did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr21:32253854 G>T did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr21:46057495 G>A maps to NM_181688.1 Q54Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr21:46057495 G>A maps to NM_181688.1 Q54Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr22:25755870 G>C maps to NM_001135772.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr22:25755870 G>C maps to NM_001135772.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr22:44583757 C>T maps to NM_001137606.1 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr22:44583757 C>T maps to NM_001137606.1 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr3:2777986 C>G maps to NM_175607.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr3:2777986 C>G maps to NM_175607.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr3:125872404 G>C maps to ENST00000273450 S257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr3:125872404 G>C maps to ENST00000273450 S257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr3:127294642 G>A maps to NM_001136053.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr3:127294642 G>A maps to NM_001136053.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr3:136667113 C>G maps to NM_006153.4 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr3:136667113 C>G maps to NM_006153.4 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr3:149589831 C>G maps to NM_007282.4 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr3:149589831 C>G maps to NM_007282.4 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr3:150840607 G>A maps to NM_053002.4 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr3:150840607 G>A maps to NM_053002.4 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr3:168833802 G>A maps to NM_004991.3 F619F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr3:168833802 G>A maps to NM_004991.3 F619F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr4:158284165 C>T maps to NM_000826.3 N874N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr4:158284165 C>T maps to NM_000826.3 N874N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr4:166184407 A>G maps to NM_001161521.1 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr4:166184407 A>G maps to NM_001161521.1 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr4:187525000 G>C maps to ENST00000260147 S3563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr4:187525000 G>C maps to ENST00000260147 S3563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:1409144 G>A maps to NM_001044.4 F498F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:1409144 G>A maps to NM_001044.4 F498F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:14387878 C>T maps to NM_007118.2 I1268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:14387878 C>T maps to NM_007118.2 I1268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:61747670 C>T maps to NM_001134779.1 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:61747670 C>T maps to NM_001134779.1 R183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:96248383 C>T maps to NM_001130140.1 Q800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:96248383 C>T maps to NM_001130140.1 Q800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:121309962 C>T maps to NM_152546.2 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:121309962 C>T maps to NM_152546.2 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:157218824 G>A maps to NM_001195555.1 D422D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:157218824 G>A maps to NM_001195555.1 D422D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:171534827 C>G maps to NM_005990.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:171534827 C>G maps to NM_005990.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:176523643 C>T maps to NM_213647.1 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr5:176523643 C>T maps to NM_213647.1 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:7586032 G>A maps to NM_004415.2 R2846R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:7586032 G>A maps to NM_004415.2 R2846R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:26043801 C>T maps to NM_021062.2 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:26043801 C>T maps to NM_021062.2 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:27839925 C>T maps to NM_003533.2 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:27839925 C>T maps to NM_003533.2 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:29910683 G>A maps to ENST00000376806 W75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:29910683 G>A maps to ENST00000376806 W75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:34498109 C>T maps to NM_020804.3 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:34498109 C>T maps to NM_020804.3 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:71442123 C>T maps to NM_001044305.1 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:71442123 C>T maps to NM_001044305.1 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:110423088 C>T maps to NM_003931.2 E408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:110423088 C>T maps to NM_003931.2 E408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:137815022 C>T maps to NM_175747.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:137815022 C>T maps to NM_175747.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:150210517 G>A maps to NM_139165.1 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:150210517 G>A maps to NM_139165.1 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:150210685 G>A maps to NM_139165.1 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr6:150210685 G>A maps to NM_139165.1 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr7:50467664 G>A maps to NM_006060.3 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr7:50467664 G>A maps to NM_006060.3 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr7:87179525 G>C maps to NM_000927.3 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr7:87179525 G>C maps to NM_000927.3 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr7:100253068 G>A maps to NM_016188.4 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr7:100253068 G>A maps to NM_016188.4 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr7:148427270 G>A maps to NM_003592.2 Q19Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr7:148427270 G>A maps to NM_003592.2 Q19Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr7:151262821 A>T maps to NM_016203.3 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr7:151262821 A>T maps to NM_016203.3 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr8:37696478 G>C maps to NM_032777.9 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr8:37696478 G>C maps to NM_032777.9 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr8:66992625 C>T maps to NM_033105.4 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr8:66992625 C>T maps to NM_033105.4 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr8:91940499 G>A maps to NM_022351.4 Q222Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr8:91940499 G>A maps to NM_022351.4 Q222Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr8:98943557 C>T maps to ENST00000254898 Q174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr8:98943557 C>T maps to ENST00000254898 Q174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr8:133898882 C>G maps to NM_003235.4 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr8:133898882 C>G maps to NM_003235.4 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr8:144990623 C>T maps to NM_201380.2 V4592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr8:144990623 C>T maps to NM_201380.2 V4592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr9:34635730 G>T maps to NM_005866.2 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr9:34635730 G>T maps to NM_005866.2 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr9:37740339 G>C maps to NM_014907.2 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr9:37740339 G>C maps to NM_014907.2 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr9:134165520 C>G maps to NM_032728.3 S46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr9:134165520 C>G maps to NM_032728.3 S46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr9:136031309 G>A maps to NM_021996.4 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr9:136031309 G>A maps to NM_021996.4 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr9:140109352 C>T maps to NM_001144026.1 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr9:140109352 C>T maps to NM_001144026.1 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr9:140728823 C>T maps to NM_024757.4 D1188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr9:140728823 C>T maps to NM_024757.4 D1188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chrX:49067780 C>A did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chrX:49067780 C>A did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chrX:49958649 C>T maps to NM_003886.2 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chrX:49958649 C>T maps to NM_003886.2 E238E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chrX:118763372 G>A maps to ENST00000394612 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chrX:118763372 G>A maps to ENST00000394612 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chrX:134989481 C>T maps to NM_018666.2 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chrX:134989481 C>T maps to NM_018666.2 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chrX:134991056 G>A maps to NM_018666.2 K492K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chrX:134991056 G>A maps to NM_018666.2 K492K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chrX:152845455 C>T maps to NM_001001344.2 F1121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chrX:152845455 C>T maps to NM_001001344.2 F1121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7100-01A-11D-2012-08 chr1:19451142 T>G maps to ENST00000375267 L3160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7100-01A-11D-2012-08 chr1:19451142 T>G maps to ENST00000375267 L3160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7100-01A-11D-2012-08 chr20:8678322 C>T maps to NM_015192.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7100-01A-11D-2012-08 chr20:8678322 C>T maps to NM_015192.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7100-01A-11D-2012-08 chr3:160239584 G>A maps to NM_002268.3 H295H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7100-01A-11D-2012-08 chr3:160239584 G>A maps to NM_002268.3 H295H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7100-01A-11D-2012-08 chrX:10201602 C>T maps to NM_001830.3 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7100-01A-11D-2012-08 chrX:10201602 C>T maps to NM_001830.3 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr1:52498548 C>A maps to NM_138417.2 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr1:52498548 C>A maps to NM_138417.2 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr1:155629471 T>A maps to ENST00000368339 T881T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr1:155629471 T>A maps to ENST00000368339 T881T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr1:186158871 G>A maps to NM_031935.2 V5590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr1:186158871 G>A maps to NM_031935.2 V5590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr1:236911017 T>C maps to NM_001103.2 I486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr1:236911017 T>C maps to NM_001103.2 I486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr1:237813232 C>T maps to NM_001035.2 A2523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr1:237813232 C>T maps to NM_001035.2 A2523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr1:246810609 C>T maps to NM_152609.2 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr1:246810609 C>T maps to NM_152609.2 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr1:247614633 G>A maps to NM_001004492.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr1:247614633 G>A maps to NM_001004492.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr10:31810428 A>G maps to NM_001174096.1 T723T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr10:31810428 A>G maps to NM_001174096.1 T723T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr10:54074845 G>T did not map to a codon.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr10:54074845 G>T did not map to a codon.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr11:10064471 A>G maps to NM_030962.3 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr11:10064471 A>G maps to NM_030962.3 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr11:17741385 T>G maps to NM_002478.4 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr11:17741385 T>G maps to NM_002478.4 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr12:81661804 T>C maps to NM_003625.2 E1124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr12:81661804 T>C maps to NM_003625.2 E1124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr14:21499311 C>A maps to NM_173846.4 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr14:21499311 C>A maps to NM_173846.4 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr14:23243253 A>G maps to NM_001126106.1 D439D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr14:23243253 A>G maps to NM_001126106.1 D439D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr14:105920570 G>A maps to NM_004689.3 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr14:105920570 G>A maps to NM_004689.3 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr15:83478537 C>T maps to NM_001080435.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr15:83478537 C>T maps to NM_001080435.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr15:85487996 C>T maps to NM_004213.3 Y591Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr15:85487996 C>T maps to NM_004213.3 Y591Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr16:19586418 G>A did not map to a codon.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr16:19586418 G>A did not map to a codon.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr16:22271781 G>C did not map to a codon.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr16:22271781 G>C did not map to a codon.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr16:67683450 C>T maps to NM_001013838.1 I616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr16:67683450 C>T maps to NM_001013838.1 I616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr16:67917556 G>A maps to NM_014329.3 P1312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr16:67917556 G>A maps to NM_014329.3 P1312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr16:75276925 G>T maps to NM_001170714.1 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr16:75276925 G>T maps to NM_001170714.1 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr17:19610063 G>A maps to NM_152908.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr17:19610063 G>A maps to NM_152908.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr17:39412083 C>A maps to ENST00000431129 C155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr17:39412083 C>A maps to ENST00000431129 C155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr17:46153469 G>A maps to ENST00000442683 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr17:46153469 G>A maps to ENST00000442683 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr17:80865684 G>A maps to NM_005993.4 Q657Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr17:80865684 G>A maps to NM_005993.4 Q657Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr18:5394793 T>A did not map to a codon.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr18:5394793 T>A did not map to a codon.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr18:34855108 G>T maps to NM_020180.3 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr18:34855108 G>T maps to NM_020180.3 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr18:60242730 C>T maps to NM_017742.4 S1139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr18:60242730 C>T maps to NM_017742.4 S1139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr19:8148206 G>T maps to NM_032447.3 C2379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr19:8148206 G>T maps to NM_032447.3 C2379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr19:22156524 G>A maps to NM_007153.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr19:22156524 G>A maps to NM_007153.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr19:31039642 C>A maps to NM_014717.1 V1039V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr19:31039642 C>A maps to NM_014717.1 V1039V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr19:55501498 G>T maps to NM_017852.3 E826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr19:55501498 G>T maps to NM_017852.3 E826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr20:43929778 C>T maps to ENST00000372754 E325E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr20:43929778 C>T maps to ENST00000372754 E325E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr22:18384650 G>A maps to NM_015241.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr22:18384650 G>A maps to NM_015241.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr22:19344525 G>T maps to NM_003325.3 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr22:19344525 G>T maps to NM_003325.3 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr22:32198786 A>T maps to NM_001136029.1 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr22:32198786 A>T maps to NM_001136029.1 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr3:52723169 G>A maps to NM_014366.4 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr3:52723169 G>A maps to NM_014366.4 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr3:88188517 C>T maps to NM_018293.2 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr3:88188517 C>T maps to NM_018293.2 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr3:122345842 A>G maps to NM_001113523.1 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr3:122345842 A>G maps to NM_001113523.1 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr3:171451287 T>C maps to NM_002662.3 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr3:171451287 T>C maps to NM_002662.3 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr3:182871532 G>A maps to NM_014398.3 N232N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr3:182871532 G>A maps to NM_014398.3 N232N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr4:6302535 C>T maps to NM_006005.3 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr4:6302535 C>T maps to NM_006005.3 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr4:89827586 G>C maps to NM_014883.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr4:89827586 G>C maps to NM_014883.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr5:140201941 T>G maps to NM_018908.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr5:140201941 T>G maps to NM_018908.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr5:156786086 C>A maps to ENST00000442283 I941I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr5:156786086 C>A maps to ENST00000442283 I941I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr6:25701544 G>T maps to NM_006998.3 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr6:25701544 G>T maps to NM_006998.3 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr6:56917578 C>T maps to NM_020931.2 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr6:56917578 C>T maps to NM_020931.2 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr6:63990177 G>A maps to NM_016571.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr6:63990177 G>A maps to NM_016571.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr7:23809340 C>A maps to NM_031414.3 S560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr7:23809340 C>A maps to NM_031414.3 S560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr7:43590144 C>T maps to NM_015052.3 R1450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr7:43590144 C>T maps to NM_015052.3 R1450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr7:91691799 C>T maps to NM_005751.4 Q1993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr7:91691799 C>T maps to NM_005751.4 Q1993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr7:94054508 C>T maps to NM_000089.3 N918N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr7:94054508 C>T maps to NM_000089.3 N918N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr7:99128781 C>G maps to NM_014569.3 S477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr7:99128781 C>G maps to NM_014569.3 S477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr7:154561125 G>C did not map to a codon.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr7:154561125 G>C did not map to a codon.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr8:1719414 C>T maps to NM_018941.3 D65D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr8:1719414 C>T maps to NM_018941.3 D65D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr8:4494991 G>A maps to NM_033225.5 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr8:4494991 G>A maps to NM_033225.5 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr8:38005822 G>C maps to NM_000349.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr8:38005822 G>C maps to NM_000349.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr8:38066592 A>G maps to NM_004874.2 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr8:38066592 A>G maps to NM_004874.2 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr8:64099526 C>T maps to ENST00000339066 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr8:64099526 C>T maps to ENST00000339066 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr8:113585855 G>A maps to NM_198123.1 L1306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr8:113585855 G>A maps to NM_198123.1 L1306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr9:21971027 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr9:21971027 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr9:119495732 C>T maps to ENST00000313400 E822E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr9:119495732 C>T maps to ENST00000313400 E822E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr9:134073596 G>T maps to ENST00000451030 T1573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chr9:134073596 G>T maps to ENST00000451030 T1573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chrX:3021855 C>T maps to NM_004042.3 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chrX:3021855 C>T maps to NM_004042.3 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chrX:152483001 A>T maps to NM_004988.4 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7101-01A-11D-2012-08 chrX:152483001 A>T maps to NM_004988.4 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr1:158817522 C>T maps to NM_002432.1 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr1:158817522 C>T maps to NM_002432.1 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr10:16911692 G>A maps to NM_001081.3 F3132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr10:16911692 G>A maps to NM_001081.3 F3132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr11:64508538 G>A maps to ENST00000320253 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr11:64508538 G>A maps to ENST00000320253 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr11:64606236 T>C maps to NM_017525.2 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr11:64606236 T>C maps to NM_017525.2 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr11:76813989 C>T maps to NM_006189.1 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr11:76813989 C>T maps to NM_006189.1 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr12:21032550 C>T maps to NM_019844.2 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr12:21032550 C>T maps to NM_019844.2 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr12:41421671 T>A maps to NM_001843.2 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr12:41421671 T>A maps to NM_001843.2 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr12:54115807 C>T did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr12:54115807 C>T did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr12:120172976 G>A maps to ENST00000392521 T1048T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr12:120172976 G>A maps to ENST00000392521 T1048T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr14:52481132 G>T maps to NM_007361.3 R1098R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr14:52481132 G>T maps to NM_007361.3 R1098R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr14:59791159 C>G maps to NM_014992.1 S326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr14:59791159 C>G maps to NM_014992.1 S326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr14:73408451 G>C did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr14:73408451 G>C did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr16:2218132 C>T maps to NM_032271.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr16:2218132 C>T maps to NM_032271.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr16:87365040 G>A maps to NM_024735.3 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr16:87365040 G>A maps to NM_024735.3 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr18:47107899 C>T maps to NM_006033.2 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr18:47107899 C>T maps to NM_006033.2 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr18:54358526 C>G maps to NM_015285.2 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr18:54358526 C>G maps to NM_015285.2 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr19:3452480 G>T maps to ENST00000269778 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr19:3452480 G>T maps to ENST00000269778 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr19:3586840 G>A maps to NM_133261.2 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr19:3586840 G>A maps to NM_133261.2 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr19:4552582 C>T maps to NM_032108.3 K280K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr19:4552582 C>T maps to NM_032108.3 K280K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr19:19790799 A>T maps to NM_033204.2 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr19:19790799 A>T maps to NM_033204.2 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr19:58438231 G>T maps to NM_133460.1 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr19:58438231 G>T maps to NM_133460.1 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr2:122038714 C>T maps to NM_014553.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr2:122038714 C>T maps to NM_014553.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr2:220286274 G>T maps to NM_001927.3 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr2:220286274 G>T maps to NM_001927.3 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr21:45709684 C>T maps to NM_000383.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr21:45709684 C>T maps to NM_000383.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr22:20800822 C>T maps to NM_032775.3 R482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr22:20800822 C>T maps to NM_032775.3 R482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr22:41969736 C>T maps to NM_014460.3 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr22:41969736 C>T maps to NM_014460.3 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr3:127395885 C>T maps to NM_172027.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr3:127395885 C>T maps to NM_172027.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr3:139173604 C>T maps to NM_004164.2 W107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr3:139173604 C>T maps to NM_004164.2 W107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr3:183824396 C>T maps to NM_182589.2 H444H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr3:183824396 C>T maps to NM_182589.2 H444H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr4:113353567 G>C maps to NM_025144.3 G955G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr4:113353567 G>C maps to NM_025144.3 G955G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr5:7885831 C>T maps to NM_024010.2 Q335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr5:7885831 C>T maps to NM_024010.2 Q335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr5:160973364 C>G maps to NM_021911.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr5:160973364 C>G maps to NM_021911.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr5:161531031 G>T maps to NM_198903.2 G297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr5:161531031 G>T maps to NM_198903.2 G297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr5:176943152 C>A maps to NM_016222.2 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr5:176943152 C>A maps to NM_016222.2 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr7:38305105 C>A maps to ENST00000443402 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr7:38305105 C>A maps to ENST00000443402 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr7:55233025 C>T maps to NM_005228.3 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr7:55233025 C>T maps to NM_005228.3 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr7:72717905 G>A maps to NM_148956.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr7:72717905 G>A maps to NM_148956.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr7:75172175 C>A maps to NM_005338.4 E962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr7:75172175 C>A maps to NM_005338.4 E962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr7:107408303 C>T maps to NM_000111.2 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr7:107408303 C>T maps to NM_000111.2 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr9:116022566 C>T maps to NM_001859.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr9:116022566 C>T maps to NM_001859.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chrX:19983782 G>C maps to ENST00000379682 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chrX:19983782 G>C maps to ENST00000379682 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chrX:31947739 G>C maps to ENST00000357033 L2295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chrX:31947739 G>C maps to ENST00000357033 L2295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chrX:55479235 A>G maps to NM_014061.3 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chrX:55479235 A>G maps to NM_014061.3 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chrX:70347741 G>T did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chrX:70347741 G>T did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chrX:130678613 T>G maps to NM_001004486.1 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chrX:130678613 T>G maps to NM_001004486.1 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chrX:135431894 C>G maps to NM_153834.3 L2010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chrX:135431894 C>G maps to NM_153834.3 L2010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chrX:136649665 C>T maps to NM_003413.3 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chrX:136649665 C>T maps to NM_003413.3 F272F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chrX:142967282 A>G maps to NM_001012989.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chrX:142967282 A>G maps to NM_001012989.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chrX:149963726 G>A maps to ENST00000438086 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chrX:149963726 G>A maps to ENST00000438086 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chrX:154033633 C>T maps to NM_002436.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chrX:154033633 C>T maps to NM_002436.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr10:97987175 G>A maps to NM_013314.3 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr10:97987175 G>A maps to NM_013314.3 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr12:7025013 C>T maps to NM_001975.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr12:7025013 C>T maps to NM_001975.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr12:49176995 G>A maps to NM_015270.3 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr12:49176995 G>A maps to NM_015270.3 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr13:39262437 G>A maps to NM_207361.4 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr13:39262437 G>A maps to NM_207361.4 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr16:2905602 G>T maps to NM_022119.3 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr16:2905602 G>T maps to NM_022119.3 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr17:37371436 G>A maps to NM_198993.3 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr17:37371436 G>A maps to NM_198993.3 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr18:47101892 C>T maps to NM_006033.2 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr18:47101892 C>T maps to NM_006033.2 Y242Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr2:139429082 G>A maps to NM_007226.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr2:139429082 G>A maps to NM_007226.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr3:185363332 G>A maps to NM_006548.4 Q596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr3:185363332 G>A maps to NM_006548.4 Q596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr4:755158 G>A maps to NM_006315.4 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr4:755158 G>A maps to NM_006315.4 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr4:57896546 C>T maps to NM_000938.1 G1139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr4:57896546 C>T maps to NM_000938.1 G1139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr4:187517825 C>A maps to ENST00000260147 E4293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr4:187517825 C>A maps to ENST00000260147 E4293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr6:13230291 A>C maps to NM_030948.1 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr6:13230291 A>C maps to NM_030948.1 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr7:44747332 C>G maps to ENST00000444676 V998V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chr7:44747332 C>G maps to ENST00000444676 V998V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chrX:134483237 T>G maps to NM_152695.5 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7103-01A-21D-2012-08 chrX:134483237 T>G maps to NM_152695.5 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr1:9804037 G>C maps to NM_001009566.1 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr1:9804037 G>C maps to NM_001009566.1 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr1:77984358 G>T maps to NM_174858.1 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr1:77984358 G>T maps to NM_174858.1 E420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr1:153905171 G>A maps to NM_014856.2 D1235D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr1:153905171 G>A maps to NM_014856.2 D1235D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr1:240492662 C>A maps to ENST00000406993 I1587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr1:240492662 C>A maps to ENST00000406993 I1587I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr10:90665315 A>G maps to NM_020799.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr10:90665315 A>G maps to NM_020799.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr11:1956070 G>A maps to ENST00000397301 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr11:1956070 G>A maps to ENST00000397301 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr11:31312207 C>A maps to NM_181807.2 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr11:31312207 C>A maps to NM_181807.2 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr11:65396094 C>T maps to NM_032223.2 F1244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr11:65396094 C>T maps to NM_032223.2 F1244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr12:58021970 G>A maps to NM_001478.3 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr12:58021970 G>A maps to NM_001478.3 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr12:108618514 G>T did not map to a codon.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr12:108618514 G>T did not map to a codon.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr14:53010230 G>C maps to NM_020784.2 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr14:53010230 G>C maps to NM_020784.2 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr15:45047400 A>T maps to NM_182985.3 K104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr15:45047400 A>T maps to NM_182985.3 K104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr15:89864133 G>A maps to NM_002693.2 I948I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr15:89864133 G>A maps to NM_002693.2 I948I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr16:3406176 C>G maps to NM_012368.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr16:3406176 C>G maps to NM_012368.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr16:72094488 C>T maps to NM_005143.3 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr16:72094488 C>T maps to NM_005143.3 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr17:7577608 C>T did not map to a codon.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr17:7577608 C>T did not map to a codon.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr17:35800746 A>G maps to NM_001166105.1 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr17:35800746 A>G maps to NM_001166105.1 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr19:2810357 G>A maps to NM_003249.3 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr19:2810357 G>A maps to NM_003249.3 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr19:12734542 G>C maps to NM_153358.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr19:12734542 G>C maps to NM_153358.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr19:59028059 C>T maps to NM_032792.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr19:59028059 C>T maps to NM_032792.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr2:210518096 C>G maps to NM_002374.3 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr2:210518096 C>G maps to NM_002374.3 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr3:132166223 C>T maps to NM_015268.3 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr3:132166223 C>T maps to NM_015268.3 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr3:158363474 C>T maps to ENST00000264263 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr3:158363474 C>T maps to ENST00000264263 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr3:167183381 T>C maps to NM_006217.3 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr3:167183381 T>C maps to NM_006217.3 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr3:168838946 G>T maps to NM_004991.3 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr3:168838946 G>T maps to NM_004991.3 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr5:33576386 C>A maps to NM_030955.2 L1248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr5:33576386 C>A maps to NM_030955.2 L1248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr5:36066837 C>A maps to NM_174914.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr5:36066837 C>A maps to NM_174914.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr5:139781713 G>A maps to ENST00000253810 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr5:139781713 G>A maps to ENST00000253810 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr5:140789784 G>A maps to NM_018926.2 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr5:140789784 G>A maps to NM_018926.2 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr5:167850579 C>G maps to NM_001161661.1 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr5:167850579 C>G maps to NM_001161661.1 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr6:134495870 G>A maps to NM_005627.3 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr6:134495870 G>A maps to NM_005627.3 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr7:38357070 G>C maps to ENST00000444775 S8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr7:38357070 G>C maps to ENST00000444775 S8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr7:141673456 G>C maps to NM_176817.4 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr7:141673456 G>C maps to NM_176817.4 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr8:70570761 G>T maps to NM_001128206.1 E870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr8:70570761 G>T maps to NM_001128206.1 E870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr9:101552848 G>A maps to ENST00000375018 H133H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr9:101552848 G>A maps to ENST00000375018 H133H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chrX:50119799 G>A maps to NM_001013742.1 Q1076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chrX:50119799 G>A maps to NM_001013742.1 Q1076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr1:13936916 C>A maps to NM_006474.4 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr1:13936916 C>A maps to NM_006474.4 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr1:85666169 G>A maps to NM_032184.1 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr1:85666169 G>A maps to NM_032184.1 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr10:68687180 G>A maps to NM_178011.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr10:68687180 G>A maps to NM_178011.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr11:123597652 C>G maps to NM_003455.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr11:123597652 C>G maps to NM_003455.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr12:27824449 T>G maps to NM_003622.3 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr12:27824449 T>G maps to NM_003622.3 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr12:57975222 C>T maps to NM_004984.2 Y927Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr12:57975222 C>T maps to NM_004984.2 Y927Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr15:30011210 G>A maps to NM_003257.3 Y1045Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr15:30011210 G>A maps to NM_003257.3 Y1045Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr15:85164139 C>T maps to NM_181877.3 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr15:85164139 C>T maps to NM_181877.3 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr16:27237110 G>A maps to NM_145080.3 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr16:27237110 G>A maps to NM_145080.3 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr16:87724056 C>T maps to NM_020655.2 F697F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr16:87724056 C>T maps to NM_020655.2 F697F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr17:34340341 G>T maps to NM_005064.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr17:34340341 G>T maps to NM_005064.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr17:45820479 G>A maps to NM_013351.1 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr17:45820479 G>A maps to NM_013351.1 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr17:57958323 C>T maps to NM_016261.3 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr17:57958323 C>T maps to NM_016261.3 Q156Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr17:77753182 G>T maps to NM_005189.2 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr17:77753182 G>T maps to NM_005189.2 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr19:8436123 G>A did not map to a codon.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr19:8436123 G>A did not map to a codon.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr19:15272482 C>A maps to NM_000435.2 E1986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr19:15272482 C>A maps to NM_000435.2 E1986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr19:20807481 C>A maps to NM_001076675.2 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr19:20807481 C>A maps to NM_001076675.2 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr19:40030623 C>T maps to NM_153232.3 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr19:40030623 C>T maps to NM_153232.3 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr19:54678112 G>A maps to NM_024298.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr19:54678112 G>A maps to NM_024298.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr2:46605174 C>T maps to NM_001430.4 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr2:46605174 C>T maps to NM_001430.4 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr20:3605204 C>T maps to NM_139321.2 F1283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr20:3605204 C>T maps to NM_139321.2 F1283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr20:31023530 G>T maps to ENST00000375687 E1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr20:31023530 G>T maps to ENST00000375687 E1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr3:107497344 G>T maps to NM_001142568.1 E728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr3:107497344 G>T maps to NM_001142568.1 E728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr3:151545494 C>G maps to NM_001086.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr3:151545494 C>G maps to NM_001086.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr3:155200526 A>G maps to ENST00000340059 G1104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr3:155200526 A>G maps to ENST00000340059 G1104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr4:85752749 C>T maps to NM_014991.4 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr4:85752749 C>T maps to NM_014991.4 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr4:114823766 G>C maps to NM_024590.3 S488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr4:114823766 G>C maps to NM_024590.3 S488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr5:159520156 G>C maps to NM_001130864.1 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr5:159520156 G>C maps to NM_001130864.1 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr6:26032186 G>T maps to NM_003537.3 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr6:26032186 G>T maps to NM_003537.3 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr6:52268775 C>T maps to ENST00000361841 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr6:52268775 C>T maps to ENST00000361841 F260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr6:119341141 C>T did not map to a codon.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr6:119341141 C>T did not map to a codon.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr7:99002547 C>A maps to NM_014891.6 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr7:99002547 C>A maps to NM_014891.6 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr7:143806749 C>G maps to NM_001005480.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr7:143806749 C>G maps to NM_001005480.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr8:37702007 T>C maps to NM_018310.3 *420W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr8:37702007 T>C maps to NM_018310.3 *420W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr9:123632757 C>T maps to NM_015651.1 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chr9:123632757 C>T maps to NM_015651.1 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chrX:12734833 C>T maps to ENST00000429478 D742D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chrX:12734833 C>T maps to ENST00000429478 D742D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chrX:101971266 C>T maps to NM_138437.5 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chrX:101971266 C>T maps to NM_138437.5 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chrX:107978578 A>G maps to NM_003604.2 C332C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chrX:107978578 A>G maps to NM_003604.2 C332C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chrX:110644289 G>C maps to ENST00000358070 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chrX:110644289 G>C maps to ENST00000358070 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chrX:110979970 T>C maps to NM_001099922.2 A853A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chrX:110979970 T>C maps to NM_001099922.2 A853A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chrX:153698125 C>T maps to NM_017514.3 Y1598Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chrX:153698125 C>T maps to NM_017514.3 Y1598Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:91403925 G>A maps to NM_201269.1 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:91403925 G>A maps to NM_201269.1 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:91405605 C>T maps to NM_201269.1 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:91405605 C>T maps to NM_201269.1 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:110294747 G>A maps to NM_139053.1 Q436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:110294747 G>A maps to NM_139053.1 Q436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:120539637 C>A maps to NM_024408.2 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:120539637 C>A maps to NM_024408.2 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:147131782 T>C maps to NM_016361.3 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:147131782 T>C maps to NM_016361.3 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:159410090 T>C maps to NM_012351.2 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:159410090 T>C maps to NM_012351.2 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:161069389 G>A maps to NM_152366.4 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:161069389 G>A maps to NM_152366.4 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:200944026 C>T maps to NM_017596.2 A1530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:200944026 C>T maps to NM_017596.2 A1530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:205034930 G>A maps to NM_005076.3 G570G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:205034930 G>A maps to NM_005076.3 G570G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:223177960 C>T maps to NM_032890.2 F1074F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:223177960 C>T maps to NM_032890.2 F1074F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:228210571 C>T maps to ENST00000366753 H92H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr1:228210571 C>T maps to ENST00000366753 H92H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr10:70225524 G>A maps to NM_001080449.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr10:70225524 G>A maps to NM_001080449.1 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr11:9009123 G>A maps to NM_020645.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr11:9009123 G>A maps to NM_020645.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr11:64084792 G>A maps to NM_016404.1 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr11:64084792 G>A maps to NM_016404.1 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr12:40646774 C>T maps to NM_198578.3 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr12:40646774 C>T maps to NM_198578.3 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr14:20248699 C>G maps to NM_001005500.1 Y73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr14:20248699 C>G maps to NM_001005500.1 Y73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr14:24438078 G>C maps to NM_021004.2 *279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr14:24438078 G>C maps to NM_021004.2 *279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr15:40268784 G>A maps to NM_001013703.2 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr15:40268784 G>A maps to NM_001013703.2 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr15:40581115 G>A maps to NM_004573.2 Q1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr15:40581115 G>A maps to NM_004573.2 Q1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr15:74467615 C>T maps to NM_201526.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr15:74467615 C>T maps to NM_201526.1 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr15:97327424 C>T maps to NM_173499.3 C44C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr15:97327424 C>T maps to NM_173499.3 C44C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr17:4053284 C>T maps to NM_144611.3 H117H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr17:4053284 C>T maps to NM_144611.3 H117H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr19:6532807 G>A maps to NM_003811.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr19:6532807 G>A maps to NM_003811.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr19:54401268 C>T maps to NM_002739.3 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr19:54401268 C>T maps to NM_002739.3 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr19:56104199 C>T maps to NM_032836.2 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr19:56104199 C>T maps to NM_032836.2 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr2:27457393 G>A maps to NM_004341.3 Q1209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr2:27457393 G>A maps to NM_004341.3 Q1209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr2:65541018 C>T maps to NM_181784.2 Q291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr2:65541018 C>T maps to NM_181784.2 Q291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr2:74755570 C>A maps to ENST00000258081 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr2:74755570 C>A maps to ENST00000258081 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr2:198272766 T>C maps to NM_012433.2 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr2:198272766 T>C maps to NM_012433.2 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr2:220116736 C>T maps to NM_006000.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr2:220116736 C>T maps to NM_006000.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr20:368669 C>T maps to ENST00000422053 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr20:368669 C>T maps to ENST00000422053 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr22:41489078 C>A maps to NM_001429.3 S24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr22:41489078 C>A maps to NM_001429.3 S24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr3:10417305 C>T maps to NM_001001331.2 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr3:10417305 C>T maps to NM_001001331.2 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr3:183681280 G>A maps to NM_005688.2 D709D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr3:183681280 G>A maps to NM_005688.2 D709D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr4:1379682 C>T maps to NM_020894.2 A688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr4:1379682 C>T maps to NM_020894.2 A688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr4:187175917 G>A did not map to a codon.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr4:187175917 G>A did not map to a codon.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr5:16682097 C>T maps to NM_012334.2 T1357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr5:16682097 C>T maps to NM_012334.2 T1357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr7:36459870 C>T maps to NM_018685.2 R655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr7:36459870 C>T maps to NM_018685.2 R655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr7:44797688 C>G maps to NM_031449.3 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr7:44797688 C>G maps to NM_031449.3 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr7:63680526 A>G maps to NM_001159524.1 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr7:63680526 A>G maps to NM_001159524.1 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr7:120386012 T>C maps to NM_012281.2 H549H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr7:120386012 T>C maps to NM_012281.2 H549H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr7:142459767 C>G maps to ENST00000486171 S129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr7:142459767 C>G maps to ENST00000486171 S129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr8:95182706 T>C maps to NM_001144663.1 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr8:95182706 T>C maps to NM_001144663.1 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr8:145770918 C>T maps to NM_025251.1 E745E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr8:145770918 C>T maps to NM_025251.1 E745E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr9:37521757 G>A maps to NM_012166.2 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr9:37521757 G>A maps to NM_012166.2 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr9:129595075 C>T maps to NM_014007.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7178-01A-21D-2012-08 chr9:129595075 C>T maps to NM_014007.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr1:12331120 G>A maps to NM_015378.2 K681K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr1:12331120 G>A maps to NM_015378.2 K681K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr1:151149263 C>T maps to ENST00000354473 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr1:151149263 C>T maps to ENST00000354473 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr1:196918741 C>T maps to ENST00000367421 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr1:196918741 C>T maps to ENST00000367421 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr10:129839234 C>T maps to NM_006504.4 N30N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr10:129839234 C>T maps to NM_006504.4 N30N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr11:130275559 G>A maps to NM_007037.4 R855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr11:130275559 G>A maps to NM_007037.4 R855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr12:109696114 G>T maps to NM_001093.3 R2102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr12:109696114 G>T maps to NM_001093.3 R2102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr14:75469993 G>T maps to NM_014239.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr14:75469993 G>T maps to NM_014239.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr15:80181636 T>C maps to NM_006441.3 Q59Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr15:80181636 T>C maps to NM_006441.3 Q59Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr15:90168445 C>A maps to NM_152259.3 G1635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr15:90168445 C>A maps to NM_152259.3 G1635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr17:72791737 C>T maps to NM_017728.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr17:72791737 C>T maps to NM_017728.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr18:56171232 C>T maps to NM_052947.3 Q2059Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr18:56171232 C>T maps to NM_052947.3 Q2059Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr19:58983226 G>A maps to NM_014347.2 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr19:58983226 G>A maps to NM_014347.2 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr2:27480852 G>T maps to NM_003459.4 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr2:27480852 G>T maps to NM_003459.4 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr2:152534282 G>A maps to NM_001164507.1 N1190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr2:152534282 G>A maps to NM_001164507.1 N1190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr5:19721468 G>A maps to NM_004934.3 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr5:19721468 G>A maps to NM_004934.3 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr5:141334956 C>T maps to NM_016580.2 P820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr5:141334956 C>T maps to NM_016580.2 P820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr7:30485827 G>A maps to NM_006092.2 N794N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr7:30485827 G>A maps to NM_006092.2 N794N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr7:92987684 C>T maps to NM_017667.2 I944I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr7:92987684 C>T maps to NM_017667.2 I944I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr7:146829389 C>T maps to NM_014141.5 N379N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr7:146829389 C>T maps to NM_014141.5 N379N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr9:96418258 C>T maps to NM_005392.3 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7180-01A-11D-2012-08 chr9:96418258 C>T maps to NM_005392.3 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr1:4829976 C>T maps to NM_018836.3 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr1:4829976 C>T maps to NM_018836.3 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr1:207109002 C>T maps to NM_002644.3 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr1:207109002 C>T maps to NM_002644.3 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr12:49415845 G>A maps to NM_003482.3 R5501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr12:49415845 G>A maps to NM_003482.3 R5501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr13:70549903 A>C maps to NM_020866.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr13:70549903 A>C maps to NM_020866.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr13:98828824 G>A maps to NM_178861.4 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr13:98828824 G>A maps to NM_178861.4 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr14:21863098 C>A maps to NM_001170629.1 E1788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr14:21863098 C>A maps to NM_001170629.1 E1788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr15:42109604 C>T maps to NM_001128608.1 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr15:42109604 C>T maps to NM_001128608.1 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr15:43771644 C>T maps to NM_001141980.1 Q246Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr15:43771644 C>T maps to NM_001141980.1 Q246Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr16:27504018 C>T maps to NM_001520.3 S964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr16:27504018 C>T maps to NM_001520.3 S964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr16:67264613 C>T maps to NM_013241.2 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr16:67264613 C>T maps to NM_013241.2 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr17:42855360 G>A maps to NM_002390.4 W704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr17:42855360 G>A maps to NM_002390.4 W704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr19:8174521 G>T maps to NM_032447.3 G1483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr19:8174521 G>T maps to NM_032447.3 G1483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr19:55107314 C>T maps to NM_006863.1 Y291Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr19:55107314 C>T maps to NM_006863.1 Y291Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr2:223918015 C>T maps to NM_080671.2 N156N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr2:223918015 C>T maps to NM_080671.2 N156N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr4:39978104 C>T maps to NM_001100399.1 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr4:39978104 C>T maps to NM_001100399.1 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr4:113347689 G>T maps to NM_025144.3 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr4:113347689 G>T maps to NM_025144.3 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr4:146770711 C>T maps to ENST00000508784 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr4:146770711 C>T maps to ENST00000508784 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr4:187629107 G>T maps to ENST00000260147 S625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr4:187629107 G>T maps to ENST00000260147 S625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr5:174869349 G>A maps to NM_000794.3 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr5:174869349 G>A maps to NM_000794.3 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr6:42796800 C>T maps to NM_015349.1 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr6:42796800 C>T maps to NM_015349.1 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr7:136699800 C>T maps to NM_001006628.1 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr7:136699800 C>T maps to NM_001006628.1 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr11:92615996 G>T maps to ENST00000298047 T4125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr11:92615996 G>T maps to ENST00000298047 T4125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr2:15468388 T>C maps to NM_015909.2 E1465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7183-01A-11D-2012-08 chr2:15468388 T>C maps to NM_015909.2 E1465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:17552555 G>C maps to NM_013358.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:17552555 G>C maps to NM_013358.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:44156524 G>T maps to NM_014663.2 G683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:44156524 G>T maps to NM_014663.2 G683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:51439743 G>C maps to NM_078626.2 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:51439743 G>C maps to NM_078626.2 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:152085380 G>A maps to NM_007113.2 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:152085380 G>A maps to NM_007113.2 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:152671631 C>T maps to NM_178428.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:152671631 C>T maps to NM_178428.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:155744942 G>A maps to ENST00000368331 Q734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:155744942 G>A maps to ENST00000368331 Q734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:161677050 C>T maps to NM_001184866.1 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:161677050 C>T maps to NM_001184866.1 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:175097244 T>G maps to NM_022093.1 L1041L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:175097244 T>G maps to NM_022093.1 L1041L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr12:8693385 G>T maps to NM_014358.2 S3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr12:8693385 G>T maps to NM_014358.2 S3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr12:13243617 G>A maps to NM_001080555.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr12:13243617 G>A maps to NM_001080555.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr12:57167653 G>A maps to NM_003725.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr12:57167653 G>A maps to NM_003725.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr12:65461538 G>C maps to NM_007191.4 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr12:65461538 G>C maps to NM_007191.4 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr12:104063401 A>G maps to NM_017564.9 G752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr12:104063401 A>G maps to NM_017564.9 G752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr12:123200717 G>A maps to NM_006018.2 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr12:123200717 G>A maps to NM_006018.2 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr15:23006378 G>A maps to NM_030922.6 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr15:23006378 G>A maps to NM_030922.6 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr15:74284509 G>A maps to NM_004809.3 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr15:74284509 G>A maps to NM_004809.3 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr17:43246701 A>G maps to NM_144608.1 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr17:43246701 A>G maps to NM_144608.1 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr17:61958487 C>T maps to NM_002059.3 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr17:61958487 C>T maps to NM_002059.3 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr17:80211117 G>A maps to NM_001893.3 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr17:80211117 G>A maps to NM_001893.3 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr18:42530734 C>A maps to NM_015559.2 S477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr18:42530734 C>A maps to NM_015559.2 S477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr18:46889583 A>T maps to NM_017653.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr18:46889583 A>T maps to NM_017653.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr19:7619912 C>T maps to NM_001166111.1 H933H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr19:7619912 C>T maps to NM_001166111.1 H933H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr2:101097598 G>A maps to NM_001011717.1 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr2:101097598 G>A maps to NM_001011717.1 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr2:215440474 T>C maps to NM_001080500.2 C200C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr2:215440474 T>C maps to NM_001080500.2 C200C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr2:241492384 G>A maps to ENST00000401804 Y142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr2:241492384 G>A maps to ENST00000401804 Y142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr20:4680246 C>A maps to NM_001080123.1 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr20:4680246 C>A maps to NM_001080123.1 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr4:89583676 C>T maps to NM_014606.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr4:89583676 C>T maps to NM_014606.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr4:110980840 T>G maps to NM_024090.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr4:110980840 T>G maps to NM_024090.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr4:114095603 C>A maps to NM_001148.4 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr4:114095603 C>A maps to NM_001148.4 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr5:52201635 C>G maps to NM_181501.1 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr5:52201635 C>G maps to NM_181501.1 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr5:66459359 G>A maps to NM_001164664.1 S1451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr5:66459359 G>A maps to NM_001164664.1 S1451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr5:139903728 G>T maps to ENST00000253810 E1466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr5:139903728 G>T maps to ENST00000253810 E1466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr6:29796425 G>T maps to ENST00000376828 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr6:29796425 G>T maps to ENST00000376828 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr6:30698342 C>G did not map to a codon.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr6:30698342 C>G did not map to a codon.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr6:35436735 G>T maps to NM_007104.4 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr6:35436735 G>T maps to NM_007104.4 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr6:70386389 G>A maps to NM_018368.3 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr6:70386389 G>A maps to NM_018368.3 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr6:150174186 G>A maps to NM_032832.5 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr6:150174186 G>A maps to NM_032832.5 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr6:151694703 C>T maps to NM_020861.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr6:151694703 C>T maps to NM_020861.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr7:82545295 A>G maps to NM_033026.5 L4002L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr7:82545295 A>G maps to NM_033026.5 L4002L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr7:89854671 T>C maps to NM_152999.3 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr7:89854671 T>C maps to NM_152999.3 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr7:92761381 C>T maps to NM_152703.2 R1301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr7:92761381 C>T maps to NM_152703.2 R1301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr7:98984356 C>T maps to NM_005720.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr7:98984356 C>T maps to NM_005720.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr7:142564287 C>T maps to NM_004445.3 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr7:142564287 C>T maps to NM_004445.3 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr8:95531704 C>G did not map to a codon.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr8:95531704 C>G did not map to a codon.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr9:77286706 C>A maps to ENST00000396204 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr9:77286706 C>A maps to ENST00000396204 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr9:116136604 C>T maps to NM_031219.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr9:116136604 C>T maps to NM_031219.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr9:119461760 C>T maps to NM_012210.3 G580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr9:119461760 C>T maps to NM_012210.3 G580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr9:130684359 C>G maps to NM_001135219.1 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr9:130684359 C>G maps to NM_001135219.1 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr9:140137605 G>A maps to NM_006088.5 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr9:140137605 G>A maps to NM_006088.5 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chrX:34148618 C>A maps to NM_203408.3 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chrX:34148618 C>A maps to NM_203408.3 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr15:72608203 C>T maps to NM_052840.4 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr15:72608203 C>T maps to NM_052840.4 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr1:152188023 C>T maps to NM_001009931.1 S2027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr1:152188023 C>T maps to NM_001009931.1 S2027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr10:96014689 C>A maps to ENST00000371380 S1146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr10:96014689 C>A maps to ENST00000371380 S1146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr11:6977594 C>T maps to NM_013250.2 Q463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr11:6977594 C>T maps to NM_013250.2 Q463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr11:64572116 G>A maps to NM_130804.2 Q513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr11:64572116 G>A maps to NM_130804.2 Q513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr12:101988803 G>A did not map to a codon.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr12:101988803 G>A did not map to a codon.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr13:25875964 C>T maps to NM_014089.3 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr13:25875964 C>T maps to NM_014089.3 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr13:92346020 C>T maps to NM_004466.4 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr13:92346020 C>T maps to NM_004466.4 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr14:74757039 C>T maps to NM_005050.3 K427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr14:74757039 C>T maps to NM_005050.3 K427K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr15:40954308 C>T maps to NM_170589.3 L2318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr15:40954308 C>T maps to NM_170589.3 L2318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr15:89698751 C>T maps to NM_152924.4 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr15:89698751 C>T maps to NM_152924.4 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr18:70532112 T>C maps to NM_153181.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr18:70532112 T>C maps to NM_153181.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr19:12866478 C>T maps to NM_017682.2 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr19:12866478 C>T maps to NM_017682.2 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr19:42847638 G>A maps to ENST00000251268 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr19:42847638 G>A maps to ENST00000251268 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr19:42914527 G>C maps to NM_005357.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr19:42914527 G>C maps to NM_005357.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr19:50805051 C>T maps to NM_001145809.1 A1868A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr19:50805051 C>T maps to NM_001145809.1 A1868A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr19:55670684 G>A maps to ENST00000301249 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr19:55670684 G>A maps to ENST00000301249 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr22:21799897 C>T maps to NM_015094.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr22:21799897 C>T maps to NM_015094.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr22:24982180 C>T maps to NM_207644.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr22:24982180 C>T maps to NM_207644.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr3:369939 C>T maps to NM_006614.2 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr3:369939 C>T maps to NM_006614.2 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr3:167240196 T>A maps to NM_178824.3 K542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr3:167240196 T>A maps to NM_178824.3 K542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr4:160251523 G>A maps to NM_014247.2 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr4:160251523 G>A maps to NM_014247.2 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr4:174449918 G>A maps to NM_021973.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr4:174449918 G>A maps to NM_021973.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr7:72418900 G>A maps to ENST00000446813 P964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr7:72418900 G>A maps to ENST00000446813 P964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr7:150094921 C>T maps to NM_173680.3 C451C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr7:150094921 C>T maps to NM_173680.3 C451C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr8:76471034 G>A did not map to a codon.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr8:76471034 G>A did not map to a codon.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr9:99521422 C>T maps to NM_014930.1 Q563Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr9:99521422 C>T maps to NM_014930.1 Q563Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr9:131019938 G>T maps to NM_004486.4 R860R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7236-01A-11D-2012-08 chr9:131019938 G>T maps to NM_004486.4 R860R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr1:27100151 G>A maps to NM_006015.4 S1316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr1:27100151 G>A maps to NM_006015.4 S1316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr1:150416839 C>G maps to NM_015203.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr1:150416839 C>G maps to NM_015203.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr10:89692804 C>T maps to NM_000314.4 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr10:89692804 C>T maps to NM_000314.4 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr11:116661094 G>A maps to NM_052968.4 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr11:116661094 G>A maps to NM_052968.4 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr11:134038397 G>A maps to NM_015261.2 F1113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr11:134038397 G>A maps to NM_015261.2 F1113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr13:113479842 G>A maps to NM_032189.3 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr13:113479842 G>A maps to NM_032189.3 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr14:29237513 C>T maps to NM_005249.3 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr14:29237513 C>T maps to NM_005249.3 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr16:22161161 G>A maps to NM_173615.3 V1013V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr16:22161161 G>A maps to NM_173615.3 V1013V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr17:48631732 C>T maps to NM_022827.2 S693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr17:48631732 C>T maps to NM_022827.2 S693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr19:53855451 A>G maps to NM_138374.1 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr19:53855451 A>G maps to NM_138374.1 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr3:74350657 T>A maps to NM_020872.1 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr3:74350657 T>A maps to NM_020872.1 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr3:129695950 C>T maps to NM_007117.3 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr3:129695950 C>T maps to NM_007117.3 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr3:197402347 C>T maps to NM_014687.1 Q895Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr3:197402347 C>T maps to NM_014687.1 Q895Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr5:102612012 A>G maps to NM_033211.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr5:102612012 A>G maps to NM_033211.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr5:150924338 G>A maps to NM_001447.2 R2117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr5:150924338 G>A maps to NM_001447.2 R2117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr5:171520514 C>T maps to NM_005990.3 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr5:171520514 C>T maps to NM_005990.3 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr6:32032667 C>T maps to ENST00000375244 K2257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr6:32032667 C>T maps to ENST00000375244 K2257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr6:51920456 G>A maps to NM_138694.3 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr6:51920456 G>A maps to NM_138694.3 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr7:33185887 T>C maps to NM_198428.2 D8D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr7:33185887 T>C maps to NM_198428.2 D8D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr7:89915640 C>G maps to NM_001039706.2 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr7:89915640 C>G maps to NM_001039706.2 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr7:142919245 C>T maps to NM_176882.1 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr7:142919245 C>T maps to NM_176882.1 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr9:121929388 C>T maps to NM_014618.2 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr9:121929388 C>T maps to NM_014618.2 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr9:139407532 G>A maps to NM_017617.3 Q803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr9:139407532 G>A maps to NM_017617.3 Q803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr9:140611324 C>T maps to NM_024757.4 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chr9:140611324 C>T maps to NM_024757.4 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chrX:63410342 G>A maps to NM_152424.3 R942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chrX:63410342 G>A maps to NM_152424.3 R942*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chrX:69510346 G>A maps to NM_012310.4 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chrX:69510346 G>A maps to NM_012310.4 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chrX:135754233 C>A maps to NM_004840.2 E694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7238-01A-11D-2012-08 chrX:135754233 C>A maps to NM_004840.2 E694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr1:43803900 C>A maps to NM_005373.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr1:43803900 C>A maps to NM_005373.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr1:89523673 C>A did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr1:89523673 C>A did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr1:157514693 A>C maps to NM_031281.2 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr1:157514693 A>C maps to NM_031281.2 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr1:166904661 A>T maps to NM_199351.2 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr1:166904661 A>T maps to NM_199351.2 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr1:197396758 G>A maps to NM_201253.2 E768E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr1:197396758 G>A maps to NM_201253.2 E768E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr1:203472811 C>T maps to NM_014359.3 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr1:203472811 C>T maps to NM_014359.3 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr1:214171293 C>A maps to NM_002763.3 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr1:214171293 C>A maps to NM_002763.3 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr10:62648687 T>A maps to NM_014836.4 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr10:62648687 T>A maps to NM_014836.4 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr10:79163661 C>A maps to NM_001161352.1 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr10:79163661 C>A maps to NM_001161352.1 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr10:102089668 G>T maps to NM_016112.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr10:102089668 G>T maps to NM_016112.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr10:124339337 C>T maps to ENST00000368915 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr10:124339337 C>T maps to ENST00000368915 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:4935986 G>A maps to NM_001005238.1 Q303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:4935986 G>A maps to NM_001005238.1 Q303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:30253577 C>T maps to NM_001018080.1 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:30253577 C>T maps to NM_001018080.1 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:56468408 C>T maps to NM_001013358.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:56468408 C>T maps to NM_001013358.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:67275065 C>A maps to NM_005851.3 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:67275065 C>A maps to NM_005851.3 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:89902134 T>A maps to NM_005467.3 Y439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:89902134 T>A maps to NM_005467.3 Y439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:108383614 C>A maps to NM_015065.2 S873S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:108383614 C>A maps to NM_015065.2 S873S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:113630935 G>C maps to NM_004724.2 S192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:113630935 G>C maps to NM_004724.2 S192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:117869497 C>A maps to NM_001558.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:117869497 C>A maps to NM_001558.3 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:118850288 C>G maps to NM_181721.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr11:118850288 C>G maps to NM_181721.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:309925 G>T maps to NM_003044.3 S201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:309925 G>T maps to NM_003044.3 S201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:10279170 T>A maps to NM_197947.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:10279170 T>A maps to NM_197947.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:10319425 C>T maps to NM_002543.3 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:10319425 C>T maps to NM_002543.3 K103K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:21457427 G>T maps to NM_134431.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:21457427 G>T maps to NM_134431.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:52115637 G>T maps to NM_014191.2 V648V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:52115637 G>T maps to NM_014191.2 V648V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:54115879 G>A maps to NM_020898.2 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:54115879 G>A maps to NM_020898.2 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:60169128 T>C maps to NM_004731.3 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:60169128 T>C maps to NM_004731.3 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:88487639 C>A maps to NM_025114.3 R1072R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:88487639 C>A maps to NM_025114.3 R1072R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:99793502 T>A maps to NM_152788.3 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:99793502 T>A maps to NM_152788.3 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:101442141 A>T maps to ENST00000392977 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:101442141 A>T maps to ENST00000392977 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:112605240 C>G maps to NM_001109662.2 P3966P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:112605240 C>G maps to NM_001109662.2 P3966P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:113541857 G>T maps to NM_001193520.1 S667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:113541857 G>T maps to NM_001193520.1 S667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:122396264 G>A maps to NM_144668.4 K606K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:122396264 G>A maps to NM_144668.4 K606K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:133682775 G>T maps to NM_003440.2 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr12:133682775 G>T maps to NM_003440.2 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr13:46661881 C>A maps to NM_001872.3 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr13:46661881 C>A maps to NM_001872.3 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr14:91084370 C>T maps to NM_001010854.1 V590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr14:91084370 C>T maps to NM_001010854.1 V590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr14:105410213 G>A maps to NM_138420.2 A3858A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr14:105410213 G>A maps to NM_138420.2 A3858A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr15:23811309 C>G maps to NM_005664.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr15:23811309 C>G maps to NM_005664.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr15:27185147 C>G maps to NM_000810.3 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr15:27185147 C>G maps to NM_000810.3 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr15:34646692 G>C maps to ENST00000438749 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr15:34646692 G>C maps to ENST00000438749 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr15:88669547 G>A maps to NM_001012338.1 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr15:88669547 G>A maps to NM_001012338.1 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr15:99251052 C>A maps to NM_000875.3 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr15:99251052 C>A maps to NM_000875.3 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr16:75513528 G>C maps to NM_021615.4 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr16:75513528 G>C maps to NM_021615.4 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr16:77353778 C>G maps to NM_199355.2 A833A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr16:77353778 C>G maps to NM_199355.2 A833A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr17:45901756 C>T maps to NM_145255.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr17:45901756 C>T maps to NM_145255.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr17:51901020 G>C maps to NM_032559.4 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr17:51901020 G>C maps to NM_032559.4 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr17:79589282 G>A maps to NM_017921.2 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr17:79589282 G>A maps to NM_017921.2 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr18:31226288 G>A maps to NM_030632.1 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr18:31226288 G>A maps to NM_030632.1 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr19:12991694 C>G did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr19:12991694 C>G did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr19:54515286 G>T maps to NM_145814.1 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr19:54515286 G>T maps to NM_145814.1 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr19:54646739 G>T did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr19:54646739 G>T did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:20647663 C>A maps to NM_004040.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:20647663 C>A maps to NM_004040.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:42580402 C>A maps to NM_004718.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:42580402 C>A maps to NM_004718.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:44104828 T>A did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:44104828 T>A did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:50780106 T>A maps to ENST00000404971 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:50780106 T>A maps to ENST00000404971 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:128036884 A>G maps to NM_000122.1 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:128036884 A>G maps to NM_000122.1 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:179411787 A>T maps to NM_133378.4 A28920A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:179411787 A>T maps to NM_133378.4 A28920A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:179581891 G>T maps to NM_133378.4 A7279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:179581891 G>T maps to NM_133378.4 A7279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:203747436 T>C maps to NM_018256.3 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:203747436 T>C maps to NM_018256.3 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:206869166 A>G maps to NM_017759.4 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:206869166 A>G maps to NM_017759.4 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:220501487 C>T maps to NM_201574.2 A836A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:220501487 C>T maps to NM_201574.2 A836A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:233246045 C>T maps to NM_001632.3 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:233246045 C>T maps to NM_001632.3 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:241831031 G>T maps to NM_001085437.1 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr2:241831031 G>T maps to NM_001085437.1 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr20:2640690 G>A maps to NM_006899.2 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr20:2640690 G>A maps to NM_006899.2 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr22:45689059 A>T did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr22:45689059 A>T did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr3:14769944 G>T did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr3:14769944 G>T did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr3:109049490 C>A maps to NM_018189.3 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr3:109049490 C>A maps to NM_018189.3 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr3:130287206 C>A maps to NM_001102608.1 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr3:130287206 C>A maps to NM_001102608.1 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr4:8037889 G>A maps to NM_001130083.1 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr4:8037889 G>A maps to NM_001130083.1 Q345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr4:89414185 G>A maps to NM_016323.2 G719G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr4:89414185 G>A maps to NM_016323.2 G719G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr4:187120146 C>T maps to NM_207352.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr4:187120146 C>T maps to NM_207352.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr5:110819998 G>A maps to NM_001744.4 K419K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr5:110819998 G>A maps to NM_001744.4 K419K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr5:140207984 C>T maps to NM_018909.2 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr5:140207984 C>T maps to NM_018909.2 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr5:140346944 G>A maps to NM_018899.5 K198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr5:140346944 G>A maps to NM_018899.5 K198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr5:148407521 C>A maps to NM_024577.3 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr5:148407521 C>A maps to NM_024577.3 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr6:28543799 T>A maps to NM_052923.1 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr6:28543799 T>A maps to NM_052923.1 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr6:36294356 C>T maps to NM_001010903.4 W322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr6:36294356 C>T maps to NM_001010903.4 W322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr6:129802529 G>A maps to NM_000426.3 L2565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr6:129802529 G>A maps to NM_000426.3 L2565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr6:133013715 G>T maps to NM_004666.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr6:133013715 G>T maps to NM_004666.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr7:1515968 G>A maps to ENST00000389470 I1972I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr7:1515968 G>A maps to ENST00000389470 I1972I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr7:91724386 T>G maps to NM_005751.4 L3210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr7:91724386 T>G maps to NM_005751.4 L3210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr7:121756933 T>A maps to NM_005763.3 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr7:121756933 T>A maps to NM_005763.3 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr7:146829567 C>T maps to NM_014141.5 Q439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr7:146829567 C>T maps to NM_014141.5 Q439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr7:151845955 C>T maps to ENST00000355193 W4409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr7:151845955 C>T maps to ENST00000355193 W4409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr8:144459585 G>T maps to ENST00000422773 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr8:144459585 G>T maps to ENST00000422773 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chrX:3229298 C>T maps to NM_015419.3 G2315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chrX:3229298 C>T maps to NM_015419.3 G2315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chrX:12939288 T>C maps to ENST00000311912 F728F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chrX:12939288 T>C maps to ENST00000311912 F728F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chrX:34960983 C>A maps to NM_152631.2 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chrX:34960983 C>A maps to NM_152631.2 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chrX:50119164 C>A did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chrX:50119164 C>A did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chrX:89177111 G>T maps to NM_138960.3 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chrX:89177111 G>T maps to NM_138960.3 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chrX:117817177 C>T maps to ENST00000276204 Q2034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chrX:117817177 C>T maps to ENST00000276204 Q2034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chrX:153533682 T>A maps to NM_012253.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chrX:153533682 T>A maps to NM_012253.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr12:56866514 C>G maps to NM_013267.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr12:56866514 C>G maps to NM_013267.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr14:23746121 G>A maps to NM_020834.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr14:23746121 G>A maps to NM_020834.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr15:43820774 C>T maps to ENST00000382031 N2606N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr15:43820774 C>T maps to ENST00000382031 N2606N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr16:70597895 G>A maps to NM_012426.4 T802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr16:70597895 G>A maps to NM_012426.4 T802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr17:57287433 C>T maps to NM_018149.6 R8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr17:57287433 C>T maps to NM_018149.6 R8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:1244102 C>T maps to NM_001687.4 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:1244102 C>T maps to NM_001687.4 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:2234192 G>A maps to NM_018049.1 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:2234192 G>A maps to NM_018049.1 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:13395973 C>T maps to NM_023035.2 E1204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:13395973 C>T maps to NM_023035.2 E1204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:38980888 C>T maps to NM_000540.2 R1996R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:38980888 C>T maps to NM_000540.2 R1996R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:49458946 C>T maps to NM_138761.3 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:49458946 C>T maps to NM_138761.3 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:49962337 G>A maps to NM_153329.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:49962337 G>A maps to NM_153329.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:54416118 C>T maps to NM_031896.4 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr19:54416118 C>T maps to NM_031896.4 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr2:5833120 C>T maps to NM_003108.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr2:5833120 C>T maps to NM_003108.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr21:22804479 G>A maps to NM_004540.2 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr21:22804479 G>A maps to NM_004540.2 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr3:14499523 C>T maps to NM_001134367.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr3:14499523 C>T maps to NM_001134367.1 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr4:41265297 C>T maps to NM_004181.4 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr4:41265297 C>T maps to NM_004181.4 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr4:121958732 A>G maps to NM_024574.3 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr4:121958732 A>G maps to NM_024574.3 N131N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr4:134072410 G>A maps to NM_032961.1 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr4:134072410 G>A maps to NM_032961.1 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr4:139965865 C>T maps to NM_012118.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr4:139965865 C>T maps to NM_012118.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr6:143092671 C>T maps to NM_006734.3 T1068T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr6:143092671 C>T maps to NM_006734.3 T1068T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr6:144769777 C>T maps to NM_007124.2 Q649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr6:144769777 C>T maps to NM_007124.2 Q649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr7:154681010 G>A maps to NM_130797.2 A778A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr7:154681010 G>A maps to NM_130797.2 A778A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7243-01A-11D-2012-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:12418559 G>T maps to NM_015378.2 P3348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:12418559 G>T maps to NM_015378.2 P3348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:22179292 C>T maps to NM_005529.5 V2208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:22179292 C>T maps to NM_005529.5 V2208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:26138255 C>T maps to NM_020451.2 H389H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:26138255 C>T maps to NM_020451.2 H389H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:44058189 C>G maps to NM_002840.3 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:44058189 C>G maps to NM_002840.3 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:48764464 C>A maps to NM_019073.2 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:48764464 C>A maps to NM_019073.2 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:76365338 C>G maps to NM_002440.2 S856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:76365338 C>G maps to NM_002440.2 S856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:145368632 G>T maps to NM_001039703.4 T3537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:145368632 G>T maps to NM_001039703.4 T3537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:153430419 G>T maps to NM_002963.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:153430419 G>T maps to NM_002963.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:207105831 C>A maps to NM_002644.3 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:207105831 C>A maps to NM_002644.3 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:237796939 A>T maps to NM_001035.2 I2206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:237796939 A>T maps to NM_001035.2 I2206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:247587341 C>T maps to NM_004895.4 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:247587341 C>T maps to NM_004895.4 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:47087814 C>G maps to NM_005972.4 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:47087814 C>G maps to NM_005972.4 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:55568469 A>T maps to NM_001142769.1 G1785G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:55568469 A>T maps to NM_001142769.1 G1785G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:61830609 T>C maps to NM_020987.2 Q3343Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:61830609 T>C maps to NM_020987.2 Q3343Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:69571400 G>A maps to NM_021800.2 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:69571400 G>A maps to NM_021800.2 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:81050777 G>C maps to NM_020338.3 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:81050777 G>C maps to NM_020338.3 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:84498356 C>A maps to ENST00000404547 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:84498356 C>A maps to ENST00000404547 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:102749398 A>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:102749398 A>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:131639252 G>T maps to ENST00000355311 Y472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr10:131639252 G>T maps to ENST00000355311 Y472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:5172864 A>G maps to NM_012375.2 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:5172864 A>G maps to NM_012375.2 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:5364184 G>T maps to NM_001005567.1 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:5364184 G>T maps to NM_001005567.1 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:9466671 A>C maps to NM_006391.2 G1016G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:9466671 A>C maps to NM_006391.2 G1016G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:55703378 A>G maps to NM_006637.1 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:55703378 A>G maps to NM_006637.1 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:56020199 C>T maps to NM_001004747.1 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:56020199 C>T maps to NM_001004747.1 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:56127928 T>C maps to NM_001005205.1 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:56127928 T>C maps to NM_001005205.1 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:56309851 T>C maps to NM_001005245.1 K294K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:56309851 T>C maps to NM_001005245.1 K294K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:68177398 C>T maps to NM_002335.2 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:68177398 C>T maps to NM_002335.2 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:68540780 C>T maps to NM_001876.3 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:68540780 C>T maps to NM_001876.3 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:104819392 C>A maps to NM_001225.3 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:104819392 C>A maps to NM_001225.3 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:105950302 C>G maps to NM_015423.2 S98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:105950302 C>G maps to NM_015423.2 S98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:118772309 C>A maps to NM_182557.2 A714A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:118772309 C>A maps to NM_182557.2 A714A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:126283416 G>C maps to ENST00000356132 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr11:126283416 G>C maps to ENST00000356132 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:4835950 C>T maps to NM_017417.1 N155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:4835950 C>T maps to NM_017417.1 N155N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:5021761 C>T maps to NM_000217.2 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:5021761 C>T maps to NM_000217.2 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:10147806 G>T maps to NM_016509.3 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:10147806 G>T maps to NM_016509.3 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:20769240 T>C maps to NM_000921.3 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:20769240 T>C maps to NM_000921.3 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:52756640 G>T maps to NM_002283.3 C358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:52756640 G>T maps to NM_002283.3 C358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:88478551 C>G maps to NM_025114.3 L1505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:88478551 C>G maps to NM_025114.3 L1505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:93101489 G>T maps to NM_001037671.3 *191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:93101489 G>T maps to NM_001037671.3 *191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:96641259 A>C maps to NM_005230.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:96641259 A>C maps to NM_005230.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:110230483 C>A maps to NM_021625.4 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:110230483 C>A maps to NM_021625.4 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:122825884 T>A maps to ENST00000302528 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr12:122825884 T>A maps to ENST00000302528 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr13:45725937 A>G maps to NM_004128.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr13:45725937 A>G maps to NM_004128.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr13:100193873 C>A maps to NM_004800.1 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr13:100193873 C>A maps to NM_004800.1 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr14:24108189 C>A maps to NM_182908.4 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr14:24108189 C>A maps to NM_182908.4 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr14:24641796 C>T maps to NM_005132.2 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr14:24641796 C>T maps to NM_005132.2 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr14:47504487 A>T maps to NM_001113498.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr14:47504487 A>T maps to NM_001113498.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr14:77274327 G>A maps to NM_015305.3 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr14:77274327 G>A maps to NM_015305.3 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr14:94914814 G>T maps to NM_001080451.1 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr14:94914814 G>T maps to NM_001080451.1 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr14:99641174 G>A maps to NM_138576.2 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr14:99641174 G>A maps to NM_138576.2 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr14:103416153 C>A maps to NM_006035.3 E1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr14:103416153 C>A maps to NM_006035.3 E1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr15:58458910 C>T maps to NM_020980.3 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr15:58458910 C>T maps to NM_020980.3 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr15:80988171 G>T maps to NM_021214.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr15:80988171 G>T maps to NM_021214.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr16:4861227 G>T maps to NM_032569.3 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr16:4861227 G>T maps to NM_032569.3 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr16:19488759 A>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr16:19488759 A>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr16:56899254 C>T maps to NM_000339.2 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr16:56899254 C>T maps to NM_000339.2 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr16:56917997 G>T maps to NM_000339.2 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr16:56917997 G>T maps to NM_000339.2 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr16:68591908 G>A maps to NM_133458.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr16:68591908 G>A maps to NM_133458.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr17:2604688 G>A maps to NM_015229.3 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr17:2604688 G>A maps to NM_015229.3 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr17:12916587 C>A maps to NM_018127.6 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr17:12916587 C>A maps to NM_018127.6 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr17:40970593 G>C maps to NM_003766.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr17:40970593 G>C maps to NM_003766.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr17:73738819 C>T maps to NM_001005619.1 N980N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr17:73738819 C>T maps to NM_001005619.1 N980N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr17:78321974 G>A maps to NM_020914.4 A3329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr17:78321974 G>A maps to NM_020914.4 A3329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr18:55368509 G>A maps to NM_005603.4 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr18:55368509 G>A maps to NM_005603.4 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr18:77896154 G>C maps to NM_014913.3 P953P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr18:77896154 G>C maps to NM_014913.3 P953P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:6442072 G>T maps to NM_024103.2 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:6442072 G>T maps to NM_024103.2 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:9071209 T>C maps to NM_024690.2 T5412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:9071209 T>C maps to NM_024690.2 T5412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:18004622 T>A maps to NM_000453.2 A623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:18004622 T>A maps to NM_000453.2 A623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:18179337 T>A did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:18179337 T>A did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:30935395 T>A maps to NM_014717.1 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:30935395 T>A maps to NM_014717.1 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:51022384 C>A maps to NM_001080457.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:51022384 C>A maps to NM_001080457.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:56300306 T>A maps to NM_145007.3 R907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:56300306 T>A maps to NM_145007.3 R907R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:58370974 C>T maps to NM_032828.2 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr19:58370974 C>T maps to NM_032828.2 Q399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:17998363 G>A maps to NM_001105569.1 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:17998363 G>A maps to NM_001105569.1 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:37235841 T>C maps to NM_019024.1 P1478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:37235841 T>C maps to NM_019024.1 P1478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:54137241 C>A maps to NM_014614.2 E848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:54137241 C>A maps to NM_014614.2 E848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:69043494 G>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:69043494 G>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:74867186 C>T maps to NM_138804.3 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:74867186 C>T maps to NM_138804.3 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:77745761 A>T maps to NM_001134745.1 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:77745761 A>T maps to NM_001134745.1 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:99155433 G>A maps to NM_001134224.1 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:99155433 G>A maps to NM_001134224.1 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:112942838 C>T maps to NM_153214.2 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:112942838 C>T maps to NM_153214.2 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:113316882 A>G maps to NM_019014.4 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:113316882 A>G maps to NM_019014.4 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:155566131 G>A maps to NM_002239.2 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:155566131 G>A maps to NM_002239.2 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:170028585 A>G maps to NM_004525.2 P3734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:170028585 A>G maps to NM_004525.2 P3734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:179419417 G>T maps to NM_133378.4 T26984T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:179419417 G>T maps to NM_133378.4 T26984T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:179442238 T>C did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:179442238 T>C did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:179490066 T>C maps to NM_133378.4 L12259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:179490066 T>C maps to NM_133378.4 L12259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:179578834 C>T maps to NM_133378.4 E7606E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:179578834 C>T maps to NM_133378.4 E7606E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:179617887 A>G maps to NM_133378.4 H3441H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:179617887 A>G maps to NM_133378.4 H3441H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:185801352 T>A maps to NM_194250.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:185801352 T>A maps to NM_194250.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:185803104 T>A maps to NM_194250.1 Y994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:185803104 T>A maps to NM_194250.1 Y994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:198263270 C>G maps to NM_012433.2 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:198263270 C>G maps to NM_012433.2 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:201846099 G>T maps to NM_173822.3 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:201846099 G>T maps to NM_173822.3 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:209302278 G>T maps to NM_005048.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:209302278 G>T maps to NM_005048.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:215301350 A>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:215301350 A>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:234862640 C>T maps to NM_024080.4 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:234862640 C>T maps to NM_024080.4 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:242648715 G>T maps to NM_032329.4 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr2:242648715 G>T maps to NM_032329.4 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr20:3675352 T>A maps to NM_023068.3 S967S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr20:3675352 T>A maps to NM_023068.3 S967S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr20:3677789 G>A maps to NM_023068.3 C774C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr20:3677789 G>A maps to NM_023068.3 C774C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr20:6021814 G>T maps to NM_152611.3 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr20:6021814 G>T maps to NM_152611.3 G692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr20:25057163 C>A maps to NM_014588.4 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr20:25057163 C>A maps to NM_014588.4 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr21:34878378 G>T maps to NM_001136006.1 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr21:34878378 G>T maps to NM_001136006.1 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr22:25601254 G>A maps to NM_004076.3 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr22:25601254 G>A maps to NM_004076.3 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr22:42383670 C>T maps to NM_145733.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr22:42383670 C>T maps to NM_145733.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:367720 T>A maps to NM_006614.2 C57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:367720 T>A maps to NM_006614.2 C57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:32932009 G>T maps to NM_001039111.1 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:32932009 G>T maps to NM_001039111.1 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:38793847 C>G maps to NM_006514.2 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:38793847 C>G maps to NM_006514.2 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:102196425 A>G maps to NM_175056.1 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:102196425 A>G maps to NM_175056.1 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:119236159 G>A maps to NM_016589.3 E235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:119236159 G>A maps to NM_016589.3 E235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:137802999 G>A maps to NM_173543.2 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:137802999 G>A maps to NM_173543.2 A386A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CV-7245-01A-11D-2012-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-CV-7245-01A-11D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:170789098 C>T maps to NM_015028.2 R1154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:170789098 C>T maps to NM_015028.2 R1154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:183855539 G>A maps to NM_003907.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr3:183855539 G>A maps to NM_003907.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:76415817 T>C maps to NM_015436.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:76415817 T>C maps to NM_015436.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:85657474 C>A maps to NM_014991.4 E2255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:85657474 C>A maps to NM_014991.4 E2255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:96222796 C>A maps to NM_003728.3 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:96222796 C>A maps to NM_003728.3 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:96469981 C>T maps to NM_003728.3 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:96469981 C>T maps to NM_003728.3 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:118975166 C>T maps to NM_004784.2 Y34Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:118975166 C>T maps to NM_004784.2 Y34Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:128726264 A>T maps to ENST00000438626 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:128726264 A>T maps to ENST00000438626 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:153565565 C>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:153565565 C>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:177649123 T>A did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:177649123 T>A did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:188924026 C>A maps to NM_174900.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr4:188924026 C>A maps to NM_174900.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:2752748 A>T maps to NM_178569.2 K72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:2752748 A>T maps to NM_178569.2 K72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:11236907 C>A maps to NM_001332.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:11236907 C>A maps to NM_001332.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:33684160 C>A did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:33684160 C>A did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:35641596 C>T maps to NM_024867.3 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:35641596 C>T maps to NM_024867.3 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:44815100 C>T maps to NM_016640.3 Q373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:44815100 C>T maps to NM_016640.3 Q373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:70835390 T>C maps to NM_018429.2 N1979N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:70835390 T>C maps to NM_018429.2 N1979N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:101709175 A>T maps to NM_173488.3 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:101709175 A>T maps to NM_173488.3 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:134029559 C>A maps to NM_021982.1 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:134029559 C>A maps to NM_021982.1 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:140180928 G>T maps to NM_018906.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:140180928 G>T maps to NM_018906.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:176675283 G>T maps to NM_022455.4 E1534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:176675283 G>T maps to NM_022455.4 E1534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:179192839 G>T maps to NM_014757.4 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr5:179192839 G>T maps to NM_014757.4 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:35425700 G>A maps to NM_021922.2 E303E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:35425700 G>A maps to NM_021922.2 E303E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:43013125 C>G maps to NM_001168370.1 T1043T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:43013125 C>G maps to NM_001168370.1 T1043T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:50803948 C>G maps to ENST00000263046 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:50803948 C>G maps to ENST00000263046 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:75843069 C>A maps to ENST00000322507 V1911V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:75843069 C>A maps to ENST00000322507 V1911V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:96651162 C>A maps to NM_006581.3 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:96651162 C>A maps to NM_006581.3 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:97562041 C>T maps to NM_052904.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:97562041 C>T maps to NM_052904.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:121562641 T>A maps to ENST00000275159 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:121562641 T>A maps to ENST00000275159 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:133836543 A>T maps to ENST00000452339 A535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:133836543 A>T maps to ENST00000452339 A535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:152443675 G>T maps to NM_182961.2 C8763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:152443675 G>T maps to NM_182961.2 C8763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:160557344 G>A maps to NM_003057.2 K311K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:160557344 G>A maps to NM_003057.2 K311K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:11676129 G>T maps to ENST00000423059 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:11676129 G>T maps to ENST00000423059 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:50514816 T>A maps to NM_022116.3 K57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:50514816 T>A maps to NM_022116.3 K57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:70853352 G>A maps to NM_022479.1 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:70853352 G>A maps to NM_022479.1 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:91631453 T>G maps to NM_005751.4 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:91631453 T>G maps to NM_005751.4 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:95668587 G>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:95668587 G>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:106508710 C>G maps to NM_002649.2 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:106508710 C>G maps to NM_002649.2 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:140482831 T>G maps to NM_004333.4 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:140482831 T>G maps to NM_004333.4 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:142640670 G>T maps to NM_000420.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:142640670 G>T maps to NM_000420.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:143175186 C>A maps to NM_176883.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr7:143175186 C>A maps to NM_176883.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:2044189 G>T maps to NM_003970.2 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:2044189 G>T maps to NM_003970.2 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:13356614 C>T maps to NM_182643.2 K322K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:13356614 C>T maps to NM_182643.2 K322K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:21965719 A>T maps to NM_024815.3 C100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:21965719 A>T maps to NM_024815.3 C100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:39682335 A>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:39682335 A>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:51449263 G>T maps to NM_018967.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:51449263 G>T maps to NM_018967.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:53045842 G>A maps to NM_014682.2 C773C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:53045842 G>A maps to NM_014682.2 C773C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:110509196 T>A maps to ENST00000426474 G3459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:110509196 T>A maps to ENST00000426474 G3459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:113694686 C>T maps to NM_198123.1 L887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:113694686 C>T maps to NM_198123.1 L887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:121290347 A>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:121290347 A>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:128753113 G>A maps to NM_002467.4 E425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:128753113 G>A maps to NM_002467.4 E425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:139824101 T>A maps to NM_152888.1 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr8:139824101 T>A maps to NM_152888.1 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr9:100070393 C>T maps to ENST00000375206 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr9:100070393 C>T maps to ENST00000375206 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr9:109687821 G>C maps to NM_021224.4 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr9:109687821 G>C maps to NM_021224.4 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr9:111735077 T>C maps to NM_003798.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr9:111735077 T>C maps to NM_003798.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr9:120476304 C>T maps to NM_138554.3 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr9:120476304 C>T maps to NM_138554.3 I633I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr9:136635536 C>A maps to NM_001134398.1 R770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr9:136635536 C>A maps to NM_001134398.1 R770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chrX:69502177 G>T maps to ENST00000374473 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chrX:69502177 G>T maps to ENST00000374473 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chrX:88009298 C>A maps to NM_033048.5 S295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chrX:88009298 C>A maps to NM_033048.5 S295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chrX:125299775 C>T maps to NM_001013628.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chrX:125299775 C>T maps to NM_001013628.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chrX:129149303 G>T maps to ENST00000303743 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chrX:129149303 G>T maps to ENST00000303743 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr1:25944780 C>T maps to NM_020379.2 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr1:25944780 C>T maps to NM_020379.2 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr1:57140141 A>C maps to NM_006252.3 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr1:57140141 A>C maps to NM_006252.3 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr1:161140305 G>A maps to NM_001122764.1 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr1:161140305 G>A maps to NM_001122764.1 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr1:236760192 T>C maps to NM_018072.5 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr1:236760192 T>C maps to NM_018072.5 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr1:247978413 G>A maps to NM_001001966.1 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr1:247978413 G>A maps to NM_001001966.1 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr10:93602104 C>T maps to NM_025235.3 C672C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr10:93602104 C>T maps to NM_025235.3 C672C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr11:8414254 A>C maps to NM_030906.2 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr11:8414254 A>C maps to NM_030906.2 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr11:55433283 G>A maps to NM_001004704.1 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr11:55433283 G>A maps to NM_001004704.1 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr15:79750589 A>T maps to NM_015206.2 K701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr15:79750589 A>T maps to NM_015206.2 K701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr16:2159542 G>C maps to NM_001009944.2 V1875V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr16:2159542 G>C maps to NM_001009944.2 V1875V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr16:30779807 C>A maps to NM_014771.2 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr16:30779807 C>A maps to NM_014771.2 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr17:63526138 C>T maps to NM_004655.3 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr17:63526138 C>T maps to NM_004655.3 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr19:19655255 G>A maps to NM_153221.2 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr19:19655255 G>A maps to NM_153221.2 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr19:51135983 A>T maps to NM_001160329.1 L78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr19:51135983 A>T maps to NM_001160329.1 L78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr2:135965228 C>T maps to NM_032143.2 A928A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr2:135965228 C>T maps to NM_032143.2 A928A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr22:41919935 G>A maps to ENST00000396512 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr22:41919935 G>A maps to ENST00000396512 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr3:113378749 G>C maps to NM_001009899.2 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr3:113378749 G>C maps to NM_001009899.2 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr6:80878707 G>A maps to NM_183050.2 Q198Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr6:80878707 G>A maps to NM_183050.2 Q198Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr7:11468651 C>G maps to ENST00000423059 V1055V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr7:11468651 C>G maps to ENST00000423059 V1055V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr9:95236913 G>C maps to NM_017680.4 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr9:95236913 G>C maps to NM_017680.4 S89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chrX:48629491 C>T maps to NM_001080489.2 H117H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chrX:48629491 C>T maps to NM_001080489.2 H117H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:13183461 A>G maps to NM_001136561.2 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:13183461 A>G maps to NM_001136561.2 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:20246800 C>T maps to NM_014589.1 *143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:20246800 C>T maps to NM_014589.1 *143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:74507087 G>T maps to NM_001105659.1 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:74507087 G>T maps to NM_001105659.1 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:86289269 G>T maps to NM_152890.5 G1246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:86289269 G>T maps to NM_152890.5 G1246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:111217038 G>T maps to NM_002232.3 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:111217038 G>T maps to NM_002232.3 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:150529139 G>A maps to ENST00000369039 W563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:150529139 G>A maps to ENST00000369039 W563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:152191467 G>T maps to NM_001009931.1 G879G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:152191467 G>T maps to NM_001009931.1 G879G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:158583632 C>G maps to NM_003126.2 G2289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:158583632 C>G maps to NM_003126.2 G2289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:183387390 G>C maps to NM_015039.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:183387390 G>C maps to NM_015039.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:197898130 G>C did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:197898130 G>C did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr10:129906869 T>A maps to NM_002417.4 P1078P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr10:129906869 T>A maps to NM_002417.4 P1078P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:16847839 C>T maps to ENST00000448080 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:16847839 C>T maps to ENST00000448080 R390R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:55432836 C>A maps to NM_001004704.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:55432836 C>A maps to NM_001004704.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:55595554 C>A maps to NM_001004739.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:55595554 C>A maps to NM_001004739.1 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:57175324 G>A maps to ENST00000428603 H485H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:57175324 G>A maps to ENST00000428603 H485H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:65623194 G>T maps to NM_005507.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:65623194 G>T maps to NM_005507.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:65634508 C>A maps to NM_016938.3 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:65634508 C>A maps to NM_016938.3 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:82644764 T>A maps to NM_145018.3 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:82644764 T>A maps to NM_145018.3 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:130319056 C>T maps to NM_139055.2 D63D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr11:130319056 C>T maps to NM_139055.2 D63D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr12:6729715 C>T maps to ENST00000435659 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr12:6729715 C>T maps to ENST00000435659 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr12:11546522 G>T maps to NM_006248.3 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr12:11546522 G>T maps to NM_006248.3 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr12:49424104 T>A maps to NM_003482.3 K4653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr12:49424104 T>A maps to NM_003482.3 K4653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr12:50367219 C>T maps to NM_001652.3 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr12:50367219 C>T maps to NM_001652.3 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr13:53036053 G>T maps to NM_001098525.1 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr13:53036053 G>T maps to NM_001098525.1 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr13:109707434 G>A maps to NM_015011.1 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr13:109707434 G>A maps to NM_015011.1 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr14:59112195 T>C maps to NM_016651.5 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr14:59112195 T>C maps to NM_016651.5 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr14:62547850 T>C maps to NM_031914.2 C431C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr14:62547850 T>C maps to NM_031914.2 C431C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr14:101349301 G>T maps to NM_001134888.2 Y608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr14:101349301 G>T maps to NM_001134888.2 Y608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr15:53050033 C>T maps to NM_004498.1 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr15:53050033 C>T maps to NM_004498.1 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr15:54847644 G>T maps to ENST00000260323 E1965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr15:54847644 G>T maps to ENST00000260323 E1965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr15:55657498 G>A maps to ENST00000442196 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr15:55657498 G>A maps to ENST00000442196 Q239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr16:81236233 G>A maps to NM_052892.3 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr16:81236233 G>A maps to NM_052892.3 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr17:8926248 C>A maps to NM_004822.2 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr17:8926248 C>A maps to NM_004822.2 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr17:31439076 T>C maps to NM_183377.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr17:31439076 T>C maps to NM_183377.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr17:35298159 C>A maps to NM_005568.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr17:35298159 C>A maps to NM_005568.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr17:45219296 T>G maps to NM_001114091.1 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr17:45219296 T>G maps to NM_001114091.1 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr18:7949202 C>T maps to NM_001105244.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr18:7949202 C>T maps to NM_001105244.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr18:64178850 A>T maps to NM_021153.2 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr18:64178850 A>T maps to NM_021153.2 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr18:64202256 A>T maps to NM_021153.2 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr18:64202256 A>T maps to NM_021153.2 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr19:7506610 G>T maps to NM_001130955.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr19:7506610 G>T maps to NM_001130955.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr19:39390155 T>C maps to NM_012237.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr19:39390155 T>C maps to NM_012237.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr19:43439856 T>C maps to NM_002783.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr19:43439856 T>C maps to NM_002783.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr19:48337741 C>T maps to NM_000554.4 N14N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr19:48337741 C>T maps to NM_000554.4 N14N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr19:48785740 C>T maps to NM_153608.1 N41N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr19:48785740 C>T maps to NM_153608.1 N41N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr19:51133411 G>A maps to NM_001160329.1 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr19:51133411 G>A maps to NM_001160329.1 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:24484539 T>A maps to NM_006277.2 P809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:24484539 T>A maps to NM_006277.2 P809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:26687857 G>A maps to NM_194248.2 S1613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:26687857 G>A maps to NM_194248.2 S1613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:31483476 G>T maps to NM_014600.2 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:31483476 G>T maps to NM_014600.2 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:79255020 T>A maps to NM_001008387.1 L141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:79255020 T>A maps to NM_001008387.1 L141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:88991473 C>T maps to NM_144563.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:88991473 C>T maps to NM_144563.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:128937401 G>C maps to NM_020120.3 V1286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:128937401 G>C maps to NM_020120.3 V1286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:179423145 G>T maps to NM_133378.4 R26446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:179423145 G>T maps to NM_133378.4 R26446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:185803440 C>T maps to NM_194250.1 H1106H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:185803440 C>T maps to NM_194250.1 H1106H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:190718962 A>G did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:190718962 A>G did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr20:21346225 A>T maps to NM_012255.3 V780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr20:21346225 A>T maps to NM_012255.3 V780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr22:32479070 G>A maps to NM_000343.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr22:32479070 G>A maps to NM_000343.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr3:13670761 C>T maps to NM_001165035.1 Q938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr3:13670761 C>T maps to NM_001165035.1 Q938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr3:89480487 A>T maps to NM_005233.5 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr3:89480487 A>T maps to NM_005233.5 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr3:109031509 C>T maps to NM_138815.3 E21E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr3:109031509 C>T maps to NM_138815.3 E21E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr4:71096931 G>A maps to NM_152997.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr4:71096931 G>A maps to NM_152997.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr4:85414621 C>G maps to NM_006168.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr4:85414621 C>G maps to NM_006168.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr4:113356373 G>T maps to NM_025144.3 G1035G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr4:113356373 G>T maps to NM_025144.3 G1035G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr4:155249331 G>A maps to NM_017639.3 Q856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr4:155249331 G>A maps to NM_017639.3 Q856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr4:166916210 A>G did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr4:166916210 A>G did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr5:38486029 C>T maps to NM_002310.5 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr5:38486029 C>T maps to NM_002310.5 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr5:128958004 T>C maps to NM_133638.3 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr5:128958004 T>C maps to NM_133638.3 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr5:129070696 G>T maps to NM_133638.3 G1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr5:129070696 G>T maps to NM_133638.3 G1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr5:140720340 C>T maps to NM_018915.2 N601N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr5:140720340 C>T maps to NM_018915.2 N601N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr5:145838778 A>G maps to NM_006706.3 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr5:145838778 A>G maps to NM_006706.3 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr6:348138 C>T maps to ENST00000457386 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr6:348138 C>T maps to ENST00000457386 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr6:62604605 C>A maps to NM_152688.2 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr6:62604605 C>A maps to NM_152688.2 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr6:69349245 G>T maps to NM_001704.2 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr6:69349245 G>T maps to NM_001704.2 E227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr6:152674535 C>T maps to NM_182961.2 Q3705Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr6:152674535 C>T maps to NM_182961.2 Q3705Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr6:167708042 G>T maps to NM_018974.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr6:167708042 G>T maps to NM_018974.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr7:26236078 T>G maps to NM_031243.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr7:26236078 T>G maps to NM_031243.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr7:86468528 G>T maps to NM_000840.2 E567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr7:86468528 G>T maps to NM_000840.2 E567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr7:100281722 C>G maps to NM_022574.4 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr7:100281722 C>G maps to NM_022574.4 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr7:102952104 A>T maps to NM_004279.2 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr7:102952104 A>T maps to NM_004279.2 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr7:127253103 C>T maps to NM_006193.2 E221E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr7:127253103 C>T maps to NM_006193.2 E221E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr7:147259326 G>T maps to NM_014141.5 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr7:147259326 G>T maps to NM_014141.5 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr8:12583337 A>T maps to NM_152271.3 V687V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr8:12583337 A>T maps to NM_152271.3 V687V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr8:41552253 C>T maps to ENST00000415018 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr8:41552253 C>T maps to ENST00000415018 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr9:131001791 C>T maps to ENST00000372923 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr9:131001791 C>T maps to ENST00000372923 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr9:134503938 C>T maps to NM_198679.1 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr9:134503938 C>T maps to NM_198679.1 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr9:140611504 G>A maps to NM_024757.4 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr9:140611504 G>A maps to NM_024757.4 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:18919704 G>T maps to NM_000292.2 S975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:18919704 G>T maps to NM_000292.2 S975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:30327462 G>A maps to NM_000475.4 H6H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:30327462 G>A maps to NM_000475.4 H6H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:47836066 G>C maps to NM_006962.1 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:47836066 G>C maps to NM_006962.1 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:48418231 G>A maps to NM_002536.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:48418231 G>A maps to NM_002536.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:55513446 A>T maps to NM_201286.3 C642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:55513446 A>T maps to NM_201286.3 C642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:72667340 C>T maps to NM_005193.1 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:72667340 C>T maps to NM_005193.1 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:74494241 C>A maps to NM_145052.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:74494241 C>A maps to NM_145052.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:106200164 C>G did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:106200164 C>G did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:109695143 C>G maps to NM_020769.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:109695143 C>G maps to NM_020769.2 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:115593059 G>T maps to NM_001017978.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:115593059 G>T maps to NM_001017978.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:119694441 G>A maps to NM_003588.3 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:119694441 G>A maps to NM_003588.3 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:123181322 A>C maps to NM_001042750.1 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:123181322 A>C maps to NM_001042750.1 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:127185944 C>A maps to NM_138289.3 G81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:127185944 C>A maps to NM_138289.3 G81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:135288650 G>C maps to NM_001159699.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:135288650 G>C maps to NM_001159699.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:135482270 T>A maps to NM_153834.3 G2857G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:135482270 T>A maps to NM_153834.3 G2857G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:139866429 C>T maps to NM_004065.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:139866429 C>T maps to NM_004065.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:153049746 A>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:153049746 A>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:153218075 C>A maps to ENST00000369984 E1655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chrX:153218075 C>A maps to ENST00000369984 E1655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:97278596 G>A maps to ENST00000421845 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr2:97278596 G>A maps to ENST00000421845 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr7:101813748 G>A maps to ENST00000360264 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr7:101813748 G>A maps to ENST00000360264 E260E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:57422502 A>G maps to NM_000066.2 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:57422502 A>G maps to NM_000066.2 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:94669494 A>G maps to NM_004815.3 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:94669494 A>G maps to NM_004815.3 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:150941484 G>A maps to NM_181746.2 R28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:150941484 G>A maps to NM_181746.2 R28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:202287593 G>A maps to NM_001017403.1 A721A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:202287593 G>A maps to NM_001017403.1 A721A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:203008175 C>T maps to ENST00000367238 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:203008175 C>T maps to ENST00000367238 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:205238350 C>T maps to NM_014858.3 Q341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:205238350 C>T maps to NM_014858.3 Q341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:235904811 G>A maps to NM_000081.2 H2756H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:235904811 G>A maps to NM_000081.2 H2756H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:236714246 C>T maps to NM_018072.5 Q2130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr1:236714246 C>T maps to NM_018072.5 Q2130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr10:45484753 G>A maps to NM_032023.3 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr10:45484753 G>A maps to NM_032023.3 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr10:69925474 G>A maps to NM_032578.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr10:69925474 G>A maps to NM_032578.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr10:103291077 A>T maps to NM_033637.2 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr10:103291077 A>T maps to NM_033637.2 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr10:103343336 G>A maps to NM_013274.3 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr10:103343336 G>A maps to NM_013274.3 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr11:720676 G>A maps to NM_022772.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr11:720676 G>A maps to NM_022772.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr11:115102136 G>A maps to NM_014333.3 C166C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr11:115102136 G>A maps to NM_014333.3 C166C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr11:122852271 C>T maps to NM_001098169.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr11:122852271 C>T maps to NM_001098169.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr12:666882 G>A maps to NM_173593.3 E830E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr12:666882 G>A maps to NM_173593.3 E830E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr12:29469873 G>A maps to NM_018099.3 W352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr12:29469873 G>A maps to NM_018099.3 W352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr12:54396247 C>A maps to NM_006897.1 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr12:54396247 C>A maps to NM_006897.1 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr13:21331599 C>T maps to NM_174928.1 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr13:21331599 C>T maps to NM_174928.1 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr13:33703124 A>G maps to NM_178007.2 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr13:33703124 A>G maps to NM_178007.2 P555P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr14:70633783 C>A maps to NM_183002.1 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr14:70633783 C>A maps to NM_183002.1 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr14:88940130 G>A maps to NM_007039.3 R843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr14:88940130 G>A maps to NM_007039.3 R843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr14:102900896 G>T maps to NM_014844.3 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr14:102900896 G>T maps to NM_014844.3 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr15:25213156 C>T maps to NM_022804.2 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr15:25213156 C>T maps to NM_022804.2 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr15:25959361 G>T maps to NM_024490.3 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr15:25959361 G>T maps to NM_024490.3 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr15:50788055 G>C maps to NM_005154.3 R890R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr15:50788055 G>C maps to NM_005154.3 R890R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr17:46239900 C>T maps to NM_003726.3 W303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr17:46239900 C>T maps to NM_003726.3 W303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr17:46620657 C>T maps to NM_002145.3 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr17:46620657 C>T maps to NM_002145.3 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr17:72233623 C>T maps to NM_032646.5 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr17:72233623 C>T maps to NM_032646.5 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr17:72285735 C>T maps to NM_023036.4 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr17:72285735 C>T maps to NM_023036.4 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr18:14797797 A>G maps to NM_001145029.1 K658K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr18:14797797 A>G maps to NM_001145029.1 K658K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr19:20308130 T>C maps to ENST00000428290 D198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr19:20308130 T>C maps to ENST00000428290 D198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr19:51633225 G>T maps to NM_014441.2 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr19:51633225 G>T maps to NM_014441.2 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr19:53058289 C>T maps to NM_001039886.3 Y707Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr19:53058289 C>T maps to NM_001039886.3 Y707Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr19:53762611 C>T maps to NM_173856.2 Y328Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr19:53762611 C>T maps to NM_173856.2 Y328Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr2:25468196 G>A maps to NM_175629.1 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr2:25468196 G>A maps to NM_175629.1 I493I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr2:108488440 A>G maps to NM_182588.2 E1327E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr2:108488440 A>G maps to NM_182588.2 E1327E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr2:119603945 C>T maps to NM_001426.3 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr2:119603945 C>T maps to NM_001426.3 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr2:152423804 G>A maps to NM_001164507.1 A6011A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr2:152423804 G>A maps to NM_001164507.1 A6011A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr20:9561115 G>A maps to NM_177990.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr20:9561115 G>A maps to NM_177990.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr20:34078579 C>T maps to NM_007186.3 Q902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr20:34078579 C>T maps to NM_007186.3 Q902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr20:36869728 G>A maps to NM_001029864.1 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr20:36869728 G>A maps to NM_001029864.1 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr22:25131808 G>A maps to NM_001008496.2 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr22:25131808 G>A maps to NM_001008496.2 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr3:37033929 G>A maps to NM_014805.3 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr3:37033929 G>A maps to NM_014805.3 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr3:41267195 C>T maps to NM_001904.3 H260H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr3:41267195 C>T maps to NM_001904.3 H260H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr3:45127377 G>A maps to NM_022842.3 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr3:45127377 G>A maps to NM_022842.3 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr3:52637657 A>G maps to ENST00000296302 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr3:52637657 A>G maps to ENST00000296302 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr3:101535733 C>T maps to NM_145037.2 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr3:101535733 C>T maps to NM_145037.2 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr3:129303020 G>A maps to NM_015103.2 A695A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr3:129303020 G>A maps to NM_015103.2 A695A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr4:70620402 C>A maps to NM_014465.3 G88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr4:70620402 C>A maps to NM_014465.3 G88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr4:140309171 G>A maps to NM_057175.3 E845E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr4:140309171 G>A maps to NM_057175.3 E845E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr4:183601502 G>A did not map to a codon.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr4:183601502 G>A did not map to a codon.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr4:187557354 G>C maps to ENST00000260147 S1336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr4:187557354 G>C maps to ENST00000260147 S1336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr5:96478235 G>A maps to NM_153234.4 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr5:96478235 G>A maps to NM_153234.4 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr5:114588909 C>T maps to NM_005023.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr5:114588909 C>T maps to NM_005023.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr5:140202652 G>A maps to NM_018908.2 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr5:140202652 G>A maps to NM_018908.2 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr5:161128535 G>A maps to NM_000811.2 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr5:161128535 G>A maps to NM_000811.2 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr5:176665391 C>A maps to NM_022455.4 S1359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr5:176665391 C>A maps to NM_022455.4 S1359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr6:31084821 G>T maps to NM_001264.4 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr6:31084821 G>T maps to NM_001264.4 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr6:54245332 A>T maps to NM_014464.3 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr6:54245332 A>T maps to NM_014464.3 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr6:70428851 G>C maps to NM_018368.3 S253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr6:70428851 G>C maps to NM_018368.3 S253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr6:90384309 T>C did not map to a codon.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr6:90384309 T>C did not map to a codon.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr6:161159605 C>T maps to NM_000301.3 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr6:161159605 C>T maps to NM_000301.3 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr7:4185402 C>A maps to NM_152744.3 T1426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr7:4185402 C>A maps to NM_152744.3 T1426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr7:95039307 G>A maps to NM_000305.2 H200H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr7:95039307 G>A maps to NM_000305.2 H200H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr7:112407740 G>C maps to NM_022484.4 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr7:112407740 G>C maps to NM_022484.4 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr7:158449249 C>T maps to NM_017760.5 Q736Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr7:158449249 C>T maps to NM_017760.5 Q736Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr8:17611495 G>C maps to NM_001001924.2 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr8:17611495 G>C maps to NM_001001924.2 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr8:75227562 G>C maps to NM_020647.2 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr8:75227562 G>C maps to NM_020647.2 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr8:113326781 A>T maps to NM_198123.1 P2475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr8:113326781 A>T maps to NM_198123.1 P2475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr8:144808543 G>A maps to NM_198488.3 N1029N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr8:144808543 G>A maps to NM_198488.3 N1029N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr8:145060328 C>T maps to NM_032789.3 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr8:145060328 C>T maps to NM_032789.3 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr8:145746351 G>A maps to NM_014665.2 E324E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr8:145746351 G>A maps to NM_014665.2 E324E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr9:27218814 G>T maps to NM_000459.3 G1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr9:27218814 G>T maps to NM_000459.3 G1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr9:36170743 C>T maps to NM_005893.2 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr9:36170743 C>T maps to NM_005893.2 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr9:104449191 G>A maps to NM_133445.2 C330C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr9:104449191 G>A maps to NM_133445.2 C330C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr9:135204920 G>A maps to ENST00000372169 C688C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr9:135204920 G>A maps to ENST00000372169 C688C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr9:136234222 G>A maps to NM_033161.2 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr9:136234222 G>A maps to NM_033161.2 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr9:137809627 C>T maps to NM_002003.3 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr9:137809627 C>T maps to NM_002003.3 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chrX:41390288 G>A maps to ENST00000378163 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chrX:41390288 G>A maps to ENST00000378163 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:11579444 G>T maps to NM_020780.1 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:11579444 G>T maps to NM_020780.1 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:16456828 C>T maps to NM_004431.3 W854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:16456828 C>T maps to NM_004431.3 W854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:22816680 G>A maps to NM_014870.3 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:22816680 G>A maps to NM_014870.3 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:57209832 C>T maps to NM_001004303.4 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:57209832 C>T maps to NM_001004303.4 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:62960062 T>C maps to ENST00000371140 E1700E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:62960062 T>C maps to ENST00000371140 E1700E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:109812162 G>A maps to NM_001408.2 E2310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:109812162 G>A maps to NM_001408.2 E2310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:156756530 G>A maps to NM_005973.4 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:156756530 G>A maps to NM_005973.4 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:160769733 C>T maps to ENST00000263285 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:160769733 C>T maps to ENST00000263285 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:200842299 C>G maps to NM_005298.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:200842299 C>G maps to NM_005298.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:205631060 G>A maps to NM_033102.2 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:205631060 G>A maps to NM_033102.2 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:228468381 C>T maps to NM_001098623.1 F2694F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:228468381 C>T maps to NM_001098623.1 F2694F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:233489591 C>T maps to NM_032435.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr1:233489591 C>T maps to NM_032435.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr10:26377302 C>T maps to NM_017433.4 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr10:26377302 C>T maps to NM_017433.4 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr10:73537540 C>T maps to ENST00000398860 L1655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr10:73537540 C>T maps to ENST00000398860 L1655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr10:94828252 G>A maps to NM_183374.2 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr10:94828252 G>A maps to NM_183374.2 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr11:205337 G>A maps to NM_001098787.1 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr11:205337 G>A maps to NM_001098787.1 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr11:8478906 T>A maps to NM_030906.2 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr11:8478906 T>A maps to NM_030906.2 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr11:61084031 C>T maps to NM_001923.3 W411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr11:61084031 C>T maps to NM_001923.3 W411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr11:65788060 G>A maps to NM_053054.3 I655I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr11:65788060 G>A maps to NM_053054.3 I655I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:11422582 C>T maps to NM_006249.4 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:11422582 C>T maps to NM_006249.4 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:12318021 G>A maps to NM_002336.2 R585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:12318021 G>A maps to NM_002336.2 R585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:31605305 A>T maps to NM_144973.3 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:31605305 A>T maps to NM_144973.3 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:43777494 G>A maps to ENST00000389420 R1555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:43777494 G>A maps to ENST00000389420 R1555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:46245638 C>T maps to NM_152641.2 Q1245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:46245638 C>T maps to NM_152641.2 Q1245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:54367366 C>A maps to NM_014212.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:54367366 C>A maps to NM_014212.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:63964554 G>T maps to NM_173812.4 Y661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:63964554 G>T maps to NM_173812.4 Y661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:72005624 C>G maps to NM_144982.4 L1890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:72005624 C>G maps to NM_144982.4 L1890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:121947474 C>T maps to ENST00000377071 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:121947474 C>T maps to ENST00000377071 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:132326313 C>T maps to NM_016155.4 Y284Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr12:132326313 C>T maps to NM_016155.4 Y284Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr14:24566130 C>A maps to NM_004563.2 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr14:24566130 C>A maps to NM_004563.2 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr14:35872922 G>A maps to NM_020529.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr14:35872922 G>A maps to NM_020529.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr14:70634139 G>A maps to NM_183002.1 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr14:70634139 G>A maps to NM_183002.1 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr14:95035799 G>A maps to NM_006215.2 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr14:95035799 G>A maps to NM_006215.2 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr14:104142024 G>A did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr14:104142024 G>A did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr15:34649145 G>A maps to ENST00000438749 E969E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr15:34649145 G>A maps to ENST00000438749 E969E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr15:101447333 G>T maps to NM_000693.2 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr15:101447333 G>T maps to NM_000693.2 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr15:101448627 C>T maps to NM_000693.2 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr15:101448627 C>T maps to NM_000693.2 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr16:732455 C>T maps to NM_005861.2 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr16:732455 C>T maps to NM_005861.2 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr16:21181822 C>T maps to ENST00000451578 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr16:21181822 C>T maps to ENST00000451578 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr16:21262062 G>A maps to NM_145865.2 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr16:21262062 G>A maps to NM_145865.2 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr16:51171358 G>A maps to ENST00000251020 F1213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr16:51171358 G>A maps to ENST00000251020 F1213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr16:68721544 C>T maps to NM_001793.4 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr16:68721544 C>T maps to NM_001793.4 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr17:961285 C>T did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr17:961285 C>T did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr17:1704087 T>C maps to NM_052928.2 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr17:1704087 T>C maps to NM_052928.2 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr17:6665480 A>G maps to NM_017523.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr17:6665480 A>G maps to NM_017523.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr17:7579532 G>A maps to NM_001126112.1 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr17:7579532 G>A maps to NM_001126112.1 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr17:37761718 C>A maps to NM_006160.3 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr17:37761718 C>A maps to NM_006160.3 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr18:54423843 C>T maps to NM_015285.2 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr18:54423843 C>T maps to NM_015285.2 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:4037461 G>A maps to NM_015897.2 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:4037461 G>A maps to NM_015897.2 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:12491593 G>A did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:12491593 G>A did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:13928081 G>A maps to NM_023072.2 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:13928081 G>A maps to NM_023072.2 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:36228843 G>C did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:36228843 G>C did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:40368525 G>A maps to NM_003890.2 Y4274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:40368525 G>A maps to NM_003890.2 Y4274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:40704315 C>T maps to NM_002446.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:40704315 C>T maps to NM_002446.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:50374956 C>T maps to ENST00000391835 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:50374956 C>T maps to ENST00000391835 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:51192463 C>T maps to ENST00000391814 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr19:51192463 C>T maps to ENST00000391814 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr2:31805804 G>T maps to NM_000348.3 C55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr2:31805804 G>T maps to NM_000348.3 C55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr2:160832578 C>T maps to NM_007366.4 A865A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr2:160832578 C>T maps to NM_007366.4 A865A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr2:234354352 C>T maps to NM_152879.2 Q427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr2:234354352 C>T maps to NM_152879.2 Q427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr20:44515634 G>A maps to NM_080608.3 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr20:44515634 G>A maps to NM_080608.3 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr21:30318478 G>A maps to NM_015565.2 F1252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr21:30318478 G>A maps to NM_015565.2 F1252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr21:34011424 G>A maps to NM_003895.3 F1275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr21:34011424 G>A maps to NM_003895.3 F1275F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr3:30713558 C>G maps to NM_001024847.2 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr3:30713558 C>G maps to NM_001024847.2 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr5:76645308 C>T maps to NM_003719.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr5:76645308 C>T maps to NM_003719.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr5:141335105 G>A maps to NM_016580.2 Q771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr5:141335105 G>A maps to NM_016580.2 Q771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr5:154214194 G>A maps to NM_032385.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr5:154214194 G>A maps to NM_032385.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr5:169805749 C>T maps to NM_004137.2 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr5:169805749 C>T maps to NM_004137.2 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr6:34496435 C>T maps to NM_020804.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr6:34496435 C>T maps to NM_020804.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr6:46108042 C>T maps to NM_014936.4 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr6:46108042 C>T maps to NM_014936.4 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr6:51921547 G>A maps to NM_138694.3 C547C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr6:51921547 G>A maps to NM_138694.3 C547C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr6:110567451 G>A maps to NM_001123364.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr6:110567451 G>A maps to NM_001123364.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr6:111693796 A>G did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr6:111693796 A>G did not map to a codon.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr6:123332246 C>T maps to NM_001010852.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr6:123332246 C>T maps to NM_001010852.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr6:168434600 C>T maps to NM_030615.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr6:168434600 C>T maps to NM_030615.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr7:97617810 G>A maps to NM_006188.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr7:97617810 G>A maps to NM_006188.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr7:100276154 C>T maps to NM_005273.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr7:100276154 C>T maps to NM_005273.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr7:100280032 C>T maps to NM_022574.4 L891L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr7:100280032 C>T maps to NM_022574.4 L891L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr7:117375086 G>A maps to NM_033427.2 A1252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr7:117375086 G>A maps to NM_033427.2 A1252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr7:127669961 G>C maps to NM_022143.4 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr7:127669961 G>C maps to NM_022143.4 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr7:127670192 G>A maps to NM_022143.4 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr7:127670192 G>A maps to NM_022143.4 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr7:148112632 G>A maps to NM_014141.5 A1307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr7:148112632 G>A maps to NM_014141.5 A1307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr8:6794388 G>T maps to NM_001925.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr8:6794388 G>T maps to NM_001925.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr8:19231061 A>G maps to NM_022071.3 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr8:19231061 A>G maps to NM_022071.3 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr8:27289832 G>A maps to NM_004103.3 E314E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr8:27289832 G>A maps to NM_004103.3 E314E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr8:37623260 C>A maps to NM_007198.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr8:37623260 C>A maps to NM_007198.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr8:99039680 C>T maps to ENST00000254898 I660I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr8:99039680 C>T maps to ENST00000254898 I660I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr8:121267541 G>A maps to NM_021110.1 W939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr8:121267541 G>A maps to NM_021110.1 W939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr8:143746148 C>T maps to NM_003724.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr8:143746148 C>T maps to NM_003724.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr9:126136902 C>T maps to NM_173689.5 L1145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr9:126136902 C>T maps to NM_173689.5 L1145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr9:133932454 G>A maps to ENST00000355048 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr9:133932454 G>A maps to ENST00000355048 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chrX:17744772 G>A maps to NM_198270.2 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chrX:17744772 G>A maps to NM_198270.2 P828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chrX:38009041 G>A maps to NM_006307.4 F439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chrX:38009041 G>A maps to NM_006307.4 F439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chrX:43652759 C>A maps to NM_000898.4 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chrX:43652759 C>A maps to NM_000898.4 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chrX:69458110 C>A maps to NM_001013579.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chrX:69458110 C>A maps to NM_001013579.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chrX:154292276 G>A maps to NM_001018024.2 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chrX:154292276 G>A maps to NM_001018024.2 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr17:39324346 G>T maps to NM_033187.1 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7252-01A-11D-2012-08 chr17:39324346 G>T maps to NM_033187.1 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr1:147091475 C>T maps to NM_004326.2 H505H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr1:147091475 C>T maps to NM_004326.2 H505H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr1:153745727 G>A maps to ENST00000428986 V1038V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr1:153745727 G>A maps to ENST00000428986 V1038V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr1:165737483 G>A maps to NM_019026.3 Y31Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr1:165737483 G>A maps to NM_019026.3 Y31Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr1:186645173 A>C maps to NM_000963.2 Y371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr1:186645173 A>C maps to NM_000963.2 Y371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr1:233397850 A>G maps to NM_014801.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr1:233397850 A>G maps to NM_014801.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr1:241032089 T>A maps to ENST00000407727 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr1:241032089 T>A maps to ENST00000407727 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr10:102247815 C>A maps to NM_015490.3 E1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr10:102247815 C>A maps to NM_015490.3 E1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr11:67412540 C>T maps to NM_080658.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr11:67412540 C>T maps to NM_080658.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr12:2760858 C>A maps to NM_199460.2 V1381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr12:2760858 C>A maps to NM_199460.2 V1381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr12:53878058 C>T maps to NM_001193511.1 E410E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr12:53878058 C>T maps to NM_001193511.1 E410E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr12:121013685 C>T maps to ENST00000458409 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr12:121013685 C>T maps to ENST00000458409 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr12:122181638 G>A maps to NM_001080825.2 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr12:122181638 G>A maps to NM_001080825.2 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr13:27649389 T>C maps to NM_182488.3 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr13:27649389 T>C maps to NM_182488.3 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr13:38160348 G>T maps to NM_006475.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr13:38160348 G>T maps to NM_006475.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr13:39588613 C>G did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr13:39588613 C>G did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr13:41891056 G>T maps to NM_024561.4 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr13:41891056 G>T maps to NM_024561.4 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr13:115002174 G>T did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr13:115002174 G>T did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr15:78894290 G>T maps to NM_000743.4 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr15:78894290 G>T maps to NM_000743.4 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr16:3722788 C>T maps to NM_016292.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr16:3722788 C>T maps to NM_016292.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr16:57994741 A>G did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr16:57994741 A>G did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr16:58572082 C>T maps to NM_016284.3 Q1741Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr16:58572082 C>T maps to NM_016284.3 Q1741Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr16:65038543 C>A did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr16:65038543 C>A did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr17:1945364 G>A maps to NM_080822.2 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr17:1945364 G>A maps to NM_080822.2 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr17:3977537 A>G maps to NM_015113.3 D1197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr17:3977537 A>G maps to NM_015113.3 D1197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr17:5009728 G>T maps to NM_014519.2 S242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr17:5009728 G>T maps to NM_014519.2 S242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr17:18075504 C>T maps to ENST00000205890 S3417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr17:18075504 C>T maps to ENST00000205890 S3417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr18:44424057 C>A maps to NM_004671.2 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr18:44424057 C>A maps to NM_004671.2 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr19:16034705 G>A maps to NM_021187.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr19:16034705 G>A maps to NM_021187.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr19:36853053 C>T maps to NM_020917.2 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr19:36853053 C>T maps to NM_020917.2 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr19:40886276 G>A maps to NM_144685.3 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr19:40886276 G>A maps to NM_144685.3 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr19:50046457 C>T maps to NM_020650.2 H325H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr19:50046457 C>T maps to NM_020650.2 H325H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr19:56539845 C>T maps to NM_153447.4 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr19:56539845 C>T maps to NM_153447.4 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:20138032 G>A maps to NM_001006657.1 R697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:20138032 G>A maps to NM_001006657.1 R697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:56419697 G>A maps to NM_001080433.1 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:56419697 G>A maps to NM_001080433.1 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:68772423 C>G maps to NM_173545.2 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:68772423 C>G maps to NM_173545.2 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:86075250 A>T maps to NM_003896.3 L132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:86075250 A>T maps to NM_003896.3 L132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:128394184 C>T maps to ENST00000389524 L2038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:128394184 C>T maps to ENST00000389524 L2038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:131521972 G>A maps to NM_001105195.1 Q776Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:131521972 G>A maps to NM_001105195.1 Q776Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:160028630 G>T did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:160028630 G>T did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:179604399 A>G maps to NM_133437.3 T4349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:179604399 A>G maps to NM_133437.3 T4349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:207509208 G>A maps to NM_001102659.1 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:207509208 G>A maps to NM_001102659.1 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:220424010 C>T maps to NM_015311.2 E1054E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:220424010 C>T maps to NM_015311.2 E1054E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:241657474 C>T maps to ENST00000373308 G1783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr2:241657474 C>T maps to ENST00000373308 G1783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr20:9391724 G>T maps to NM_001172646.1 G681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr20:9391724 G>T maps to NM_001172646.1 G681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr20:56189964 T>C maps to NM_030776.2 K160K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr20:56189964 T>C maps to NM_030776.2 K160K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr21:31744003 T>A maps to NM_181621.3 *176C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr21:31744003 T>A maps to NM_181621.3 *176C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr3:194081061 G>A maps to NM_001135057.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr3:194081061 G>A maps to NM_001135057.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr4:71698925 C>T maps to NM_002092.3 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr4:71698925 C>T maps to NM_002092.3 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr4:77662553 C>T maps to NM_020859.3 P1076P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr4:77662553 C>T maps to NM_020859.3 P1076P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr5:23522936 T>C maps to NM_020227.2 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr5:23522936 T>C maps to NM_020227.2 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr5:33576944 C>T maps to NM_030955.2 L1062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr5:33576944 C>T maps to NM_030955.2 L1062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr5:128983576 C>T maps to NM_133638.3 R658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr5:128983576 C>T maps to NM_133638.3 R658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr5:140564245 G>A maps to NM_020957.1 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr5:140564245 G>A maps to NM_020957.1 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr6:35088706 C>A maps to NM_001093728.1 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr6:35088706 C>A maps to NM_001093728.1 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr6:41899232 C>T maps to NM_004053.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr6:41899232 C>T maps to NM_004053.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr6:96053863 T>C maps to NM_024641.2 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr6:96053863 T>C maps to NM_024641.2 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr6:99883591 T>C maps to NM_001080481.1 *815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr6:99883591 T>C maps to NM_001080481.1 *815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr7:64438978 T>A maps to NM_015852.3 K324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr7:64438978 T>A maps to NM_015852.3 K324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr7:101845471 C>A maps to ENST00000360264 I976I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr7:101845471 C>A maps to ENST00000360264 I976I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr8:3059179 G>A maps to NM_033225.5 T1684T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr8:3059179 G>A maps to NM_033225.5 T1684T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr9:111617532 C>T maps to NM_006686.3 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr9:111617532 C>T maps to NM_006686.3 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chrX:44942703 G>A did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chrX:44942703 G>A did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chrX:70674607 T>C maps to ENST00000449580 T1612T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chrX:70674607 T>C maps to ENST00000449580 T1612T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:1120450 C>A maps to NM_001130045.1 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:1120450 C>A maps to NM_001130045.1 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:78390877 G>A maps to NM_144573.3 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:78390877 G>A maps to NM_144573.3 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:152595357 C>T maps to NM_178431.1 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:152595357 C>T maps to NM_178431.1 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:169390780 G>C maps to ENST00000367806 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:169390780 G>C maps to ENST00000367806 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:190423906 C>T maps to NM_199051.1 Q38Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:190423906 C>T maps to NM_199051.1 Q38Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:200522869 G>A maps to NM_014875.2 L1531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:200522869 G>A maps to NM_014875.2 L1531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:223116609 C>T maps to NM_032890.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:223116609 C>T maps to NM_032890.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:245848772 C>T maps to NM_018012.3 L830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr1:245848772 C>T maps to NM_018012.3 L830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr10:24896426 C>T did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr10:24896426 C>T did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr10:70847957 T>C maps to NM_002727.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr10:70847957 T>C maps to NM_002727.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr10:97916166 A>C maps to NM_014803.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr10:97916166 A>C maps to NM_014803.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr10:102267288 T>A maps to NM_015490.3 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr10:102267288 T>A maps to NM_015490.3 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr10:105349975 C>T maps to NM_004210.4 C524C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr10:105349975 C>T maps to NM_004210.4 C524C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr10:118896128 G>A maps to NM_001112704.1 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr10:118896128 G>A maps to NM_001112704.1 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr10:123730453 T>A maps to NM_017615.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr10:123730453 T>A maps to NM_017615.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr11:6662064 G>A maps to NM_003737.2 Y260Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr11:6662064 G>A maps to NM_003737.2 Y260Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr11:6662628 C>G maps to NM_003737.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr11:6662628 C>G maps to NM_003737.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr11:57155326 T>C maps to NM_002728.4 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr11:57155326 T>C maps to NM_002728.4 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr11:59245072 G>T maps to NM_001004705.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr11:59245072 G>T maps to NM_001004705.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr11:111593424 C>T maps to NM_015191.1 Q698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr11:111593424 C>T maps to NM_015191.1 Q698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr11:124180026 T>C maps to NM_001002917.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr11:124180026 T>C maps to NM_001002917.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr12:14018731 C>T maps to NM_000834.3 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr12:14018731 C>T maps to NM_000834.3 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr12:81719650 T>A did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr12:81719650 T>A did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr13:33701604 C>G maps to NM_178007.2 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr13:33701604 C>G maps to NM_178007.2 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr13:39435694 A>T maps to NM_207361.4 I2549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr13:39435694 A>T maps to NM_207361.4 I2549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr14:20295660 C>A maps to NM_001004723.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr14:20295660 C>A maps to NM_001004723.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr14:23609699 C>T maps to NM_012244.2 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr14:23609699 C>T maps to NM_012244.2 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr14:36003679 G>T maps to NM_032594.3 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr14:36003679 G>T maps to NM_032594.3 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr14:96937851 A>G maps to NM_152327.2 K465K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr14:96937851 A>G maps to NM_152327.2 K465K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr15:54306701 C>T maps to ENST00000260323 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr15:54306701 C>T maps to ENST00000260323 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr15:65491006 G>C maps to NM_003613.3 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr15:65491006 G>C maps to NM_003613.3 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr15:79382663 G>A maps to NM_002891.4 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr15:79382663 G>A maps to NM_002891.4 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr16:67425060 C>A did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr16:67425060 C>A did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr16:72984463 G>C maps to NM_006885.3 L1040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr16:72984463 G>C maps to NM_006885.3 L1040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr16:81298333 C>T maps to NM_017429.2 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr16:81298333 C>T maps to NM_017429.2 S187S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CV-7254-01A-11D-2012-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CV-7254-01A-11D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr17:26822749 C>T maps to NM_001145975.1 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr17:26822749 C>T maps to NM_001145975.1 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr17:40825795 G>A maps to NM_024927.4 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr17:40825795 G>A maps to NM_024927.4 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr17:48941306 A>G maps to NM_005749.2 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr17:48941306 A>G maps to NM_005749.2 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr18:9256147 G>A maps to NM_015208.3 K961K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr18:9256147 G>A maps to NM_015208.3 K961K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr19:1881346 A>G maps to NM_031213.3 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr19:1881346 A>G maps to NM_031213.3 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr19:6854108 G>T maps to NM_005428.2 R828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr19:6854108 G>T maps to NM_005428.2 R828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr19:10385696 C>A maps to NM_000201.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr19:10385696 C>A maps to NM_000201.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr19:40197265 T>C maps to NM_203471.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr19:40197265 T>C maps to NM_203471.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr19:45406350 G>A maps to NM_006114.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr19:45406350 G>A maps to NM_006114.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr19:56114032 G>A maps to NM_153219.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr19:56114032 G>A maps to NM_153219.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr2:98916585 T>C maps to NM_144992.4 F1109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr2:98916585 T>C maps to NM_144992.4 F1109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr2:100210205 C>T maps to NM_001025108.1 K664K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr2:100210205 C>T maps to NM_001025108.1 K664K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr2:120844791 G>A maps to NM_020909.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr2:120844791 G>A maps to NM_020909.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr2:197866544 C>T maps to NM_001195144.1 E789E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr2:197866544 C>T maps to NM_001195144.1 E789E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr2:198570155 G>T maps to NM_138395.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr2:198570155 G>T maps to NM_138395.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr2:219543984 G>T did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr2:219543984 G>T did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr20:2413287 G>T maps to NM_198994.2 *707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr20:2413287 G>T maps to NM_198994.2 *707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr20:7875860 G>T maps to NM_017545.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr20:7875860 G>T maps to NM_017545.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr21:11098775 C>A did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr21:11098775 C>A did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr22:45571833 A>G maps to NM_007172.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr22:45571833 A>G maps to NM_007172.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr3:36898413 C>A maps to NM_014831.2 R889R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr3:36898413 C>A maps to NM_014831.2 R889R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr3:40231704 G>A maps to NM_015460.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr3:40231704 G>A maps to NM_015460.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr3:112999436 C>A maps to ENST00000273395 I746I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr3:112999436 C>A maps to ENST00000273395 I746I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr3:137843690 G>T maps to NM_016161.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr3:137843690 G>T maps to NM_016161.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr4:55970954 G>T maps to NM_002253.2 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr4:55970954 G>T maps to NM_002253.2 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr4:89407342 A>G maps to NM_016323.2 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr4:89407342 A>G maps to NM_016323.2 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr4:111539442 G>C maps to NM_153426.1 Y264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr4:111539442 G>C maps to NM_153426.1 Y264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr4:119148126 C>A maps to NM_004784.2 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr4:119148126 C>A maps to NM_004784.2 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr5:422968 G>A maps to NM_020731.3 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr5:422968 G>A maps to NM_020731.3 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr5:70952609 C>T maps to NM_022132.4 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr5:70952609 C>T maps to NM_022132.4 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr5:75989260 G>T maps to NM_006633.2 A1329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr5:75989260 G>T maps to NM_006633.2 A1329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr6:31864039 C>T maps to ENST00000395728 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr6:31864039 C>T maps to ENST00000395728 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr7:7622857 G>A maps to NM_019005.3 K501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr7:7622857 G>A maps to NM_019005.3 K501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr7:45141454 G>A maps to ENST00000404564 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr7:45141454 G>A maps to ENST00000404564 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr7:92762800 T>C maps to NM_152703.2 R828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr7:92762800 T>C maps to NM_152703.2 R828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr7:98449122 C>T maps to NM_001134450.1 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr7:98449122 C>T maps to NM_001134450.1 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr7:112555358 A>G did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr7:112555358 A>G did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr7:141794548 G>T maps to ENST00000475668 T2449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr7:141794548 G>T maps to ENST00000475668 T2449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr8:42563959 T>C maps to NM_000749.3 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr8:42563959 T>C maps to NM_000749.3 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr8:139728520 G>T maps to NM_152888.1 G804G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr8:139728520 G>T maps to NM_152888.1 G804G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr9:21971028 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr9:21971028 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr9:34490413 C>A maps to NM_012144.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr9:34490413 C>A maps to NM_012144.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr9:71845072 G>C maps to NM_004817.3 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr9:71845072 G>C maps to NM_004817.3 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr9:71866154 G>T maps to NM_004817.3 E1066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr9:71866154 G>T maps to NM_004817.3 E1066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr9:77436730 G>T maps to NM_017662.4 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr9:77436730 G>T maps to NM_017662.4 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr9:133738361 G>A maps to NM_007313.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr9:133738361 G>A maps to NM_007313.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chrX:37651298 T>C maps to NM_000397.3 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chrX:37651298 T>C maps to NM_000397.3 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chrX:83411199 C>A did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chrX:83411199 C>A did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chrX:106312632 C>G did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chrX:106312632 C>G did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chrX:110576306 A>T maps to ENST00000358070 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chrX:110576306 A>T maps to ENST00000358070 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chrX:130408087 C>A maps to NM_001170961.1 E1287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chrX:130408087 C>A maps to NM_001170961.1 E1287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chrX:139038573 T>C maps to NM_001013403.2 E189E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chrX:139038573 T>C maps to NM_001013403.2 E189E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr1:43636550 C>T did not map to a codon.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr1:43636550 C>T did not map to a codon.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr1:117663358 G>A maps to NM_025188.3 C155C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr1:117663358 G>A maps to NM_025188.3 C155C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr11:1264976 C>T maps to ENST00000447027 S2292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr11:1264976 C>T maps to ENST00000447027 S2292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr11:1268747 C>T maps to ENST00000447027 S3549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr11:1268747 C>T maps to ENST00000447027 S3549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr11:73962724 G>A maps to NM_016147.1 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr11:73962724 G>A maps to NM_016147.1 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr11:88911069 C>G did not map to a codon.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr11:88911069 C>G did not map to a codon.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr11:105758285 C>A maps to NM_000829.3 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr11:105758285 C>A maps to NM_000829.3 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr12:55945873 T>C maps to NM_001005494.1 Y288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr12:55945873 T>C maps to NM_001005494.1 Y288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr12:133331318 C>T maps to NM_015114.1 K194K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr12:133331318 C>T maps to NM_015114.1 K194K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr13:45149169 A>G maps to NM_183422.2 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr13:45149169 A>G maps to NM_183422.2 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr14:74426167 A>C maps to NM_182476.1 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr14:74426167 A>C maps to NM_182476.1 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr16:89702703 G>A maps to NM_004413.3 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr16:89702703 G>A maps to NM_004413.3 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr17:40914815 C>T maps to ENST00000456272 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr17:40914815 C>T maps to ENST00000456272 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr18:9886721 C>T maps to NM_001098529.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr18:9886721 C>T maps to NM_001098529.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr18:13885466 A>G maps to NM_000529.2 N17N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr18:13885466 A>G maps to NM_000529.2 N17N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr19:40392568 G>A maps to NM_003890.2 S2645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr19:40392568 G>A maps to NM_003890.2 S2645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr19:57967605 C>T maps to NM_020633.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr19:57967605 C>T maps to NM_020633.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr20:33033214 T>C maps to ENST00000262650 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr20:33033214 T>C maps to ENST00000262650 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr20:56098319 C>T maps to ENST00000423479 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr20:56098319 C>T maps to ENST00000423479 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr4:7735047 G>A did not map to a codon.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr4:7735047 G>A did not map to a codon.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr4:146824263 C>T maps to ENST00000508784 Q49Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr4:146824263 C>T maps to ENST00000508784 Q49Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr5:16701456 G>C maps to NM_012334.2 S1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr5:16701456 G>C maps to NM_012334.2 S1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr5:101834431 C>T maps to NM_173488.3 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr5:101834431 C>T maps to NM_173488.3 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr5:153026581 C>T maps to NM_001114183.1 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr5:153026581 C>T maps to NM_001114183.1 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr7:1132134 G>A maps to NM_001505.2 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr7:1132134 G>A maps to NM_001505.2 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr7:30058664 C>A maps to NM_017946.2 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr7:30058664 C>A maps to NM_017946.2 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr7:100238306 A>G did not map to a codon.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr7:100238306 A>G did not map to a codon.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr7:128640536 C>T maps to ENST00000471166 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr7:128640536 C>T maps to ENST00000471166 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr8:92352727 T>C maps to NM_134266.1 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr8:92352727 T>C maps to NM_134266.1 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr8:113347672 G>A maps to NM_198123.1 I2350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chr8:113347672 G>A maps to NM_198123.1 I2350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chrX:54955307 C>A maps to NM_001039705.1 A717A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chrX:54955307 C>A maps to NM_001039705.1 A717A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chrX:57619371 C>T maps to NM_007157.3 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chrX:57619371 C>T maps to NM_007157.3 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chrX:57936695 G>A maps to NM_007156.4 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chrX:57936695 G>A maps to NM_007156.4 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chrX:77112871 G>A maps to NM_032121.5 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7255-01A-11D-2012-08 chrX:77112871 G>A maps to NM_032121.5 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr1:22313088 C>G maps to NM_007352.2 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr1:22313088 C>G maps to NM_007352.2 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr1:147092753 T>A maps to NM_004326.2 P931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr1:147092753 T>A maps to NM_004326.2 P931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr1:156616599 C>T maps to NM_021948.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr1:156616599 C>T maps to NM_021948.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr1:157776892 G>A maps to NM_052938.4 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr1:157776892 G>A maps to NM_052938.4 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr1:159409808 C>T maps to NM_012351.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr1:159409808 C>T maps to NM_012351.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr1:197390385 C>T maps to NM_201253.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr1:197390385 C>T maps to NM_201253.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr11:7324588 G>A maps to NM_175733.3 Q155Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr11:7324588 G>A maps to NM_175733.3 Q155Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr11:26587443 C>T did not map to a codon.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr11:26587443 C>T did not map to a codon.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr11:58322349 A>G maps to NM_004811.2 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr11:58322349 A>G maps to NM_004811.2 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr12:100173679 C>T maps to NM_152788.3 Q272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr12:100173679 C>T maps to NM_152788.3 Q272Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr14:66136077 C>T maps to NM_178155.1 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr14:66136077 C>T maps to NM_178155.1 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr14:100793679 C>G maps to NM_207117.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr14:100793679 C>G maps to NM_207117.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr16:1561082 C>T maps to NM_014714.3 P1417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr16:1561082 C>T maps to NM_014714.3 P1417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr17:44110826 C>T did not map to a codon.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr17:44110826 C>T did not map to a codon.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr17:79804355 C>T maps to NM_000918.3 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr17:79804355 C>T maps to NM_000918.3 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr19:9045869 C>A maps to NM_024690.2 E11921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr19:9045869 C>A maps to NM_024690.2 E11921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr2:54133993 T>C maps to NM_014614.2 K932K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr2:54133993 T>C maps to NM_014614.2 K932K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr2:141093260 C>T maps to NM_018557.2 L4013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr2:141093260 C>T maps to NM_018557.2 L4013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr2:168102824 A>G maps to NM_152381.5 L1641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr2:168102824 A>G maps to NM_152381.5 L1641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr20:9546782 C>T maps to NM_177990.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr20:9546782 C>T maps to NM_177990.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr20:62657404 C>T maps to NM_012469.3 T674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr20:62657404 C>T maps to NM_012469.3 T674T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr22:22127163 C>A maps to NM_138957.2 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr22:22127163 C>A maps to NM_138957.2 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr3:126747876 G>T maps to NM_032242.3 E1571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr3:126747876 G>T maps to NM_032242.3 E1571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr3:129182444 C>G maps to NM_052985.2 S182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr3:129182444 C>G maps to NM_052985.2 S182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr3:164727147 G>A maps to NM_001041.3 F1366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr3:164727147 G>A maps to NM_001041.3 F1366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr6:126080845 C>T maps to NM_012259.2 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr6:126080845 C>T maps to NM_012259.2 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr6:126080848 G>T maps to NM_012259.2 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr6:126080848 G>T maps to NM_012259.2 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr6:133783511 A>G maps to ENST00000452339 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr6:133783511 A>G maps to ENST00000452339 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr7:86394697 C>T maps to NM_000840.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr7:86394697 C>T maps to NM_000840.2 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr7:87037430 C>A maps to NM_018849.2 L1067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr7:87037430 C>A maps to NM_018849.2 L1067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr7:142724093 C>T maps to NM_001001658.1 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr7:142724093 C>T maps to NM_001001658.1 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr8:39624379 G>A maps to NM_001464.3 D498D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr8:39624379 G>A maps to NM_001464.3 D498D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr8:55534742 A>T maps to NM_006269.1 K228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr8:55534742 A>T maps to NM_006269.1 K228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr8:139190885 C>A maps to NM_015912.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr8:139190885 C>A maps to NM_015912.3 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr9:125585306 C>T maps to NM_005388.4 K114K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr9:125585306 C>T maps to NM_005388.4 K114K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr9:131022970 G>A maps to NM_004486.4 Q484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr9:131022970 G>A maps to NM_004486.4 Q484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr9:136573441 G>A maps to NM_007101.3 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr9:136573441 G>A maps to NM_007101.3 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chrX:69673591 A>G maps to ENST00000194900 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chrX:69673591 A>G maps to ENST00000194900 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chrX:100617675 T>A maps to NM_000061.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chrX:100617675 T>A maps to NM_000061.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chrX:100617677 C>A did not map to a codon.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chrX:100617677 C>A did not map to a codon.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr1:11854026 G>A maps to ENST00000376585 N530N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr1:11854026 G>A maps to ENST00000376585 N530N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr1:36785373 C>T maps to NM_001162530.1 N370N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr1:36785373 C>T maps to NM_001162530.1 N370N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr1:46751226 T>C maps to ENST00000254454 E412E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr1:46751226 T>C maps to ENST00000254454 E412E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr1:119683179 G>A maps to NM_015836.3 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr1:119683179 G>A maps to NM_015836.3 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr1:158669806 C>T maps to NM_001005279.1 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr1:158669806 C>T maps to NM_001005279.1 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr1:198665839 G>A did not map to a codon.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr1:198665839 G>A did not map to a codon.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr10:98742211 C>T maps to NM_015652.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr10:98742211 C>T maps to NM_015652.2 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr10:121212265 C>T maps to NM_005308.2 D496D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr10:121212265 C>T maps to NM_005308.2 D496D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr11:67134939 A>T maps to NM_013246.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr11:67134939 A>T maps to NM_013246.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr11:102480738 G>A maps to NM_004771.3 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr11:102480738 G>A maps to NM_004771.3 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr11:117303095 G>A maps to NM_020693.2 I1777I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr11:117303095 G>A maps to NM_020693.2 I1777I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr12:69083343 T>C maps to NM_020401.2 N44N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr12:69083343 T>C maps to NM_020401.2 N44N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr12:112940024 T>C maps to ENST00000392596 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr12:112940024 T>C maps to ENST00000392596 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr14:64522879 C>T maps to NM_182914.2 S3321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr14:64522879 C>T maps to NM_182914.2 S3321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr17:3819556 C>T did not map to a codon.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr17:3819556 C>T did not map to a codon.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr17:7579377 G>C maps to NM_001126112.1 Y103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr17:7579377 G>C maps to NM_001126112.1 Y103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr17:7802767 G>A maps to NM_001005271.2 T876T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr17:7802767 G>A maps to NM_001005271.2 T876T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr18:61074673 G>A maps to NM_004869.3 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr18:61074673 G>A maps to NM_004869.3 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr19:54080197 G>A maps to NM_001079907.1 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr19:54080197 G>A maps to NM_001079907.1 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr2:50149200 G>A maps to ENST00000404971 R1509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr2:50149200 G>A maps to ENST00000404971 R1509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr2:172942596 T>C maps to NM_199227.1 H259H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr2:172942596 T>C maps to NM_199227.1 H259H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr2:220098106 C>T maps to NM_001042410.1 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr2:220098106 C>T maps to NM_001042410.1 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr3:49933238 C>T maps to NM_002447.2 T957T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr3:49933238 C>T maps to NM_002447.2 T957T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CV-7263-01A-11D-2012-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-CV-7263-01A-11D-2012-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr4:187540844 C>A maps to ENST00000260147 G2302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr4:187540844 C>A maps to ENST00000260147 G2302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr7:88964788 C>T maps to NM_181646.2 N831N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr7:88964788 C>T maps to NM_181646.2 N831N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr7:100678302 A>C maps to NM_001040105.1 P1202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr7:100678302 A>C maps to NM_001040105.1 P1202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr7:150556007 C>T maps to ENST00000416793 Y576Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr7:150556007 C>T maps to ENST00000416793 Y576Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr8:70674021 A>G maps to NM_030958.2 N332N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr8:70674021 A>G maps to NM_030958.2 N332N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr8:133596001 G>A maps to ENST00000250173 Q389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr8:133596001 G>A maps to ENST00000250173 Q389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr9:125330735 G>T maps to NM_001004454.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr9:125330735 G>T maps to NM_001004454.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr2:27688749 C>A did not map to a codon.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr2:27688749 C>A did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr1:54423864 C>A maps to NM_052940.3 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr1:54423864 C>A maps to NM_052940.3 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr1:86919184 G>T maps to NM_006536.5 V763V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr1:86919184 G>T maps to NM_006536.5 V763V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr1:160303418 C>T maps to NM_001098398.1 W120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr1:160303418 C>T maps to NM_001098398.1 W120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr1:169525914 G>A maps to ENST00000367796 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr1:169525914 G>A maps to ENST00000367796 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr1:179063233 C>T maps to NM_022371.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr1:179063233 C>T maps to NM_022371.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr10:35929478 G>A maps to NM_031866.2 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr10:35929478 G>A maps to NM_031866.2 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr10:102510538 G>T maps to NM_003987.3 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr10:102510538 G>T maps to NM_003987.3 E101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr11:55606667 G>A maps to NM_001005496.1 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr11:55606667 G>A maps to NM_001005496.1 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr11:94861542 C>T maps to NM_015036.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr11:94861542 C>T maps to NM_015036.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr11:102593221 G>A maps to NM_002424.2 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr11:102593221 G>A maps to NM_002424.2 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr12:8212580 C>T maps to NM_004054.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr12:8212580 C>T maps to NM_004054.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr12:15742397 G>A maps to NM_030667.1 V1140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr12:15742397 G>A maps to NM_030667.1 V1140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr12:106708239 C>T maps to NM_152772.1 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr12:106708239 C>T maps to NM_152772.1 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr13:67801806 G>A maps to NM_203487.2 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr13:67801806 G>A maps to NM_203487.2 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr14:80669403 G>A maps to NM_001007023.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr14:80669403 G>A maps to NM_001007023.2 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr14:88477469 C>T maps to NM_003608.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr14:88477469 C>T maps to NM_003608.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr14:93709137 G>A maps to NM_001002860.2 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr14:93709137 G>A maps to NM_001002860.2 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr15:42019555 C>T maps to ENST00000219905 L1203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr15:42019555 C>T maps to ENST00000219905 L1203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr15:72502753 G>A maps to ENST00000419739 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr15:72502753 G>A maps to ENST00000419739 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr15:99758830 C>T maps to NM_022905.4 W181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr15:99758830 C>T maps to NM_022905.4 W181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr16:2376269 C>T maps to NM_001089.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr16:2376269 C>T maps to NM_001089.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr16:3614472 C>T maps to ENST00000448023 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr16:3614472 C>T maps to ENST00000448023 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr16:66945109 C>G maps to NM_004062.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr16:66945109 C>G maps to NM_004062.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr17:10301954 G>A maps to NM_002472.2 A1328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr17:10301954 G>A maps to NM_002472.2 A1328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr17:17891327 G>A maps to NM_031294.3 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr17:17891327 G>A maps to NM_031294.3 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr17:40574758 G>A maps to NM_012232.5 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr17:40574758 G>A maps to NM_012232.5 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr17:42786684 C>T maps to NM_145663.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr17:42786684 C>T maps to NM_145663.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr17:76134711 G>A maps to NM_152468.4 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr17:76134711 G>A maps to NM_152468.4 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr17:78882728 G>A maps to NM_020761.2 K840K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr17:78882728 G>A maps to NM_020761.2 K840K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr17:80863818 G>A maps to NM_005993.4 P604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr17:80863818 G>A maps to NM_005993.4 P604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr18:202938 C>T maps to NM_005151.3 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr18:202938 C>T maps to NM_005151.3 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:20728761 G>A maps to NM_001159293.1 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:20728761 G>A maps to NM_001159293.1 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:40354268 G>A maps to NM_003890.2 F5400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:40354268 G>A maps to NM_003890.2 F5400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:42221506 G>A maps to NM_004363.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:42221506 G>A maps to NM_004363.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:42510940 G>A maps to NM_002088.3 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:42510940 G>A maps to NM_002088.3 I631I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:44222838 C>A maps to NM_019612.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:44222838 C>A maps to NM_019612.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:45769535 G>A maps to NM_031417.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:45769535 G>A maps to NM_031417.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:54819016 G>C maps to NM_021250.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:54819016 G>C maps to NM_021250.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:57133428 C>T maps to NM_021216.4 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr19:57133428 C>T maps to NM_021216.4 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr2:71046979 C>T maps to NM_173535.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr2:71046979 C>T maps to NM_173535.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr2:74734012 T>C did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr2:74734012 T>C did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr2:80530935 G>A maps to NM_178839.4 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr2:80530935 G>A maps to NM_178839.4 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr2:158115562 G>C maps to NM_014568.1 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr2:158115562 G>C maps to NM_014568.1 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr2:191874722 G>A maps to NM_007315.3 Q3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr2:191874722 G>A maps to NM_007315.3 Q3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr20:372178 G>A maps to ENST00000422053 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr20:372178 G>A maps to ENST00000422053 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr20:35668561 G>A maps to NM_002895.2 R633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr20:35668561 G>A maps to NM_002895.2 R633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr21:43547844 C>T maps to NM_173568.3 F1326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr21:43547844 C>T maps to NM_173568.3 F1326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr22:30722747 G>A maps to ENST00000403477 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr22:30722747 G>A maps to ENST00000403477 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:11059595 C>T maps to NM_003042.3 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:11059595 C>T maps to NM_003042.3 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:119528934 G>A maps to NM_022002.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:119528934 G>A maps to NM_022002.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:127642956 G>A maps to NM_207335.2 K351K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:127642956 G>A maps to NM_207335.2 K351K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:183756392 C>T maps to NM_001145143.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:183756392 C>T maps to NM_001145143.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:184005698 C>T maps to NM_014693.3 F564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:184005698 C>T maps to NM_014693.3 F564F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:194362967 C>G maps to NM_018385.2 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:194362967 C>G maps to NM_018385.2 V602V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:194991444 G>A maps to NM_152531.4 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr3:194991444 G>A maps to NM_152531.4 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr4:72397810 C>T maps to NM_001098484.2 I733I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr4:72397810 C>T maps to NM_001098484.2 I733I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr4:155530880 C>T maps to ENST00000407946 Q197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr4:155530880 C>T maps to ENST00000407946 Q197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:14368962 C>G maps to NM_007118.2 L1007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:14368962 C>G maps to NM_007118.2 L1007L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:45353207 C>T maps to NM_021072.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:45353207 C>T maps to NM_021072.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:89943366 C>T maps to NM_032119.3 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:89943366 C>T maps to NM_032119.3 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:94876456 C>T maps to NM_014639.3 W160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:94876456 C>T maps to NM_014639.3 W160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:139192995 C>T maps to NM_032289.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:139192995 C>T maps to NM_032289.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:140735360 C>T maps to NM_018917.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:140735360 C>T maps to NM_018917.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:141694649 G>A maps to NM_030964.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:141694649 G>A maps to NM_030964.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:158140038 C>T maps to NM_024007.3 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:158140038 C>T maps to NM_024007.3 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:167645221 G>A maps to NM_001122679.1 E1433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr5:167645221 G>A maps to NM_001122679.1 E1433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr6:105224985 C>G did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr6:105224985 C>G did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr7:99704399 C>G maps to ENST00000429084 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr7:99704399 C>G maps to ENST00000429084 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr8:67066570 T>G did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr8:67066570 T>G did not map to a codon.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr8:145154327 G>A maps to NM_030974.3 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr8:145154327 G>A maps to NM_030974.3 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr9:36169708 C>T maps to NM_005893.2 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr9:36169708 C>T maps to NM_005893.2 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chrX:48650431 G>A maps to NM_002049.3 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chrX:48650431 G>A maps to NM_002049.3 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chrX:78616832 G>A maps to NM_004867.4 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chrX:78616832 G>A maps to NM_004867.4 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chrX:132795856 C>T maps to NM_001164617.1 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chrX:132795856 C>T maps to NM_001164617.1 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr8:132052291 C>T maps to NM_001115.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7406-01A-11D-2078-08 chr8:132052291 C>T maps to NM_001115.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:16059014 C>G maps to ENST00000420314 Y1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:16059014 C>G maps to ENST00000420314 Y1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:86361733 A>G maps to NM_152890.5 D949D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:86361733 A>G maps to NM_152890.5 D949D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:151373788 C>A maps to NM_002796.2 C217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:151373788 C>A maps to NM_002796.2 C217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:152856942 C>T maps to NM_030663.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:152856942 C>T maps to NM_030663.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:166818316 G>A maps to NM_017542.3 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:166818316 G>A maps to NM_017542.3 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:171249963 C>T maps to NM_002021.1 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:171249963 C>T maps to NM_002021.1 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:205888027 G>A maps to NM_134325.2 D732D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:205888027 G>A maps to NM_134325.2 D732D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:232600687 T>C maps to NM_020808.3 G906G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr1:232600687 T>C maps to NM_020808.3 G906G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr10:47087865 C>A maps to NM_005972.4 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr10:47087865 C>A maps to NM_005972.4 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr10:48428781 C>T maps to NM_004962.2 K368K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr10:48428781 C>T maps to NM_004962.2 K368K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr11:18158850 G>A maps to NM_054031.3 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr11:18158850 G>A maps to NM_054031.3 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr11:22696394 G>A did not map to a codon.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr11:22696394 G>A did not map to a codon.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr11:62298957 G>A maps to NM_001620.1 G977G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr11:62298957 G>A maps to NM_001620.1 G977G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr11:64361158 T>C maps to NM_144585.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr11:64361158 T>C maps to NM_144585.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr11:107427561 G>A maps to ENST00000417449 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr11:107427561 G>A maps to ENST00000417449 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr12:653524 G>A maps to NM_173593.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr12:653524 G>A maps to NM_173593.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr12:129569217 G>T maps to NM_133448.2 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr12:129569217 G>T maps to NM_133448.2 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr14:93412778 G>A maps to NM_014216.4 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr14:93412778 G>A maps to NM_014216.4 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr16:830538 C>T maps to NM_001025190.1 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr16:830538 C>T maps to NM_001025190.1 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr17:8197903 G>A maps to NM_201520.1 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr17:8197903 G>A maps to NM_201520.1 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr17:32483503 G>A maps to NM_001094.4 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr17:32483503 G>A maps to NM_001094.4 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr19:8618064 G>A maps to NM_012335.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr19:8618064 G>A maps to NM_012335.3 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr19:49933916 G>A maps to NM_020309.3 D514D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr19:49933916 G>A maps to NM_020309.3 D514D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr2:1653340 G>A maps to NM_012293.1 F737F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr2:1653340 G>A maps to NM_012293.1 F737F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr2:1664728 T>C maps to NM_012293.1 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr2:1664728 T>C maps to NM_012293.1 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr2:21231327 G>A maps to NM_000384.2 L2804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr2:21231327 G>A maps to NM_000384.2 L2804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr2:70408541 T>C maps to NM_017880.1 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr2:70408541 T>C maps to NM_017880.1 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr2:153471450 A>G maps to NM_052905.3 E383E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr2:153471450 A>G maps to NM_052905.3 E383E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr2:242401975 G>A maps to NM_014808.2 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr2:242401975 G>A maps to NM_014808.2 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr21:45730966 G>T did not map to a codon.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr21:45730966 G>T did not map to a codon.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr22:22988943 C>G maps to ENST00000215938 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr22:22988943 C>G maps to ENST00000215938 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr22:32011158 C>G maps to NM_001007467.1 S1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr22:32011158 C>G maps to NM_001007467.1 S1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr22:32650128 C>T maps to NM_014227.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr22:32650128 C>T maps to NM_014227.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr3:147128516 G>A maps to NM_003412.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr3:147128516 G>A maps to NM_003412.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr3:164741543 T>A maps to NM_001041.3 A971A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr3:164741543 T>A maps to NM_001041.3 A971A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr4:185340659 T>C maps to NM_002199.3 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr4:185340659 T>C maps to NM_002199.3 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr5:170668103 T>G maps to NM_022897.3 A865A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr5:170668103 T>G maps to NM_022897.3 A865A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr6:27833179 G>A maps to NM_003511.2 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr6:27833179 G>A maps to NM_003511.2 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr6:28268548 G>A maps to NM_032507.3 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr6:28268548 G>A maps to NM_032507.3 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr6:90482424 G>A maps to NM_014611.1 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr6:90482424 G>A maps to NM_014611.1 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr6:152651116 C>T maps to NM_182961.2 R4901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr6:152651116 C>T maps to NM_182961.2 R4901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr7:101559502 G>T maps to ENST00000360264 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr7:101559502 G>T maps to ENST00000360264 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr7:121943894 G>A maps to NM_001024613.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr7:121943894 G>A maps to NM_001024613.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr7:126883114 C>T maps to NM_001127323.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr7:126883114 C>T maps to NM_001127323.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr8:77764067 C>T maps to NM_024721.4 S1637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr8:77764067 C>T maps to NM_024721.4 S1637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr9:14842545 G>A maps to ENST00000380880 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr9:14842545 G>A maps to ENST00000380880 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr9:86495229 C>T maps to NM_017576.1 R875R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr9:86495229 C>T maps to NM_017576.1 R875R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr9:97897695 C>A maps to NM_000136.2 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chr9:97897695 C>A maps to NM_000136.2 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chrX:18660204 G>A maps to NM_000330.3 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chrX:18660204 G>A maps to NM_000330.3 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chrX:50134544 G>A maps to NM_001013742.1 T578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chrX:50134544 G>A maps to NM_001013742.1 T578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chrX:138680606 G>C maps to ENST00000370578 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7407-01A-11D-2078-08 chrX:138680606 G>C maps to ENST00000370578 L774L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr1:1961582 C>A maps to NM_000815.4 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr1:1961582 C>A maps to NM_000815.4 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr1:74507573 G>T maps to NM_001105659.1 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr1:74507573 G>T maps to NM_001105659.1 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr1:89418757 T>A maps to NM_001008661.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr1:89418757 T>A maps to NM_001008661.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr1:151210742 T>C did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr1:151210742 T>C did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr10:99213335 T>C maps to NM_198046.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr10:99213335 T>C maps to NM_198046.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr11:55606283 C>T maps to NM_001005496.1 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr11:55606283 C>T maps to NM_001005496.1 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr11:55798049 T>C maps to NM_001001921.1 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr11:55798049 T>C maps to NM_001001921.1 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr11:121008260 C>T maps to NM_005422.2 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr11:121008260 C>T maps to NM_005422.2 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr11:124412749 G>C maps to NM_001005195.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr11:124412749 G>C maps to NM_001005195.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr11:134217281 G>T maps to NM_138342.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr11:134217281 G>T maps to NM_138342.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr13:109793137 C>T maps to NM_015011.1 P1504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr13:109793137 C>T maps to NM_015011.1 P1504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr15:28235775 C>A maps to NM_000275.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr15:28235775 C>A maps to NM_000275.2 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr15:40584264 C>T maps to NM_004573.2 E842E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr15:40584264 C>T maps to NM_004573.2 E842E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr15:63014679 G>A maps to NM_015059.2 S1040S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr15:63014679 G>A maps to NM_015059.2 S1040S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr15:65447146 C>T maps to NM_006660.3 Q528Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr15:65447146 C>T maps to NM_006660.3 Q528Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr16:31051060 C>T maps to NM_004604.3 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr16:31051060 C>T maps to NM_004604.3 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr16:54319492 C>T maps to NM_024336.2 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr16:54319492 C>T maps to NM_024336.2 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr16:75033820 G>A maps to ENST00000320619 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr16:75033820 G>A maps to ENST00000320619 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr17:1650636 C>A maps to NM_000934.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr17:1650636 C>A maps to NM_000934.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr17:40967927 G>A maps to NM_003766.3 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr17:40967927 G>A maps to NM_003766.3 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr17:56787302 T>C maps to NM_058216.1 N263N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr17:56787302 T>C maps to NM_058216.1 N263N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr18:44559811 G>T maps to NM_016427.2 Y608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr18:44559811 G>T maps to NM_016427.2 Y608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr18:50432615 G>T maps to NM_005215.3 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr18:50432615 G>T maps to NM_005215.3 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr19:1005350 C>A maps to NM_138690.1 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr19:1005350 C>A maps to NM_138690.1 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr19:4792849 G>A maps to NM_018708.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr19:4792849 G>A maps to NM_018708.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr19:9580304 C>T did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr19:9580304 C>T did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr19:17768872 G>T maps to ENST00000428389 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr19:17768872 G>T maps to ENST00000428389 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr19:21477071 A>G maps to NM_021269.2 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr19:21477071 A>G maps to NM_021269.2 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr19:44635981 T>A maps to NM_013362.2 C405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr19:44635981 T>A maps to NM_013362.2 C405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr2:179463658 G>C maps to NM_133378.4 T16358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr2:179463658 G>C maps to NM_133378.4 T16358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr2:196750876 G>A maps to NM_018897.2 Y1842Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr2:196750876 G>A maps to NM_018897.2 Y1842Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr2:200193506 G>A maps to NM_001172509.1 Q434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr2:200193506 G>A maps to NM_001172509.1 Q434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr2:219602783 C>T maps to NM_014640.4 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr2:219602783 C>T maps to NM_014640.4 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr2:238275605 G>T maps to NM_004369.3 R1742R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr2:238275605 G>T maps to NM_004369.3 R1742R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr20:44686241 T>A maps to NM_001134771.1 *1140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr20:44686241 T>A maps to NM_001134771.1 *1140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr22:50987548 A>G maps to NM_138433.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr22:50987548 A>G maps to NM_138433.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr3:9512327 G>A maps to ENST00000407969 V989V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr3:9512327 G>A maps to ENST00000407969 V989V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr3:33099620 C>A maps to NM_000404.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr3:33099620 C>A maps to NM_000404.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr3:67058733 G>T maps to NM_032505.2 R577R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr3:67058733 G>T maps to NM_032505.2 R577R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr3:107097153 C>T maps to NM_032600.2 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr3:107097153 C>T maps to NM_032600.2 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr3:135721836 T>C maps to NM_002718.4 D499D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr3:135721836 T>C maps to NM_002718.4 D499D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:74274381 C>A maps to NM_000477.5 C114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:74274381 C>A maps to NM_000477.5 C114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:90874517 C>A maps to NM_007351.2 A1212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:90874517 C>A maps to NM_007351.2 A1212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:104512795 G>T maps to NM_001059.2 C311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:104512795 G>T maps to NM_001059.2 C311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:141888962 C>A maps to NM_020724.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:141888962 C>A maps to NM_020724.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:145580833 G>C maps to NM_022475.1 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:145580833 G>C maps to NM_022475.1 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:155176798 A>G maps to NM_017639.3 S1816S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:155176798 A>G maps to NM_017639.3 S1816S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:156858587 T>C maps to NM_001334.2 Q200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:156858587 T>C maps to NM_001334.2 Q200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:175896993 G>T maps to NM_014269.4 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr4:175896993 G>T maps to NM_014269.4 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr5:33937333 C>A maps to NM_016568.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr5:33937333 C>A maps to NM_016568.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr5:126732332 G>T maps to NM_032446.2 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr5:126732332 G>T maps to NM_032446.2 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr5:176638856 C>T maps to NM_022455.4 Q1153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr5:176638856 C>T maps to NM_022455.4 Q1153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr6:72970464 T>C maps to NM_014989.4 T1037T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr6:72970464 T>C maps to NM_014989.4 T1037T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr6:127471622 T>A maps to ENST00000368317 C114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr6:127471622 T>A maps to ENST00000368317 C114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr6:152539538 C>A did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr6:152539538 C>A did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:28547349 A>T maps to NM_182898.2 K96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:28547349 A>T maps to NM_182898.2 K96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:31682744 C>A maps to NM_194300.2 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:31682744 C>A maps to NM_194300.2 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:84649547 C>A did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:84649547 C>A did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:91630491 C>A maps to NM_005751.4 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:91630491 C>A maps to NM_005751.4 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:97874005 C>G did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:97874005 C>G did not map to a codon.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:131848900 C>A maps to NM_020911.1 L1500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr7:131848900 C>A maps to NM_020911.1 L1500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr8:24167433 A>T maps to NM_014265.4 K60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr8:24167433 A>T maps to NM_014265.4 K60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr8:101300160 G>C maps to NM_183419.1 S81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr8:101300160 G>C maps to NM_183419.1 S81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr8:108334193 G>T maps to NM_001146.3 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr8:108334193 G>T maps to NM_001146.3 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr9:21970999 C>A maps to NM_001195132.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr9:21970999 C>A maps to NM_001195132.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr9:78710972 G>T maps to NM_001190482.1 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr9:78710972 G>T maps to NM_001190482.1 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr9:113228229 T>A maps to ENST00000374463 P1079P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chr9:113228229 T>A maps to ENST00000374463 P1079P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chrX:47775779 G>T maps to NM_007137.3 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chrX:47775779 G>T maps to NM_007137.3 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chrX:100087824 C>T maps to ENST00000415585 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chrX:100087824 C>T maps to ENST00000415585 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chrX:154490408 G>T maps to NM_171998.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7409-01A-31D-2229-08 chrX:154490408 G>T maps to NM_171998.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr10:13481366 G>C maps to ENST00000396900 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr10:13481366 G>C maps to ENST00000396900 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr12:66641853 C>G maps to NM_007199.2 S565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr12:66641853 C>G maps to NM_007199.2 S565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr15:81295190 C>T maps to NM_022566.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr15:81295190 C>T maps to NM_022566.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr15:83447593 T>C maps to NM_001007122.2 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr15:83447593 T>C maps to NM_001007122.2 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr16:17211719 C>T maps to NM_022166.3 V780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr16:17211719 C>T maps to NM_022166.3 V780V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr16:84488580 C>G maps to ENST00000416219 S713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr16:84488580 C>G maps to ENST00000416219 S713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr2:55894994 A>G did not map to a codon.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr2:55894994 A>G did not map to a codon.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr2:179635015 C>G maps to NM_133378.4 V2804V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr2:179635015 C>G maps to NM_133378.4 V2804V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr2:234975871 C>T maps to NM_006944.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr2:234975871 C>T maps to NM_006944.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr6:159457884 G>A maps to NM_054114.3 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr6:159457884 G>A maps to NM_054114.3 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr7:143140946 G>A maps to NM_177437.1 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr7:143140946 G>A maps to NM_177437.1 K134K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr9:129642754 T>C maps to ENST00000319119 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7410-01A-21D-2078-08 chr9:129642754 T>C maps to ENST00000319119 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr1:16385162 C>T maps to NM_182623.2 Q204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr1:16385162 C>T maps to NM_182623.2 Q204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr1:36929440 G>C maps to NM_031280.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr1:36929440 G>C maps to NM_031280.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr1:151377601 G>C maps to NM_015100.3 V1303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr1:151377601 G>C maps to NM_015100.3 V1303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr1:157665836 G>T maps to NM_052939.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr1:157665836 G>T maps to NM_052939.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr1:208202359 C>A maps to NM_025179.3 V1751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr1:208202359 C>A maps to NM_025179.3 V1751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr1:248112338 C>T maps to NM_001001963.1 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr1:248112338 C>T maps to NM_001001963.1 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr10:30316131 G>C maps to NM_020848.2 S982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr10:30316131 G>C maps to NM_020848.2 S982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr10:61834986 G>T maps to NM_020987.2 P1884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr10:61834986 G>T maps to NM_020987.2 P1884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr10:104164417 G>A maps to NM_002779.3 P874P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr10:104164417 G>A maps to NM_002779.3 P874P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr11:73689423 G>C did not map to a codon.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr11:73689423 G>C did not map to a codon.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr11:117152362 G>A maps to NM_207343.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr11:117152362 G>A maps to NM_207343.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr12:31242844 G>A maps to NM_030653.3 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr12:31242844 G>A maps to NM_030653.3 E302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr12:120588997 C>A maps to NM_006836.1 A1420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr12:120588997 C>A maps to NM_006836.1 A1420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr13:24465688 C>A maps to NM_001007537.1 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr13:24465688 C>A maps to NM_001007537.1 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr13:99376167 G>A maps to NM_005073.3 H121H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr13:99376167 G>A maps to NM_005073.3 H121H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr15:34115204 A>G maps to NM_001036.3 L3668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr15:34115204 A>G maps to NM_001036.3 L3668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr15:59350643 C>T maps to ENST00000434298 Q421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr15:59350643 C>T maps to ENST00000434298 Q421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr17:7907215 G>A maps to NM_000180.3 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr17:7907215 G>A maps to NM_000180.3 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr17:40997731 A>T maps to NM_009590.2 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr17:40997731 A>T maps to NM_009590.2 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr18:29104785 G>T maps to NM_001943.3 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr18:29104785 G>T maps to NM_001943.3 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr19:6416662 T>A did not map to a codon.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr19:6416662 T>A did not map to a codon.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr19:56244752 C>T maps to NM_176820.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr19:56244752 C>T maps to NM_176820.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr2:99013276 G>A maps to NM_001298.2 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr2:99013276 G>A maps to NM_001298.2 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr2:233243765 C>T maps to NM_001632.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr2:233243765 C>T maps to NM_001632.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr2:240984615 G>A maps to NM_173351.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr2:240984615 G>A maps to NM_173351.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr20:402810 G>T maps to NM_031229.2 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr20:402810 G>T maps to NM_031229.2 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr20:61978194 G>A maps to NM_000744.5 Y593Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr20:61978194 G>A maps to NM_000744.5 Y593Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr22:30887572 G>A maps to NM_174977.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr22:30887572 G>A maps to NM_174977.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr22:42322237 G>C maps to NM_052945.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr22:42322237 G>C maps to NM_052945.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr3:52552019 G>C did not map to a codon.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr3:52552019 G>C did not map to a codon.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr4:48523207 C>A maps to NM_015030.1 E2516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr4:48523207 C>A maps to NM_015030.1 E2516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr4:56823518 G>A maps to NM_025009.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr4:56823518 G>A maps to NM_025009.3 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr5:70948525 G>T maps to NM_022132.4 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr5:70948525 G>T maps to NM_022132.4 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr5:140476701 C>T maps to NM_018936.2 F776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr5:140476701 C>T maps to NM_018936.2 F776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr5:150027824 C>T maps to NM_001166209.1 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr5:150027824 C>T maps to NM_001166209.1 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr6:132195425 A>G maps to NM_006208.2 K528K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr6:132195425 A>G maps to NM_006208.2 K528K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr7:18788640 C>T maps to NM_178425.2 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr7:18788640 C>T maps to NM_178425.2 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr8:36673193 C>G maps to NM_001031836.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr8:36673193 C>G maps to NM_001031836.2 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr9:100137789 C>A maps to ENST00000375206 L1576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr9:100137789 C>A maps to ENST00000375206 L1576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr9:121971049 G>A maps to NM_014618.2 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr9:121971049 G>A maps to NM_014618.2 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr9:139401393 G>T maps to NM_017617.3 C1225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chr9:139401393 G>T maps to NM_017617.3 C1225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chrX:118222747 G>A maps to NM_020721.1 F815F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chrX:118222747 G>A maps to NM_020721.1 F815F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chrX:153135916 G>A maps to NM_000425.3 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7411-01A-11D-2078-08 chrX:153135916 G>A maps to NM_000425.3 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr1:10239992 G>A maps to NM_001105562.2 E1296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr1:10239992 G>A maps to NM_001105562.2 E1296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr1:167095879 G>A maps to NM_001080426.1 A504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr1:167095879 G>A maps to NM_001080426.1 A504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr10:11370982 G>A maps to NM_006561.3 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr10:11370982 G>A maps to NM_006561.3 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr12:7469846 C>T maps to NM_001080454.1 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr12:7469846 C>T maps to NM_001080454.1 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr12:55945681 G>T maps to NM_001005494.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr12:55945681 G>T maps to NM_001005494.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr12:113444281 A>G maps to NM_016817.2 K511K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr12:113444281 A>G maps to NM_016817.2 K511K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr16:15128327 G>A maps to NM_015027.2 Q640Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr16:15128327 G>A maps to NM_015027.2 Q640Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr18:21444831 G>A maps to ENST00000416669 P1558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr18:21444831 G>A maps to ENST00000416669 P1558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr19:11280801 G>A maps to NM_015493.6 C786C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr19:11280801 G>A maps to NM_015493.6 C786C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr19:55450491 C>G maps to ENST00000446217 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr19:55450491 C>G maps to ENST00000446217 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr2:98914448 C>T maps to NM_144992.4 S1079S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr2:98914448 C>T maps to NM_144992.4 S1079S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr21:31965095 G>A maps to NM_181605.3 *111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr21:31965095 G>A maps to NM_181605.3 *111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr4:126371854 G>C maps to NM_024582.4 V3228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr4:126371854 G>C maps to NM_024582.4 V3228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr4:187549811 G>A maps to ENST00000260147 Q1477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr4:187549811 G>A maps to ENST00000260147 Q1477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr5:14488245 G>C maps to NM_007118.2 P2503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr5:14488245 G>C maps to NM_007118.2 P2503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr5:86681170 C>T maps to NM_002890.1 Q938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr5:86681170 C>T maps to NM_002890.1 Q938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr6:26240712 C>T maps to NM_003540.3 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr6:26240712 C>T maps to NM_003540.3 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr6:44254021 C>T maps to NM_182539.3 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr6:44254021 C>T maps to NM_182539.3 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr8:9605598 G>A maps to NM_003747.2 A903A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr8:9605598 G>A maps to NM_003747.2 A903A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr8:145107417 G>A maps to ENST00000360660 N1079N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr8:145107417 G>A maps to ENST00000360660 N1079N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr9:21971027 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr9:21971027 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chrX:17744145 G>A maps to NM_198270.2 T619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chrX:17744145 G>A maps to NM_198270.2 T619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr1:9097692 C>T maps to NM_003039.2 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr1:9097692 C>T maps to NM_003039.2 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr1:9794123 C>G maps to NM_001009566.1 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr1:9794123 C>G maps to NM_001009566.1 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr1:52759158 C>T maps to NM_004799.2 F1020F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr1:52759158 C>T maps to NM_004799.2 F1020F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr1:157666064 C>G maps to NM_052939.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr1:157666064 C>G maps to NM_052939.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr1:207787830 G>T maps to NM_000651.4 E2220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr1:207787830 G>T maps to NM_000651.4 E2220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr1:231473419 C>T maps to NM_175876.3 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr1:231473419 C>T maps to NM_175876.3 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr1:247875238 A>C maps to NM_001005286.1 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr1:247875238 A>C maps to NM_001005286.1 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr10:18276457 C>T maps to NM_001145195.1 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr10:18276457 C>T maps to NM_001145195.1 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr10:38121208 C>G maps to NM_021045.1 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr10:38121208 C>G maps to NM_021045.1 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr10:73326582 C>T maps to ENST00000398860 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr10:73326582 C>T maps to ENST00000398860 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr10:98064367 C>T maps to NM_004088.3 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr10:98064367 C>T maps to NM_004088.3 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr11:294724 C>G maps to ENST00000409479 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr11:294724 C>G maps to ENST00000409479 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr11:9007291 G>A maps to NM_020645.2 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr11:9007291 G>A maps to NM_020645.2 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr11:48166646 C>G maps to NM_002843.3 S961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr11:48166646 C>G maps to NM_002843.3 S961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr11:55419206 C>T maps to NM_001004059.2 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr11:55419206 C>T maps to NM_001004059.2 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr11:65789073 C>G maps to NM_053054.3 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr11:65789073 C>G maps to NM_053054.3 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr11:68029520 G>A maps to NM_022338.3 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr11:68029520 G>A maps to NM_022338.3 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr11:82985035 C>G did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr11:82985035 C>G did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr12:11214515 C>T maps to NM_176887.2 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr12:11214515 C>T maps to NM_176887.2 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr12:46760702 C>T maps to NM_018976.4 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr12:46760702 C>T maps to NM_018976.4 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr12:50500129 C>T maps to NM_005276.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr12:50500129 C>T maps to NM_005276.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr12:53899913 C>T maps to NM_134323.1 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr12:53899913 C>T maps to NM_134323.1 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr12:57430773 C>T maps to NM_005379.2 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr12:57430773 C>T maps to NM_005379.2 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr12:111318960 G>A maps to NM_152591.1 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr12:111318960 G>A maps to NM_152591.1 Q238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr12:119568509 G>A maps to NM_194286.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr12:119568509 G>A maps to NM_194286.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr13:46092894 A>G did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr13:46092894 A>G did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr13:111919900 C>G maps to NM_001113511.1 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr13:111919900 C>G maps to NM_001113511.1 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr13:113481012 C>G maps to NM_032189.3 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr13:113481012 C>G maps to NM_032189.3 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr14:36103864 A>G maps to NM_194301.2 F1464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr14:36103864 A>G maps to NM_194301.2 F1464F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr14:60072192 G>A maps to NM_021136.2 Q669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr14:60072192 G>A maps to NM_021136.2 Q669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr14:72138363 T>C maps to NM_015556.1 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr14:72138363 T>C maps to NM_015556.1 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr14:90783140 G>C maps to NM_017970.2 S63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr14:90783140 G>C maps to NM_017970.2 S63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr15:24923323 T>A maps to NM_018958.2 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr15:24923323 T>A maps to NM_018958.2 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr15:52515860 C>T maps to NM_018728.3 L1169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr15:52515860 C>T maps to NM_018728.3 L1169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr15:53994480 G>C maps to NM_182758.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr15:53994480 G>C maps to NM_182758.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr15:62258316 G>A maps to NM_020821.2 Q1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr15:62258316 G>A maps to NM_020821.2 Q1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr15:63017194 G>C maps to NM_015059.2 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr15:63017194 G>C maps to NM_015059.2 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr15:71302303 C>T maps to NM_017691.3 F522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr15:71302303 C>T maps to NM_017691.3 F522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr15:74536423 C>T maps to ENST00000321288 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr15:74536423 C>T maps to ENST00000321288 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr16:3656526 C>T maps to NM_032444.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr16:3656526 C>T maps to NM_032444.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr16:56875738 C>T maps to NM_014669.3 R781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr16:56875738 C>T maps to NM_014669.3 R781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:3928236 C>T maps to NM_015113.3 L2356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:3928236 C>T maps to NM_015113.3 L2356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:7735023 C>G maps to NM_020877.2 V4219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:7735023 C>G maps to NM_020877.2 V4219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:16024583 C>T did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:16024583 C>T did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:18238930 A>C maps to NM_004169.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:18238930 A>C maps to NM_004169.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:37421663 G>A maps to NM_032875.2 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:37421663 G>A maps to NM_032875.2 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:49057212 G>C maps to ENST00000376407 G1102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:49057212 G>C maps to ENST00000376407 G1102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:65119121 G>C maps to NM_014877.3 V1198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:65119121 G>C maps to NM_014877.3 V1198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:78321902 G>A maps to NM_020914.4 S3305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:78321902 G>A maps to NM_020914.4 S3305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:80789424 G>C maps to NM_024702.2 Y302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr17:80789424 G>C maps to NM_024702.2 Y302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr18:346847 C>T maps to NM_130386.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr18:346847 C>T maps to NM_130386.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr18:77513777 C>T maps to NM_004715.3 N958N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr18:77513777 C>T maps to NM_004715.3 N958N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr19:1462152 C>T maps to NM_005883.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr19:1462152 C>T maps to NM_005883.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr19:3179236 G>A maps to NM_003775.3 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr19:3179236 G>A maps to NM_003775.3 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr19:12776598 C>T maps to NM_000528.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr19:12776598 C>T maps to NM_000528.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr19:12790280 C>T maps to NM_001930.2 W223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr19:12790280 C>T maps to NM_001930.2 W223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr19:53385153 C>T maps to NM_207333.2 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr19:53385153 C>T maps to NM_207333.2 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr19:55451376 G>A maps to ENST00000446217 C298C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr19:55451376 G>A maps to ENST00000446217 C298C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr19:56166481 C>T maps to NM_007279.2 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr19:56166481 C>T maps to NM_007279.2 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr2:37520322 G>C maps to NM_005813.3 S127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr2:37520322 G>C maps to NM_005813.3 S127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr2:39944276 C>T maps to NM_152390.2 C260C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr2:39944276 C>T maps to NM_152390.2 C260C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr2:69206026 C>T maps to NM_019617.3 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr2:69206026 C>T maps to NM_019617.3 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr2:86302278 G>A maps to NM_015425.3 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr2:86302278 G>A maps to NM_015425.3 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr2:100266104 G>A maps to NM_001025108.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr2:100266104 G>A maps to NM_001025108.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr2:114257405 C>T maps to NM_012184.4 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr2:114257405 C>T maps to NM_012184.4 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr2:160194091 C>T maps to NM_013450.2 R1882R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr2:160194091 C>T maps to NM_013450.2 R1882R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr20:21494271 G>A maps to NM_002509.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr20:21494271 G>A maps to NM_002509.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr20:40050615 G>C maps to NM_032221.3 L1553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr20:40050615 G>C maps to NM_032221.3 L1553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr20:47633820 T>C maps to NM_006420.2 L1451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr20:47633820 T>C maps to NM_006420.2 L1451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr21:31709899 G>T maps to NM_001077711.1 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr21:31709899 G>T maps to NM_001077711.1 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr21:43412299 C>G maps to NM_020727.4 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr21:43412299 C>G maps to NM_020727.4 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:9786776 G>C maps to NM_001003694.1 R1002R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:9786776 G>C maps to NM_001003694.1 R1002R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:11072888 T>C maps to NM_003042.3 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:11072888 T>C maps to NM_003042.3 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:14799081 C>T maps to NM_032137.4 I715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:14799081 C>T maps to NM_032137.4 I715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:18462477 G>C did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:18462477 G>C did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:49699341 C>G maps to NM_003458.3 S3355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:49699341 C>G maps to NM_003458.3 S3355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:72428558 G>A maps to ENST00000477973 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:72428558 G>A maps to ENST00000477973 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:124646818 G>C maps to NM_033049.3 S24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:124646818 G>C maps to NM_033049.3 S24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:139093346 G>A maps to NM_004766.2 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:139093346 G>A maps to NM_004766.2 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:186504983 C>G maps to ENST00000440191 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr3:186504983 C>G maps to ENST00000440191 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr4:59345 G>A maps to NM_182524.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr4:59345 G>A maps to NM_182524.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr4:6606981 G>A maps to NM_015274.1 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr4:6606981 G>A maps to NM_015274.1 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr4:57777136 G>C maps to NM_005612.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr4:57777136 G>C maps to NM_005612.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr4:100048495 C>G did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr4:100048495 C>G did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr4:187173204 A>G maps to ENST00000511608 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr4:187173204 A>G maps to ENST00000511608 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr5:192315 C>T maps to NM_001080478.1 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr5:192315 C>T maps to NM_001080478.1 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr5:132427044 T>C maps to NM_002154.3 D513D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr5:132427044 T>C maps to NM_002154.3 D513D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr6:656503 C>T maps to NM_148959.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr6:656503 C>T maps to NM_148959.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr6:7569531 C>T maps to NM_004415.2 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr6:7569531 C>T maps to NM_004415.2 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr6:24843780 G>C maps to NM_014722.2 S410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr6:24843780 G>C maps to NM_014722.2 S410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr6:83863896 A>T did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr6:83863896 A>T did not map to a codon.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr7:14027741 G>A maps to NM_004956.4 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr7:14027741 G>A maps to NM_004956.4 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr7:72849812 A>G maps to NM_003508.2 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr7:72849812 A>G maps to NM_003508.2 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr7:92195341 G>A maps to NM_152789.2 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr7:92195341 G>A maps to NM_152789.2 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr7:100686711 G>A maps to NM_001040105.1 V4005V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr7:100686711 G>A maps to NM_001040105.1 V4005V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr7:100686942 G>A maps to NM_001040105.1 T4082T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr7:100686942 G>A maps to NM_001040105.1 T4082T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr7:138602190 G>A maps to NM_001164665.1 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr7:138602190 G>A maps to NM_001164665.1 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr8:38172975 C>T maps to NM_023034.1 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr8:38172975 C>T maps to NM_023034.1 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr8:48650424 G>A maps to NM_005195.3 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr8:48650424 G>A maps to NM_005195.3 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr8:100847875 A>G maps to NM_017890.3 L3309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr8:100847875 A>G maps to NM_017890.3 L3309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr8:101733736 C>G maps to NM_002568.3 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr8:101733736 C>G maps to NM_002568.3 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr8:114031356 G>A maps to NM_198123.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr8:114031356 G>A maps to NM_198123.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr9:21971028 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr9:21971028 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr9:43628677 C>G maps to NM_001145196.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr9:43628677 C>G maps to NM_001145196.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr9:80537223 C>T maps to NM_002072.3 Q58Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr9:80537223 C>T maps to NM_002072.3 Q58Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr9:117797485 G>C maps to NM_002160.2 V1928V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr9:117797485 G>C maps to NM_002160.2 V1928V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr9:123169395 G>C maps to NM_018249.4 L1619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chr9:123169395 G>C maps to NM_018249.4 L1619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chrX:30578056 G>T maps to NM_025159.2 S139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chrX:30578056 G>T maps to NM_025159.2 S139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chrX:73964208 G>A maps to NM_001008537.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7414-01A-11D-2078-08 chrX:73964208 G>A maps to NM_001008537.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr1:7870005 G>T maps to ENST00000377532 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr1:7870005 G>T maps to ENST00000377532 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr1:12837315 G>A maps to NM_001080830.1 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr1:12837315 G>A maps to NM_001080830.1 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr1:12855676 C>G maps to NM_023013.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr1:12855676 C>G maps to NM_023013.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr1:159857774 G>T maps to NM_012337.2 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr1:159857774 G>T maps to NM_012337.2 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr1:169701063 G>A maps to NM_000450.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr1:169701063 G>A maps to NM_000450.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr1:197115444 G>C maps to NM_018136.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr1:197115444 G>C maps to NM_018136.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr10:34408629 C>T maps to NM_019619.3 S1196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr10:34408629 C>T maps to NM_019619.3 S1196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr10:87614309 G>C maps to NM_017551.2 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr10:87614309 G>C maps to NM_017551.2 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr10:88259532 C>T maps to ENST00000342368 Q574Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr10:88259532 C>T maps to ENST00000342368 Q574Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr11:6425032 G>A maps to ENST00000389906 N247N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr11:6425032 G>A maps to ENST00000389906 N247N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr12:4855414 T>C maps to NM_017417.1 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr12:4855414 T>C maps to NM_017417.1 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr12:112082287 T>C maps to NM_006768.3 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr12:112082287 T>C maps to NM_006768.3 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr13:29599503 C>T maps to NM_001033602.2 H233H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr13:29599503 C>T maps to NM_001033602.2 H233H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr13:109318468 C>T maps to NM_015011.1 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr13:109318468 C>T maps to NM_015011.1 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr16:58550235 C>T maps to NM_001160305.1 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr16:58550235 C>T maps to NM_001160305.1 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr16:71318559 T>A maps to NM_018348.5 K422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr16:71318559 T>A maps to NM_018348.5 K422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr16:88873831 C>G maps to NM_030928.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr16:88873831 C>G maps to NM_030928.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr17:6909232 G>A maps to NM_000697.2 Q435Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr17:6909232 G>A maps to NM_000697.2 Q435Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr17:9448487 C>T did not map to a codon.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr17:9448487 C>T did not map to a codon.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr18:47373591 C>T maps to NM_001080467.2 R1461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr18:47373591 C>T maps to NM_001080467.2 R1461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr19:49468782 C>T maps to NM_000146.3 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr19:49468782 C>T maps to NM_000146.3 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr2:97808555 A>G maps to NM_001164315.1 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr2:97808555 A>G maps to NM_001164315.1 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr2:183790480 C>G maps to NM_205842.1 L1118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr2:183790480 C>G maps to NM_205842.1 L1118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr21:45833912 C>G maps to ENST00000397932 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr21:45833912 C>G maps to ENST00000397932 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr3:168838958 G>A maps to NM_004991.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr3:168838958 G>A maps to NM_004991.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr3:183017858 G>A maps to NM_015078.2 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr3:183017858 G>A maps to NM_015078.2 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr4:104579370 C>T did not map to a codon.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr4:104579370 C>T did not map to a codon.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr4:163032464 A>G maps to NM_020116.3 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr4:163032464 A>G maps to NM_020116.3 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr5:127595500 C>T maps to NM_001999.3 E2795E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr5:127595500 C>T maps to NM_001999.3 E2795E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr5:140237195 G>A maps to NM_018901.2 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr5:140237195 G>A maps to NM_018901.2 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr7:107752370 G>A maps to NM_007356.2 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr7:107752370 G>A maps to NM_007356.2 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr8:110448631 G>T maps to ENST00000426474 E1191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr8:110448631 G>T maps to ENST00000426474 E1191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr9:79321540 A>G maps to NM_015225.2 Y1883Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr9:79321540 A>G maps to NM_015225.2 Y1883Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr9:123852643 G>C maps to NM_007018.4 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7415-01A-11D-2078-08 chr9:123852643 G>C maps to NM_007018.4 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr1:19487580 G>A maps to ENST00000375267 Q1746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr1:19487580 G>A maps to ENST00000375267 Q1746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr1:39341346 T>G maps to NM_030772.4 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr1:39341346 T>G maps to NM_030772.4 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr11:17793573 C>T maps to NM_001112741.1 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr11:17793573 C>T maps to NM_001112741.1 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr11:20404741 C>G maps to NM_001098520.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr11:20404741 C>G maps to NM_001098520.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr15:28517375 G>A maps to NM_004667.4 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr15:28517375 G>A maps to NM_004667.4 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr15:76496313 G>A maps to NM_152335.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr15:76496313 G>A maps to NM_152335.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr15:93016180 A>G did not map to a codon.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr15:93016180 A>G did not map to a codon.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr17:27849480 C>T maps to NM_020791.2 R698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr17:27849480 C>T maps to NM_020791.2 R698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr17:72322499 C>T maps to NM_153209.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr17:72322499 C>T maps to NM_153209.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr17:78073372 G>A maps to NM_017950.2 Q1076Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr17:78073372 G>A maps to NM_017950.2 Q1076Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr19:19231607 G>A maps to NM_017814.1 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr19:19231607 G>A maps to NM_017814.1 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr19:21607092 C>A maps to NM_001076678.2 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr19:21607092 C>A maps to NM_001076678.2 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr19:38948882 C>T maps to NM_000540.2 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr19:38948882 C>T maps to NM_000540.2 V706V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr19:52722987 G>A maps to NM_014225.5 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr19:52722987 G>A maps to NM_014225.5 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr19:56952581 C>A maps to ENST00000342634 R722R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr19:56952581 C>A maps to ENST00000342634 R722R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr19:58639325 C>T maps to NM_024620.3 Q515Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr19:58639325 C>T maps to NM_024620.3 Q515Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr2:86279994 G>A maps to NM_015425.3 T779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr2:86279994 G>A maps to NM_015425.3 T779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr2:162273104 C>T maps to NM_006593.2 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr2:162273104 C>T maps to NM_006593.2 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr2:219000420 C>T maps to NM_001168298.1 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr2:219000420 C>T maps to NM_001168298.1 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr21:46899994 G>A maps to ENST00000359759 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr21:46899994 G>A maps to ENST00000359759 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr3:50402369 C>T maps to ENST00000435965 Q1090Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr3:50402369 C>T maps to ENST00000435965 Q1090Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr3:108117635 C>A maps to NM_014981.1 E1681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr3:108117635 C>A maps to NM_014981.1 E1681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr4:100543977 G>A maps to ENST00000511045 P913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr4:100543977 G>A maps to ENST00000511045 P913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr5:33937015 G>A maps to NM_016568.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr5:33937015 G>A maps to NM_016568.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr8:110441661 C>T maps to ENST00000426474 L1032L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr8:110441661 C>T maps to ENST00000426474 L1032L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr9:135553692 G>A maps to NM_012204.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr9:135553692 G>A maps to NM_012204.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chrX:24745917 C>G maps to ENST00000379068 V517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chrX:24745917 C>G maps to ENST00000379068 V517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chrX:64196324 C>T did not map to a codon.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chrX:64196324 C>T did not map to a codon.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chrX:79960223 T>A maps to NM_153252.4 K892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chrX:79960223 T>A maps to NM_153252.4 K892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chrX:104463740 C>T maps to NM_031274.3 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chrX:104463740 C>T maps to NM_031274.3 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chrX:140995292 A>T maps to NM_005462.4 G701G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chrX:140995292 A>T maps to NM_005462.4 G701G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr1:16046239 C>T maps to ENST00000420314 Y262Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr1:16046239 C>T maps to ENST00000420314 Y262Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr1:236205525 G>A maps to NM_002508.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr1:236205525 G>A maps to NM_002508.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr1:248367253 G>A maps to NM_001004689.1 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr1:248367253 G>A maps to NM_001004689.1 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr10:74234890 C>T maps to NM_006077.3 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr10:74234890 C>T maps to NM_006077.3 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr10:105174032 T>C maps to NM_014976.1 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr10:105174032 T>C maps to NM_014976.1 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr11:1862047 G>A did not map to a codon.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr11:1862047 G>A did not map to a codon.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr11:65144111 T>A maps to NM_182556.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr11:65144111 T>A maps to NM_182556.2 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr11:66083526 C>T maps to NM_020404.2 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr11:66083526 C>T maps to NM_020404.2 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr11:66083844 C>T maps to NM_020404.2 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr11:66083844 C>T maps to NM_020404.2 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr11:122930646 C>T maps to NM_006597.3 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr11:122930646 C>T maps to NM_006597.3 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr12:3921419 G>A maps to NM_020367.4 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr12:3921419 G>A maps to NM_020367.4 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr12:113906036 C>T maps to NM_022363.2 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr12:113906036 C>T maps to NM_022363.2 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr13:31711646 T>C maps to NM_006644.2 T795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr13:31711646 T>C maps to NM_006644.2 T795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr13:49796404 G>A maps to NM_001507.1 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr13:49796404 G>A maps to NM_001507.1 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr14:20837658 G>A maps to NM_007110.4 T2500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr14:20837658 G>A maps to NM_007110.4 T2500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr14:23450640 C>A maps to NM_032876.4 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr14:23450640 C>A maps to NM_032876.4 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr14:61180763 C>T maps to NM_017420.4 Q569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr14:61180763 C>T maps to NM_017420.4 Q569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr14:69704289 A>G did not map to a codon.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr14:69704289 A>G did not map to a codon.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr15:43102901 G>A maps to ENST00000263802 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr15:43102901 G>A maps to ENST00000263802 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr16:27765492 G>A did not map to a codon.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr16:27765492 G>A did not map to a codon.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr16:67234108 G>A maps to NM_024712.3 E139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr16:67234108 G>A maps to NM_024712.3 E139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr17:2290452 G>C maps to NM_020310.2 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr17:2290452 G>C maps to NM_020310.2 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr17:17120409 G>A maps to NM_144997.5 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr17:17120409 G>A maps to NM_144997.5 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr17:28537589 C>T maps to ENST00000394821 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr17:28537589 C>T maps to ENST00000394821 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr17:37899469 G>T maps to ENST00000445327 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr17:37899469 G>T maps to ENST00000445327 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr17:65186377 T>G maps to NM_014877.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr17:65186377 T>G maps to NM_014877.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr17:72929558 C>T maps to NM_178160.2 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr17:72929558 C>T maps to NM_178160.2 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr18:25589800 C>A maps to NM_001792.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr18:25589800 C>A maps to NM_001792.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr19:4432044 C>T maps to NM_005483.2 Q682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr19:4432044 C>T maps to NM_005483.2 Q682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr19:9361988 T>G maps to NM_001079935.1 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr19:9361988 T>G maps to NM_001079935.1 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr19:55805722 A>C maps to NM_032430.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr19:55805722 A>C maps to NM_032430.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr2:169989167 A>G maps to NM_004525.2 D4548D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr2:169989167 A>G maps to NM_004525.2 D4548D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr20:23545617 G>C maps to NM_080610.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr20:23545617 G>C maps to NM_080610.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr20:34090745 C>A maps to NM_007186.3 R1517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr20:34090745 C>A maps to NM_007186.3 R1517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr22:36701123 G>T maps to NM_002473.4 S728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr22:36701123 G>T maps to NM_002473.4 S728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr22:42482285 T>C maps to NM_002490.3 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr22:42482285 T>C maps to NM_002490.3 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr3:48694602 G>A maps to NM_001407.2 D1309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr3:48694602 G>A maps to NM_001407.2 D1309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr3:125172709 T>C maps to NM_003794.2 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr3:125172709 T>C maps to NM_003794.2 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr3:139092254 C>A did not map to a codon.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr3:139092254 C>A did not map to a codon.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr3:155551698 T>C maps to NM_004733.3 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr3:155551698 T>C maps to NM_004733.3 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr5:137426395 C>T maps to NM_058244.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr5:137426395 C>T maps to NM_058244.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr6:75851808 G>A maps to ENST00000322507 V1632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr6:75851808 G>A maps to ENST00000322507 V1632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr7:44801093 T>C maps to NM_031449.3 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr7:44801093 T>C maps to NM_031449.3 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr7:63679785 A>G maps to NM_001159524.1 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr7:63679785 A>G maps to NM_001159524.1 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr7:96747112 C>T maps to NM_020186.2 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr7:96747112 C>T maps to NM_020186.2 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr7:99091988 A>G maps to NM_032164.2 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr7:99091988 A>G maps to NM_032164.2 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr7:139727185 G>T maps to NM_022750.2 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr7:139727185 G>T maps to NM_022750.2 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr8:70517084 C>G maps to NM_001128206.1 S432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr8:70517084 C>G maps to NM_001128206.1 S432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr8:100880544 G>A maps to NM_017890.3 P3773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr8:100880544 G>A maps to NM_017890.3 P3773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr8:113585823 G>A maps to NM_198123.1 R1316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr8:113585823 G>A maps to NM_198123.1 R1316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr8:126061385 G>A maps to ENST00000377985 T752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr8:126061385 G>A maps to ENST00000377985 T752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr8:145151331 T>C maps to NM_001916.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr8:145151331 T>C maps to NM_001916.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr9:35107863 C>T maps to NM_025182.2 W136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr9:35107863 C>T maps to NM_025182.2 W136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chrX:48780922 G>T maps to NM_017602.3 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chrX:48780922 G>T maps to NM_017602.3 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr15:89876484 C>T maps to NM_002693.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7418-01A-11D-2078-08 chr15:89876484 C>T maps to NM_002693.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr10:72636949 A>G did not map to a codon.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr10:72636949 A>G did not map to a codon.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr11:47464318 G>C maps to NM_005055.3 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr11:47464318 G>C maps to NM_005055.3 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr11:121384940 C>T maps to NM_003105.5 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr11:121384940 C>T maps to NM_003105.5 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr12:6646507 C>T maps to NM_002046.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr12:6646507 C>T maps to NM_002046.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr12:53516947 C>T maps to NM_003578.3 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr12:53516947 C>T maps to NM_003578.3 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr12:57351083 G>T maps to NM_003708.3 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr12:57351083 G>T maps to NM_003708.3 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr14:102502846 C>A maps to NM_001376.4 P3592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr14:102502846 C>A maps to NM_001376.4 P3592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr15:83710627 A>G maps to NM_025238.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr15:83710627 A>G maps to NM_025238.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr16:24801105 A>G maps to NM_014494.2 K381K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr16:24801105 A>G maps to NM_014494.2 K381K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr16:50063657 C>G maps to NM_153261.4 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr16:50063657 C>G maps to NM_153261.4 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr17:38508321 G>A maps to NM_001145301.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr17:38508321 G>A maps to NM_001145301.2 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr17:67020424 G>T maps to NM_080283.3 A737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr17:67020424 G>T maps to NM_080283.3 A737A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr18:73000484 C>T maps to NM_005786.4 L996L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr18:73000484 C>T maps to NM_005786.4 L996L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr19:12856228 C>T maps to NM_004317.2 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr19:12856228 C>T maps to NM_004317.2 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr19:19338828 G>C maps to NM_004386.2 G800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr19:19338828 G>C maps to NM_004386.2 G800G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr19:54395867 G>A maps to NM_002739.3 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr19:54395867 G>A maps to NM_002739.3 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr2:11347877 C>T maps to NM_004850.3 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr2:11347877 C>T maps to NM_004850.3 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr2:37347200 G>A maps to NM_001135651.1 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr2:37347200 G>A maps to NM_001135651.1 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr20:6031558 C>T maps to NM_152611.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr20:6031558 C>T maps to NM_152611.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr20:30154065 G>A maps to NM_178581.1 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr20:30154065 G>A maps to NM_178581.1 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr21:27840861 C>T maps to ENST00000435845 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr21:27840861 C>T maps to ENST00000435845 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr21:34923612 T>A maps to NM_138927.1 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr21:34923612 T>A maps to NM_138927.1 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr4:87692490 G>A maps to NM_080685.2 G1662G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr4:87692490 G>A maps to NM_080685.2 G1662G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr4:120243206 C>T maps to NM_000134.3 K17K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr4:120243206 C>T maps to NM_000134.3 K17K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr5:1422041 G>C maps to NM_001044.4 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr5:1422041 G>C maps to NM_001044.4 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr6:34826613 C>T maps to NM_017754.3 R827R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr6:34826613 C>T maps to NM_017754.3 R827R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr7:30113747 G>T maps to ENST00000440706 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr7:30113747 G>T maps to ENST00000440706 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr7:99703603 C>T maps to ENST00000429084 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr7:99703603 C>T maps to ENST00000429084 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr8:42587133 C>G maps to NM_000749.3 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr8:42587133 C>G maps to NM_000749.3 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr8:42587172 C>A maps to NM_000749.3 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr8:42587172 C>A maps to NM_000749.3 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr8:144658292 G>A maps to ENST00000276844 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr8:144658292 G>A maps to ENST00000276844 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr9:114911524 T>A maps to NM_022486.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr9:114911524 T>A maps to NM_022486.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr9:123239728 C>T did not map to a codon.
Sequencing variant TCGA-CV-7421-01A-11D-2078-08 chr9:123239728 C>T did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr1:10132156 C>A maps to NM_001105562.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr1:10132156 C>A maps to NM_001105562.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr1:27106227 C>T maps to NM_006015.4 Q1947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr1:27106227 C>T maps to NM_006015.4 Q1947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr1:57415425 C>A did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr1:57415425 C>A did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr1:152327954 G>A maps to NM_001014342.2 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr1:152327954 G>A maps to NM_001014342.2 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr1:154523417 T>C maps to NM_017582.6 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr1:154523417 T>C maps to NM_017582.6 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr1:186909194 C>T maps to NM_024420.2 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr1:186909194 C>T maps to NM_024420.2 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr10:5958322 T>C maps to NM_032807.3 F615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr10:5958322 T>C maps to NM_032807.3 F615F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr10:30315989 C>G maps to NM_020848.2 G1029G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr10:30315989 C>G maps to NM_020848.2 G1029G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr10:60461889 C>A maps to NM_001080512.1 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr10:60461889 C>A maps to NM_001080512.1 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr10:90707104 C>G maps to NM_001141945.1 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr10:90707104 C>G maps to NM_001141945.1 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr10:101090474 C>G maps to NM_020348.2 S444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr10:101090474 C>G maps to NM_020348.2 S444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr11:14989342 T>G maps to NM_001033953.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr11:14989342 T>G maps to NM_001033953.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr11:66191815 G>A maps to NM_178864.3 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr11:66191815 G>A maps to NM_178864.3 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr11:70224266 C>T maps to NM_003626.2 S1172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr11:70224266 C>T maps to NM_003626.2 S1172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr11:128354826 C>G maps to NM_001143820.1 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr11:128354826 C>G maps to NM_001143820.1 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr12:49443616 G>A maps to NM_003482.3 R1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr12:49443616 G>A maps to NM_003482.3 R1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr12:57619421 C>A maps to NM_007224.3 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr12:57619421 C>A maps to NM_007224.3 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr12:72020215 C>A maps to NM_144982.4 E1381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr12:72020215 C>A maps to NM_144982.4 E1381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr12:78400889 C>G maps to NM_014903.4 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr12:78400889 C>G maps to NM_014903.4 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr12:112681212 G>A maps to NM_001109662.2 V1462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr12:112681212 G>A maps to NM_001109662.2 V1462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr12:125398023 G>A maps to NM_021009.5 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr12:125398023 G>A maps to NM_021009.5 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr15:22990178 G>C maps to NM_014608.2 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr15:22990178 G>C maps to NM_014608.2 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr15:34040340 G>T maps to NM_001036.3 A2672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr15:34040340 G>T maps to NM_001036.3 A2672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr15:39544746 T>G maps to NM_207445.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr15:39544746 T>G maps to NM_207445.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr15:85401043 G>A maps to NM_020778.4 Q1227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr15:85401043 G>A maps to NM_020778.4 Q1227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr16:31419084 A>T maps to ENST00000316569 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr16:31419084 A>T maps to ENST00000316569 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr16:56865769 G>T maps to NM_014669.3 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr16:56865769 G>T maps to NM_014669.3 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr17:7579376 G>A maps to NM_001126112.1 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr17:7579376 G>A maps to NM_001126112.1 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr17:10399766 C>A maps to NM_005963.3 E1586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr17:10399766 C>A maps to NM_005963.3 E1586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr17:39577791 G>A maps to NM_003770.4 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr17:39577791 G>A maps to NM_003770.4 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr17:45235605 G>A maps to NM_001114091.1 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr17:45235605 G>A maps to NM_001114091.1 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr17:66268876 A>G maps to NM_004694.4 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr17:66268876 A>G maps to NM_004694.4 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr19:16006373 G>T maps to NM_001082.3 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr19:16006373 G>T maps to NM_001082.3 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr2:98411467 A>C maps to NM_015348.1 L1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr2:98411467 A>C maps to NM_015348.1 L1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr2:109463282 G>A maps to NM_144978.1 Q471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr2:109463282 G>A maps to NM_144978.1 Q471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr2:179592513 T>C maps to NM_133378.4 L5353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr2:179592513 T>C maps to NM_133378.4 L5353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr2:219610492 C>T maps to NM_014640.4 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr2:219610492 C>T maps to NM_014640.4 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr20:36975002 C>T maps to NM_004139.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr20:36975002 C>T maps to NM_004139.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr22:38165091 G>A maps to NM_001039141.2 Q2211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr22:38165091 G>A maps to NM_001039141.2 Q2211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr3:14965560 G>A maps to NM_152536.3 S1328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr3:14965560 G>A maps to NM_152536.3 S1328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr3:88040985 C>T maps to NM_000866.3 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr3:88040985 C>T maps to NM_000866.3 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr3:192516359 G>A maps to NM_178496.3 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr3:192516359 G>A maps to NM_178496.3 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr4:30723145 C>G maps to NM_001173523.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr4:30723145 C>G maps to NM_001173523.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr4:72620733 G>A maps to ENST00000504199 C394C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr4:72620733 G>A maps to ENST00000504199 C394C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr4:187208887 G>T maps to NM_000128.3 E543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr4:187208887 G>T maps to NM_000128.3 E543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr5:195404 C>T maps to NM_001080478.1 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr5:195404 C>T maps to NM_001080478.1 F494F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr5:75906863 C>T maps to NM_006633.2 Y459Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr5:75906863 C>T maps to NM_006633.2 Y459Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr6:26392972 G>A maps to NM_001197237.1 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr6:26392972 G>A maps to NM_001197237.1 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr6:83834482 T>A maps to NM_015018.2 L467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr6:83834482 T>A maps to NM_015018.2 L467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr6:116938022 A>G maps to NM_001010892.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr6:116938022 A>G maps to NM_001010892.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr6:152631903 T>C maps to NM_182961.2 Q5605Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr6:152631903 T>C maps to NM_182961.2 Q5605Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr7:122787223 C>T maps to NM_022444.3 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr7:122787223 C>T maps to NM_022444.3 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr9:90500808 A>C maps to NM_178828.4 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr9:90500808 A>C maps to NM_178828.4 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr9:125486387 G>A maps to NM_001005235.1 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chr9:125486387 G>A maps to NM_001005235.1 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chrX:19039219 A>G did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chrX:19039219 A>G did not map to a codon.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chrX:54492143 G>T maps to NM_004463.2 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chrX:54492143 G>T maps to NM_004463.2 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chrX:70347859 C>G maps to ENST00000333646 T1033T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chrX:70347859 C>G maps to ENST00000333646 T1033T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chrX:119672527 G>T maps to NM_003588.3 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7422-01A-21D-2078-08 chrX:119672527 G>T maps to NM_003588.3 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:39878081 T>C maps to NM_015038.1 C715C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:39878081 T>C maps to NM_015038.1 C715C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:94496610 G>A maps to NM_000350.2 G1398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:94496610 G>A maps to NM_000350.2 G1398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:110456909 C>T maps to NM_000757.4 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:110456909 C>T maps to NM_000757.4 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:114354935 C>T maps to NM_018364.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:114354935 C>T maps to NM_018364.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:150967078 G>A maps to NM_003568.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:150967078 G>A maps to NM_003568.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:236180535 C>T maps to NM_002508.2 G722G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:236180535 C>T maps to NM_002508.2 G722G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:240071197 C>A maps to NM_000740.2 Y149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:240071197 C>A maps to NM_000740.2 Y149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:240492665 C>A maps to ENST00000406993 P1588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr1:240492665 C>A maps to ENST00000406993 P1588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr11:8123159 C>T maps to NM_003320.4 C560C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr11:8123159 C>T maps to NM_003320.4 C560C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr11:60170535 T>C did not map to a codon.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr11:60170535 T>C did not map to a codon.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr11:67172898 G>A maps to NM_198517.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr11:67172898 G>A maps to NM_198517.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr11:68822186 A>G did not map to a codon.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr11:68822186 A>G did not map to a codon.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr12:44148847 A>G maps to NM_031292.3 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr12:44148847 A>G maps to NM_031292.3 F67F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr14:23847949 C>T maps to ENST00000339180 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr14:23847949 C>T maps to ENST00000339180 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr15:43545011 G>C maps to NM_201631.3 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr15:43545011 G>C maps to NM_201631.3 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr15:57730853 C>T maps to NM_032866.3 C219C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr15:57730853 C>T maps to NM_032866.3 C219C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr15:59064130 C>T maps to NM_001040450.1 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr15:59064130 C>T maps to NM_001040450.1 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr15:74740854 C>T maps to NM_201265.1 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr15:74740854 C>T maps to NM_201265.1 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr16:2158546 G>A maps to NM_001009944.2 P2207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr16:2158546 G>A maps to NM_001009944.2 P2207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr19:46094974 G>A maps to NM_005282.2 N50N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr19:46094974 G>A maps to NM_005282.2 N50N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr20:13279971 C>T maps to NM_080826.1 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr20:13279971 C>T maps to NM_080826.1 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr20:56137827 G>A maps to NM_002591.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr20:56137827 G>A maps to NM_002591.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr20:62192985 G>A maps to NM_001037335.2 S2268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr20:62192985 G>A maps to NM_001037335.2 S2268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr22:17619606 C>A maps to NM_033070.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr22:17619606 C>A maps to NM_033070.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr22:32017675 G>A maps to ENST00000422296 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr22:32017675 G>A maps to ENST00000422296 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr22:38823813 C>T maps to NM_152868.1 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr22:38823813 C>T maps to NM_152868.1 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr22:41752803 C>G maps to ENST00000351589 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr22:41752803 C>G maps to ENST00000351589 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr5:140215473 C>T maps to NM_018910.2 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr5:140215473 C>T maps to NM_018910.2 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr6:38704880 C>G maps to ENST00000327475 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr6:38704880 C>G maps to ENST00000327475 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr6:74331547 G>A maps to NM_012434.4 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr6:74331547 G>A maps to NM_012434.4 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr7:73474264 T>A maps to ENST00000358929 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr7:73474264 T>A maps to ENST00000358929 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr7:73474270 T>C maps to ENST00000358929 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr7:73474270 T>C maps to ENST00000358929 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr7:100246280 G>A maps to NM_016188.4 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr7:100246280 G>A maps to NM_016188.4 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr7:100678876 G>T maps to NM_001040105.1 G1394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr7:100678876 G>T maps to NM_001040105.1 G1394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr7:110303747 G>A maps to NM_032549.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr7:110303747 G>A maps to NM_032549.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr8:101149816 G>A maps to NM_001029860.3 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr8:101149816 G>A maps to NM_001029860.3 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr9:89771558 T>C maps to NM_001001709.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr9:89771558 T>C maps to NM_001001709.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chrX:86877395 C>A maps to NM_057162.2 Y370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chrX:86877395 C>A maps to NM_057162.2 Y370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr5:3600114 G>A maps to NM_024337.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7423-01A-11D-2078-08 chr5:3600114 G>A maps to NM_024337.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr1:79357298 G>A maps to NM_022159.3 H640H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr1:79357298 G>A maps to NM_022159.3 H640H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr1:172356475 C>T maps to ENST00000359070 D764D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr1:172356475 C>T maps to ENST00000359070 D764D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr1:192321330 T>C maps to NM_001039152.3 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr1:192321330 T>C maps to NM_001039152.3 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr1:237664038 A>G maps to NM_001035.2 P744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr1:237664038 A>G maps to NM_001035.2 P744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr1:248525601 C>A maps to NM_001004696.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr1:248525601 C>A maps to NM_001004696.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr10:26581497 G>A maps to NM_001134366.1 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr10:26581497 G>A maps to NM_001134366.1 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr10:37431033 T>G maps to ENST00000374660 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr10:37431033 T>G maps to ENST00000374660 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr10:45799762 C>T maps to NM_001004297.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr10:45799762 C>T maps to NM_001004297.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr10:50946287 C>T maps to NM_018245.2 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr10:50946287 C>T maps to NM_018245.2 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr11:56185141 G>A maps to NM_001004744.1 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr11:56185141 G>A maps to NM_001004744.1 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr11:63517598 C>T maps to ENST00000377819 V889V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr11:63517598 C>T maps to ENST00000377819 V889V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr11:85456723 G>A maps to NM_001162953.1 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr11:85456723 G>A maps to NM_001162953.1 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr12:4479715 G>A maps to NM_020638.2 D183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr12:4479715 G>A maps to NM_020638.2 D183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr12:50471783 C>T maps to NM_020039.2 D237D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr12:50471783 C>T maps to NM_020039.2 D237D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr13:24868930 G>A maps to ENST00000424834 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr13:24868930 G>A maps to ENST00000424834 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr14:92491670 G>A maps to NM_004239.3 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr14:92491670 G>A maps to NM_004239.3 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr14:105416846 G>A maps to NM_138420.2 A1647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr14:105416846 G>A maps to NM_138420.2 A1647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr15:96880845 C>T maps to NM_021005.3 Q414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr15:96880845 C>T maps to NM_021005.3 Q414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr16:16170204 C>T maps to ENST00000399408 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr16:16170204 C>T maps to ENST00000399408 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr16:61687978 G>T maps to NM_001796.2 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr16:61687978 G>T maps to NM_001796.2 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr17:10412810 G>C maps to NM_005963.3 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr17:10412810 G>C maps to NM_005963.3 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr17:10608830 G>A maps to NM_020233.4 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr17:10608830 G>A maps to NM_020233.4 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr17:41276071 G>A maps to ENST00000471181 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr17:41276071 G>A maps to ENST00000471181 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr17:72860033 C>A maps to ENST00000442102 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr17:72860033 C>A maps to ENST00000442102 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr17:74392379 C>A maps to NM_022066.3 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr17:74392379 C>A maps to NM_022066.3 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr18:22804523 G>A maps to NM_015461.2 Q1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr18:22804523 G>A maps to NM_015461.2 Q1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:7754153 C>A maps to NM_002002.4 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:7754153 C>A maps to NM_002002.4 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:9065155 T>C maps to NM_024690.2 Q7430Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:9065155 T>C maps to NM_024690.2 Q7430Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:11727527 C>T maps to NM_145295.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:11727527 C>T maps to NM_145295.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:37880678 C>T maps to NM_032453.1 H576H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:37880678 C>T maps to NM_032453.1 H576H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:47844439 C>G maps to NM_018485.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:47844439 C>G maps to NM_018485.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:53058460 G>A maps to NM_001039886.3 K764K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:53058460 G>A maps to NM_001039886.3 K764K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:57175081 C>T maps to NM_001005850.1 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:57175081 C>T maps to NM_001005850.1 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr2:1805524 C>T maps to ENST00000399161 K1073K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr2:1805524 C>T maps to ENST00000399161 K1073K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr2:21224688 G>T maps to NM_000384.2 I4535I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr2:21224688 G>T maps to NM_000384.2 I4535I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr2:27016145 G>A maps to NM_001809.3 *141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr2:27016145 G>A maps to NM_001809.3 *141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr2:31572646 C>T maps to NM_000379.3 Q958Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr2:31572646 C>T maps to NM_000379.3 Q958Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr2:74652066 A>T maps to NM_032118.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr2:74652066 A>T maps to NM_032118.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr2:172926265 C>T maps to NM_199227.1 Y27Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr2:172926265 C>T maps to NM_199227.1 Y27Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr2:242650890 C>T maps to NM_032329.4 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr2:242650890 C>T maps to NM_032329.4 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr21:41142936 C>T maps to NM_001080444.1 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr21:41142936 C>T maps to NM_001080444.1 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr22:31740835 G>A maps to NM_014323.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr22:31740835 G>A maps to NM_014323.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr3:143082404 C>A maps to NM_173653.3 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr3:143082404 C>A maps to NM_173653.3 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr3:145809655 G>T maps to NM_182943.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr3:145809655 G>T maps to NM_182943.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr3:164773032 T>G maps to NM_001041.3 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr3:164773032 T>G maps to NM_001041.3 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr3:184295734 C>T maps to NM_004443.3 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr3:184295734 C>T maps to NM_004443.3 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr4:13545813 G>A maps to NM_001189.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr4:13545813 G>A maps to NM_001189.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr4:102984275 A>G maps to NM_017935.4 P731P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr4:102984275 A>G maps to NM_017935.4 P731P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr4:129886440 C>T maps to NM_144643.2 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr4:129886440 C>T maps to NM_144643.2 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr5:6749697 C>T maps to NM_006999.4 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr5:6749697 C>T maps to NM_006999.4 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr5:13737359 C>A did not map to a codon.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr5:13737359 C>A did not map to a codon.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr5:34863072 G>A maps to NM_144725.3 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr5:34863072 G>A maps to NM_144725.3 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr5:140250370 G>A maps to NM_018902.3 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr5:140250370 G>A maps to NM_018902.3 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr6:29012394 C>T maps to NM_030903.3 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr6:29012394 C>T maps to NM_030903.3 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr6:50011491 G>A maps to NM_001037498.1 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr6:50011491 G>A maps to NM_001037498.1 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr6:112671569 T>C maps to NM_001013734.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr6:112671569 T>C maps to NM_001013734.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr7:99711748 G>A maps to ENST00000472509 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr7:99711748 G>A maps to ENST00000472509 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr7:126173488 G>A maps to NM_001127323.1 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr7:126173488 G>A maps to NM_001127323.1 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr8:381401 A>T maps to NM_183421.1 K66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr8:381401 A>T maps to NM_183421.1 K66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr8:23179756 T>G maps to NM_002318.2 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr8:23179756 T>G maps to NM_002318.2 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr8:71069393 G>A maps to NM_006540.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr8:71069393 G>A maps to NM_006540.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr8:139696688 G>A maps to NM_152888.1 L997L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr8:139696688 G>A maps to NM_152888.1 L997L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr9:21971185 G>A maps to NM_001195132.1 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr9:98242783 C>T maps to NM_000264.3 W278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr9:98242783 C>T maps to NM_000264.3 W278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr9:108110641 C>G maps to NM_080546.3 S137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr9:108110641 C>G maps to NM_080546.3 S137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr9:139405240 G>A maps to NM_017617.3 V868V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr9:139405240 G>A maps to NM_017617.3 V868V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chrX:27766112 G>T maps to NM_001136533.1 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chrX:27766112 G>T maps to NM_001136533.1 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chrX:32305681 C>T maps to ENST00000357033 W2085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chrX:32305681 C>T maps to ENST00000357033 W2085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chrX:74494188 C>T maps to NM_145052.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chrX:74494188 C>T maps to NM_145052.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr1:27102149 C>T maps to NM_006015.4 N1692N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr1:27102149 C>T maps to NM_006015.4 N1692N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr1:72400875 T>G maps to NM_173808.2 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr1:72400875 T>G maps to NM_173808.2 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr1:179544753 C>T maps to NM_014625.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr1:179544753 C>T maps to NM_014625.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr1:183192456 C>T maps to NM_005562.2 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr1:183192456 C>T maps to NM_005562.2 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr11:65732030 C>T maps to NM_005146.4 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr11:65732030 C>T maps to NM_005146.4 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr11:92715441 C>T maps to NM_005959.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr11:92715441 C>T maps to NM_005959.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr11:124489329 C>A maps to NM_052959.2 Y226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr11:124489329 C>A maps to NM_052959.2 Y226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr12:50369452 G>A maps to NM_001652.3 *283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr12:50369452 G>A maps to NM_001652.3 *283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr15:67571826 C>T maps to NM_001031715.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr15:67571826 C>T maps to NM_001031715.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr15:93563369 C>T maps to NM_001271.3 R1679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr15:93563369 C>T maps to NM_001271.3 R1679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr16:815613 G>A maps to NM_013404.4 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr16:815613 G>A maps to NM_013404.4 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr17:10363394 C>T maps to NM_017533.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr17:10363394 C>T maps to NM_017533.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr17:33507655 G>A maps to NM_173167.2 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr17:33507655 G>A maps to NM_173167.2 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr18:6311561 G>A maps to NM_173464.3 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr18:6311561 G>A maps to NM_173464.3 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr19:30935482 C>A maps to NM_014717.1 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr19:30935482 C>A maps to NM_014717.1 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr19:33623311 G>A maps to NM_173479.3 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr19:33623311 G>A maps to NM_173479.3 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr19:36048662 G>T maps to NM_000704.2 C529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr19:36048662 G>T maps to NM_000704.2 C529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr19:49564711 G>A maps to NM_006179.4 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr19:49564711 G>A maps to NM_006179.4 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr19:52443550 C>T maps to NM_001031721.3 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr19:52443550 C>T maps to NM_001031721.3 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr19:55087310 G>T maps to NM_001130917.1 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr19:55087310 G>T maps to NM_001130917.1 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr2:55570924 G>A maps to ENST00000436346 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr2:55570924 G>A maps to ENST00000436346 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr2:179467096 C>T maps to NM_133378.4 K15776K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr2:179467096 C>T maps to NM_133378.4 K15776K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr2:191116989 G>A maps to NM_014362.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr2:191116989 G>A maps to NM_014362.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr2:196726484 G>C maps to NM_018897.2 L2564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr2:196726484 G>C maps to NM_018897.2 L2564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr2:202150029 C>T maps to NM_001080125.1 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr2:202150029 C>T maps to NM_001080125.1 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr2:239237416 T>C maps to NM_015650.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr2:239237416 T>C maps to NM_015650.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr20:3211198 G>A maps to NM_001174090.1 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr20:3211198 G>A maps to NM_001174090.1 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr20:5948560 G>A maps to NM_032485.4 K371K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr20:5948560 G>A maps to NM_032485.4 K371K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr21:46320234 G>A maps to NM_000211.3 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr21:46320234 G>A maps to NM_000211.3 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr22:22890815 G>A maps to NM_206954.1 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr22:22890815 G>A maps to NM_206954.1 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr3:48476324 G>A maps to NM_024661.3 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr3:48476324 G>A maps to NM_024661.3 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr3:48617462 C>A did not map to a codon.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr3:48617462 C>A did not map to a codon.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr3:118865965 G>C maps to NM_152539.2 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr3:118865965 G>C maps to NM_152539.2 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr4:40339348 C>T maps to NM_017581.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr4:40339348 C>T maps to NM_017581.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr5:41382583 A>G maps to NM_001005473.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr5:41382583 A>G maps to NM_001005473.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr5:140181873 A>T maps to NM_018906.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr5:140181873 A>T maps to NM_018906.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr5:140558773 C>T maps to NM_019120.2 Q387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr5:140558773 C>T maps to NM_019120.2 Q387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr6:31239381 C>A maps to ENST00000383329 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr6:31239381 C>A maps to ENST00000383329 E113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr6:99283615 G>A maps to NM_005604.2 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr6:99283615 G>A maps to NM_005604.2 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr6:158449944 C>G maps to NM_003898.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr6:158449944 C>G maps to NM_003898.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr7:14758227 C>T maps to NM_004080.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr7:14758227 C>T maps to NM_004080.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr7:88963051 C>G maps to NM_181646.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr7:88963051 C>G maps to NM_181646.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr8:71071825 A>G maps to NM_006540.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr8:71071825 A>G maps to NM_006540.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr8:95866049 C>G maps to NM_017864.2 V553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr8:95866049 C>G maps to NM_017864.2 V553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr8:103317372 A>G maps to NM_015902.4 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr8:103317372 A>G maps to NM_015902.4 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr9:14674242 G>T maps to NM_178566.4 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr9:14674242 G>T maps to NM_178566.4 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr9:139994164 C>T maps to NM_016219.3 Q250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr9:139994164 C>T maps to NM_016219.3 Q250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chrX:53613474 G>C maps to ENST00000276009 S1600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chrX:53613474 G>C maps to ENST00000276009 S1600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chrX:55513553 G>A maps to NM_201286.3 R607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chrX:55513553 G>A maps to NM_201286.3 R607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chrX:74742781 G>A maps to NM_144969.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chrX:74742781 G>A maps to NM_144969.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chrX:129149171 G>A maps to ENST00000303743 T808T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chrX:129149171 G>A maps to ENST00000303743 T808T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr11:113803664 C>T maps to NM_006028.3 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7425-01A-11D-2078-08 chr11:113803664 C>T maps to NM_006028.3 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:1147456 C>A maps to NM_003327.3 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:1147456 C>A maps to NM_003327.3 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:9795144 C>G maps to NM_001009566.1 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:9795144 C>G maps to NM_001009566.1 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:12837642 C>T maps to NM_001080830.1 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:12837642 C>T maps to NM_001080830.1 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:20474785 C>T maps to NM_022819.3 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:20474785 C>T maps to NM_022819.3 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:27942092 C>T maps to NM_005248.2 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:27942092 C>T maps to NM_005248.2 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:28793130 C>T maps to NM_023923.3 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:28793130 C>T maps to NM_023923.3 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:44069507 G>A maps to NM_002840.3 K895K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:44069507 G>A maps to NM_002840.3 K895K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:44456111 C>A maps to ENST00000309519 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:44456111 C>A maps to ENST00000309519 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:62703987 C>T maps to NM_181712.4 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:62703987 C>T maps to NM_181712.4 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:67236138 G>A maps to NM_152665.2 Q63Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:67236138 G>A maps to NM_152665.2 Q63Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:155030887 C>T maps to NM_207197.1 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:155030887 C>T maps to NM_207197.1 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:158641185 G>A maps to NM_003126.2 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:158641185 G>A maps to NM_003126.2 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:160281695 G>A maps to NM_001098398.1 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:160281695 G>A maps to NM_001098398.1 F346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:169761756 C>T maps to NM_033418.1 K360K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:169761756 C>T maps to NM_033418.1 K360K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:175299263 C>A maps to NM_003285.2 E1247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:175299263 C>A maps to NM_003285.2 E1247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:207643211 G>A maps to NM_001006658.2 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr1:207643211 G>A maps to NM_001006658.2 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr10:70156606 G>A maps to NM_017987.4 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr10:70156606 G>A maps to NM_017987.4 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr10:99527327 G>A maps to NM_003015.3 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr10:99527327 G>A maps to NM_003015.3 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr10:104173809 G>A maps to NM_002779.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr10:104173809 G>A maps to NM_002779.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:1016424 G>A maps to NM_005961.2 Q2126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:1016424 G>A maps to NM_005961.2 Q2126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:32417878 G>A maps to NM_024426.4 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:32417878 G>A maps to NM_024426.4 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:62286411 C>G maps to NM_001620.1 L5159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:62286411 C>G maps to NM_001620.1 L5159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:62297748 C>T maps to NM_001620.1 L1380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:62297748 C>T maps to NM_001620.1 L1380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:64536577 G>C maps to NM_201995.2 S268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:64536577 G>C maps to NM_201995.2 S268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:74056564 G>C maps to NM_173582.3 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:74056564 G>C maps to NM_173582.3 V389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:74799888 G>C maps to NM_001005285.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:74799888 G>C maps to NM_001005285.1 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:94179019 G>C maps to NM_005591.3 S608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:94179019 G>C maps to NM_005591.3 S608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:102195710 G>A maps to NM_182962.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:102195710 G>A maps to NM_182962.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:113281595 C>T maps to ENST00000355319 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr11:113281595 C>T maps to ENST00000355319 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:50027426 C>G maps to NM_001031698.1 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:50027426 C>G maps to NM_001031698.1 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:58018659 C>T maps to NM_133489.2 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:58018659 C>T maps to NM_133489.2 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:67699869 C>T maps to NM_018448.3 R808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:67699869 C>T maps to NM_018448.3 R808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:75444682 G>A maps to NM_139137.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:75444682 G>A maps to NM_139137.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:81613829 C>A maps to NM_024560.2 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:81613829 C>A maps to NM_024560.2 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:117603391 C>T maps to NM_033624.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:117603391 C>T maps to NM_033624.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:121670828 C>T maps to NM_002560.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:121670828 C>T maps to NM_002560.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:121670849 C>G maps to NM_002560.2 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr12:121670849 C>G maps to NM_002560.2 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr13:35751192 C>T maps to ENST00000400445 Q1539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr13:35751192 C>T maps to ENST00000400445 Q1539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr13:48563042 G>A maps to NM_003850.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr13:48563042 G>A maps to NM_003850.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr13:114781702 C>T maps to ENST00000389544 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr13:114781702 C>T maps to ENST00000389544 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr14:23745035 C>T maps to NM_020834.2 E467E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr14:23745035 C>T maps to NM_020834.2 E467E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr14:88935897 G>T maps to NM_007039.3 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr14:88935897 G>T maps to NM_007039.3 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr14:100789774 C>T maps to NM_207117.2 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr14:100789774 C>T maps to NM_207117.2 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr15:41602044 C>G maps to NM_007280.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr15:41602044 C>G maps to NM_007280.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr15:52069168 C>T maps to NM_014548.3 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr15:52069168 C>T maps to NM_014548.3 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr15:52905992 C>T maps to NM_019600.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr15:52905992 C>T maps to NM_019600.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr15:64791722 C>T maps to NM_015042.1 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr15:64791722 C>T maps to NM_015042.1 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr15:73616078 G>A maps to NM_005477.2 A785A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr15:73616078 G>A maps to NM_005477.2 A785A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr15:83221345 C>A maps to ENST00000261723 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr15:83221345 C>A maps to ENST00000261723 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr16:67573996 C>T maps to NM_001193523.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr16:67573996 C>T maps to NM_001193523.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:455170 G>A maps to NM_001128159.2 Q603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:455170 G>A maps to NM_001128159.2 Q603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:3119609 C>T maps to NM_014565.2 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:3119609 C>T maps to NM_014565.2 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:7753195 G>A maps to NM_001080424.1 V1166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:7753195 G>A maps to NM_001080424.1 V1166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:18220059 G>A maps to NM_144775.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:18220059 G>A maps to NM_144775.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:26114729 G>A maps to NM_000625.4 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:26114729 G>A maps to NM_000625.4 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:38978335 C>A maps to NM_000421.3 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:38978335 C>A maps to NM_000421.3 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:39975507 G>C maps to NM_021939.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:39975507 G>C maps to NM_021939.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:43159089 G>A maps to NM_021079.3 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:43159089 G>A maps to NM_021079.3 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:43364680 C>A maps to ENST00000344686 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:43364680 C>A maps to ENST00000344686 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:46926687 C>A maps to ENST00000448105 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:46926687 C>A maps to ENST00000448105 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:47388698 G>A maps to NM_014897.2 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:47388698 G>A maps to NM_014897.2 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:58288741 G>C maps to NM_032582.3 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:58288741 G>C maps to NM_032582.3 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:61512583 G>A maps to NM_001915.3 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:61512583 G>A maps to NM_001915.3 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:61611638 C>T maps to NM_030779.2 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:61611638 C>T maps to NM_030779.2 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:66972083 C>T maps to NM_080283.3 W1616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:66972083 C>T maps to NM_080283.3 W1616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:79632427 C>A maps to NM_001039842.1 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr17:79632427 C>A maps to NM_001039842.1 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr18:9256443 C>G maps to NM_015208.3 S1060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr18:9256443 C>G maps to NM_015208.3 S1060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr18:60642650 G>A maps to NM_194449.2 Q1259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr18:60642650 G>A maps to NM_194449.2 Q1259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr18:72183551 G>A maps to NM_018235.2 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr18:72183551 G>A maps to NM_018235.2 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:1109707 G>A maps to NM_014963.2 Q1033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:1109707 G>A maps to NM_014963.2 Q1033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:2110820 G>A maps to ENST00000355272 S1020S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:2110820 G>A maps to ENST00000355272 S1020S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:3028340 C>A maps to NM_003260.4 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:3028340 C>A maps to NM_003260.4 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:3494055 C>T maps to NM_001145165.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:3494055 C>T maps to NM_001145165.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:11036434 G>A maps to NM_024029.3 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:11036434 G>A maps to NM_024029.3 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:21992316 G>A maps to NM_003423.2 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:21992316 G>A maps to NM_003423.2 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:39989649 G>A maps to NM_016941.3 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:39989649 G>A maps to NM_016941.3 Q12Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:42753747 G>A maps to NM_006494.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:42753747 G>A maps to NM_006494.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:49477903 G>A maps to NM_002103.4 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:49477903 G>A maps to NM_002103.4 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:52091026 G>A maps to NM_007147.2 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr19:52091026 G>A maps to NM_007147.2 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:8871879 G>C maps to NM_020738.2 S1429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:8871879 G>C maps to NM_020738.2 S1429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:32605288 C>T maps to NM_016252.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:32605288 C>T maps to NM_016252.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:74757144 G>A maps to NM_013247.4 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:74757144 G>A maps to NM_013247.4 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:75100415 C>G maps to NM_000189.4 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:75100415 C>G maps to NM_000189.4 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:191859794 G>C maps to NM_007315.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:191859794 G>C maps to NM_007315.3 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:220111833 G>C did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:220111833 G>C did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:234888875 G>T maps to NM_024080.4 V800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:234888875 G>T maps to NM_024080.4 V800V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:242194962 C>G maps to NM_005336.3 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr2:242194962 C>G maps to NM_005336.3 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr20:30584821 C>G maps to NM_001011718.1 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr20:30584821 C>G maps to NM_001011718.1 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr20:31022344 C>T maps to ENST00000375687 G610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr20:31022344 C>T maps to ENST00000375687 G610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr20:43047075 C>T maps to ENST00000338692 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr20:43047075 C>T maps to ENST00000338692 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr20:50049029 G>A maps to NM_012340.3 Q766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr20:50049029 G>A maps to NM_012340.3 Q766*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr21:46226907 C>T maps to ENST00000411651 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr21:46226907 C>T maps to ENST00000411651 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr21:47546044 C>G maps to NM_001849.3 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr21:47546044 C>G maps to NM_001849.3 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr22:30660369 C>T maps to NM_020530.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr22:30660369 C>T maps to NM_020530.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:3887185 T>C maps to NM_020873.5 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:3887185 T>C maps to NM_020873.5 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:8940659 C>A maps to NM_020165.3 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:8940659 C>A maps to NM_020165.3 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:24003915 C>T maps to NM_005126.4 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:24003915 C>T maps to NM_005126.4 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:40223838 G>A maps to NM_015460.2 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:40223838 G>A maps to NM_015460.2 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:47448092 C>G maps to NM_015466.2 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:47448092 C>G maps to NM_015466.2 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:47484420 G>A maps to NM_012235.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:47484420 G>A maps to NM_012235.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:50334678 C>A maps to NM_012191.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:50334678 C>A maps to NM_012191.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:53834388 C>T maps to NM_001128840.1 F1679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:53834388 C>T maps to NM_001128840.1 F1679F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:108380810 C>T maps to NM_014648.3 Q763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:108380810 C>T maps to NM_014648.3 Q763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:127298672 G>A maps to NM_001136053.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:127298672 G>A maps to NM_001136053.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:164733861 G>A maps to NM_001041.3 Q1256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:164733861 G>A maps to NM_001041.3 Q1256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:164906953 G>C maps to NM_014926.2 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:164906953 G>C maps to NM_014926.2 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:184039823 C>T maps to NM_001194947.1 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:184039823 C>T maps to NM_001194947.1 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:195965714 C>T maps to NM_005017.2 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr3:195965714 C>T maps to NM_005017.2 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr4:25676181 C>T maps to NM_006424.2 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr4:25676181 C>T maps to NM_006424.2 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr4:74853900 G>A did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr4:74853900 G>A did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr4:123844434 G>A maps to NM_145207.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr4:123844434 G>A maps to NM_145207.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr4:126238051 G>T maps to NM_024582.4 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr4:126238051 G>T maps to NM_024582.4 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr4:187628328 G>A maps to ENST00000260147 R885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr4:187628328 G>A maps to ENST00000260147 R885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr5:33455162 C>T maps to ENST00000455217 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr5:33455162 C>T maps to ENST00000455217 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr5:102472490 C>T maps to ENST00000451606 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr5:102472490 C>T maps to ENST00000451606 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr5:107700444 G>C maps to NM_001163315.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr5:107700444 G>C maps to NM_001163315.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr5:132439955 C>G maps to NM_002154.3 S784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr5:132439955 C>G maps to NM_002154.3 S784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr5:147715229 C>T maps to NM_001040433.1 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr5:147715229 C>T maps to NM_001040433.1 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr5:153390821 G>A maps to ENST00000442256 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr5:153390821 G>A maps to ENST00000442256 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:26017459 C>T maps to NM_005325.3 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:26017459 C>T maps to NM_005325.3 K167K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:29912343 G>A maps to ENST00000376806 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:29912343 G>A maps to ENST00000376806 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:31525603 G>A maps to NM_005007.3 Q178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:31525603 G>A maps to NM_005007.3 Q178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:31548551 G>A maps to NM_002341.1 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:31548551 G>A maps to NM_002341.1 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:31974816 C>T maps to NM_000500.5 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:31974816 C>T maps to NM_000500.5 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:46660212 G>T maps to NM_001010870.2 E1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:46660212 G>T maps to NM_001010870.2 E1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:49704109 C>T maps to NM_001190986.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:49704109 C>T maps to NM_001190986.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:49754449 G>A maps to NM_138733.4 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:49754449 G>A maps to NM_138733.4 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:143486274 G>A maps to NM_016108.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:143486274 G>A maps to NM_016108.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:151939128 G>A maps to ENST00000367290 V672V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:151939128 G>A maps to ENST00000367290 V672V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:160164725 G>T maps to NM_004906.3 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr6:160164725 G>T maps to NM_004906.3 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:21678665 G>T maps to NM_003777.3 G1648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:21678665 G>T maps to NM_003777.3 G1648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:31614169 G>T maps to NM_194300.2 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:31614169 G>T maps to NM_194300.2 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:48147941 G>T maps to NM_003364.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:48147941 G>T maps to NM_003364.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:87179591 C>G maps to NM_000927.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:87179591 C>G maps to NM_000927.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:99489923 C>T maps to NM_033017.3 G455G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:99489923 C>T maps to NM_033017.3 G455G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:112124969 C>T maps to NM_182597.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:112124969 C>T maps to NM_182597.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:142605908 G>C maps to NM_019841.4 S654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:142605908 G>C maps to NM_019841.4 S654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:149482280 C>G maps to NM_198455.2 P986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr7:149482280 C>G maps to NM_198455.2 P986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr8:17731929 G>A maps to NM_201552.1 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr8:17731929 G>A maps to NM_201552.1 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr8:23538826 G>C maps to NM_006167.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr8:23538826 G>C maps to NM_006167.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr8:37687367 G>T did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr8:37687367 G>T did not map to a codon.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr8:67759504 G>C maps to NM_013257.3 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr8:67759504 G>C maps to NM_013257.3 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr8:67926686 G>C maps to ENST00000421742 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr8:67926686 G>C maps to ENST00000421742 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:117888 G>A maps to NM_207305.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:117888 G>A maps to NM_207305.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:21409279 G>A maps to NM_002170.3 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:21409279 G>A maps to NM_002170.3 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:37486583 C>T maps to ENST00000377792 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:37486583 C>T maps to ENST00000377792 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:70177785 C>G maps to NM_001126334.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:70177785 C>G maps to NM_001126334.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:77354740 G>A maps to NM_017662.4 L1795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:77354740 G>A maps to NM_017662.4 L1795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:101765754 G>C maps to NM_001855.3 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:101765754 G>C maps to NM_001855.3 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:114134892 G>A maps to NM_001080398.1 I1626I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:114134892 G>A maps to NM_001080398.1 I1626I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:119460353 C>T maps to NM_012210.3 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:119460353 C>T maps to NM_012210.3 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:129851243 G>A maps to NM_012098.2 R486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:129851243 G>A maps to NM_012098.2 R486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:130569915 C>T maps to NM_004957.4 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:130569915 C>T maps to NM_004957.4 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:131084582 C>G maps to NM_015679.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:131084582 C>G maps to NM_015679.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:139402741 C>T maps to NM_017617.3 W1089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:139402741 C>T maps to NM_017617.3 W1089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:139686221 C>T maps to NM_032928.3 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chr9:139686221 C>T maps to NM_032928.3 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chrX:55247871 T>C maps to NM_130467.3 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chrX:55247871 T>C maps to NM_130467.3 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chrX:100505952 C>T maps to NM_001939.2 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chrX:100505952 C>T maps to NM_001939.2 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chrX:100911313 G>A maps to NM_177949.2 Q421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chrX:100911313 G>A maps to NM_177949.2 Q421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chrX:103498856 G>A maps to NM_153448.3 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chrX:103498856 G>A maps to NM_153448.3 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chrX:136113290 G>C maps to NM_054021.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chrX:136113290 G>C maps to NM_054021.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chrX:153006072 G>A maps to NM_000033.3 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7427-01A-11D-2078-08 chrX:153006072 G>A maps to NM_000033.3 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr1:25245772 G>A maps to NM_001031680.2 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr1:25245772 G>A maps to NM_001031680.2 R182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr1:27088728 C>T maps to NM_006015.4 Q780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr1:27088728 C>T maps to NM_006015.4 Q780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr1:62321820 T>C maps to NM_176877.2 C744C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr1:62321820 T>C maps to NM_176877.2 C744C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr1:100550934 C>T maps to NM_194292.1 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr1:100550934 C>T maps to NM_194292.1 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr1:154962991 C>T maps to NM_025207.4 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr1:154962991 C>T maps to NM_025207.4 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr1:165721336 A>G did not map to a codon.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr1:165721336 A>G did not map to a codon.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr10:73569778 C>T maps to ENST00000398860 F2980F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr10:73569778 C>T maps to ENST00000398860 F2980F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr11:17548773 C>T maps to NM_153676.3 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr11:17548773 C>T maps to NM_153676.3 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr12:48142707 C>A maps to NM_001098531.2 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr12:48142707 C>A maps to NM_001098531.2 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr12:58008470 G>T did not map to a codon.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr12:58008470 G>T did not map to a codon.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr12:112667558 G>A maps to NM_001109662.2 A1982A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr12:112667558 G>A maps to NM_001109662.2 A1982A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr15:31197066 T>C maps to NM_014967.4 N67N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr15:31197066 T>C maps to NM_014967.4 N67N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr16:3726127 G>A maps to NM_016292.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr16:3726127 G>A maps to NM_016292.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr16:3779590 G>T maps to NM_004380.2 C1819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr16:3779590 G>T maps to NM_004380.2 C1819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr17:1375217 G>A maps to NM_001080779.1 Y668Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr17:1375217 G>A maps to NM_001080779.1 Y668Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr17:68172220 T>G maps to NM_000891.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr17:68172220 T>G maps to NM_000891.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr18:74536253 C>T did not map to a codon.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr18:74536253 C>T did not map to a codon.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr2:179600757 T>C maps to NM_133378.4 T3561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr2:179600757 T>C maps to NM_133378.4 T3561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr20:44516181 G>A maps to NM_080608.3 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr20:44516181 G>A maps to NM_080608.3 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr21:47412127 C>T maps to NM_001848.2 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr21:47412127 C>T maps to NM_001848.2 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr4:69962246 G>A maps to NM_001074.2 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr4:69962246 G>A maps to NM_001074.2 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr5:153826343 C>A maps to NM_024632.5 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7429-01A-11D-2129-08 chr5:153826343 C>A maps to NM_024632.5 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr1:17256381 G>T maps to NM_014675.3 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr1:17256381 G>T maps to NM_014675.3 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr1:86913312 A>G maps to NM_006536.5 E612E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr1:86913312 A>G maps to NM_006536.5 E612E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr1:151774778 C>T maps to NM_001004432.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr1:151774778 C>T maps to NM_001004432.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr1:248458472 C>T maps to NM_001004692.1 W136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr1:248458472 C>T maps to NM_001004692.1 W136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr10:108371725 C>T maps to NM_001013031.1 P992P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr10:108371725 C>T maps to NM_001013031.1 P992P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr11:68696741 C>T maps to NM_002180.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr11:68696741 C>T maps to NM_002180.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr12:21918865 G>A maps to NM_004982.2 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr12:21918865 G>A maps to NM_004982.2 R356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr12:108634151 C>T maps to ENST00000261400 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr12:108634151 C>T maps to ENST00000261400 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr12:109016913 C>A maps to ENST00000228463 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr12:109016913 C>A maps to ENST00000228463 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr15:23811474 C>T maps to NM_005664.3 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr15:23811474 C>T maps to NM_005664.3 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr16:61859021 A>T maps to NM_001796.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr16:61859021 A>T maps to NM_001796.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr16:68729735 C>T maps to NM_001793.4 L730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr16:68729735 C>T maps to NM_001793.4 L730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr16:76555133 T>C maps to NM_033401.3 F820F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr16:76555133 T>C maps to NM_033401.3 F820F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr16:88689625 G>A did not map to a codon.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr16:88689625 G>A did not map to a codon.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr17:10369588 C>A did not map to a codon.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr17:10369588 C>A did not map to a codon.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr17:68171809 G>A maps to NM_000891.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr17:68171809 G>A maps to NM_000891.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr17:74019474 C>T maps to NM_001988.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr17:74019474 C>T maps to NM_001988.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr19:12975623 C>T maps to NM_014975.2 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr19:12975623 C>T maps to NM_014975.2 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr19:53117346 G>A maps to NM_018300.3 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr19:53117346 G>A maps to NM_018300.3 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr2:1843126 C>A maps to ENST00000399161 G958G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr2:1843126 C>A maps to ENST00000399161 G958G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr2:27276858 C>A maps to NM_021831.5 Y161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr2:27276858 C>A maps to NM_021831.5 Y161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr2:128775457 G>A maps to NM_001145928.1 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr2:128775457 G>A maps to NM_001145928.1 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr2:155555886 G>T maps to NM_002239.2 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr2:155555886 G>T maps to NM_002239.2 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr2:196592976 C>T maps to NM_001127257.1 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr2:196592976 C>T maps to NM_001127257.1 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr20:61488811 C>T maps to NM_006602.2 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr20:61488811 C>T maps to NM_006602.2 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr21:41684251 T>C maps to NM_001389.3 R606R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr21:41684251 T>C maps to NM_001389.3 R606R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr22:26242141 C>G maps to ENST00000407587 G1150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr22:26242141 C>G maps to ENST00000407587 G1150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr3:108773581 G>T maps to NM_014429.3 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr3:108773581 G>T maps to NM_014429.3 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr3:169540248 C>T maps to NM_001080460.1 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr3:169540248 C>T maps to NM_001080460.1 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr3:180397179 G>C did not map to a codon.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr3:180397179 G>C did not map to a codon.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr4:153691670 C>T maps to NM_145720.2 W162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr4:153691670 C>T maps to NM_145720.2 W162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr4:164393620 C>G maps to NM_032136.4 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr4:164393620 C>G maps to NM_032136.4 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr5:32088329 G>T maps to NM_178140.2 S1592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr5:32088329 G>T maps to NM_178140.2 S1592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr5:56167805 A>T maps to NM_005921.1 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr5:56167805 A>T maps to NM_005921.1 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr6:7231220 G>A maps to NM_001003699.3 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr6:7231220 G>A maps to NM_001003699.3 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr6:148840965 G>A maps to NM_015278.3 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr6:148840965 G>A maps to NM_015278.3 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr9:119065051 C>A maps to NM_002581.3 C990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chr9:119065051 C>A maps to NM_002581.3 C990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chrX:21515964 G>A did not map to a codon.
Sequencing variant TCGA-CV-7430-01A-11D-2129-08 chrX:21515964 G>A did not map to a codon.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr1:120387064 T>A maps to NM_001047980.1 K32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr1:120387064 T>A maps to NM_001047980.1 K32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr1:240975266 C>A maps to ENST00000407727 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr1:240975266 C>A maps to ENST00000407727 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr10:16949519 G>T maps to NM_001081.3 S2564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr10:16949519 G>T maps to NM_001081.3 S2564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr11:6632500 G>A maps to NM_006284.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr11:6632500 G>A maps to NM_006284.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr12:7028877 T>A maps to NM_001975.2 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr12:7028877 T>A maps to NM_001975.2 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr13:60485886 A>T maps to NM_001042517.1 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr13:60485886 A>T maps to NM_001042517.1 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr13:92797192 C>T maps to NM_004466.4 C504C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr13:92797192 C>T maps to NM_004466.4 C504C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr14:20768885 C>A maps to NM_138376.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr14:20768885 C>A maps to NM_138376.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr14:23450598 G>A maps to NM_032876.4 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr14:23450598 G>A maps to NM_032876.4 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr14:72054660 C>T maps to NM_015556.1 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr14:72054660 C>T maps to NM_015556.1 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr16:67218810 G>A maps to NM_178516.3 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr16:67218810 G>A maps to NM_178516.3 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr16:68894424 G>T maps to NM_024562.1 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr16:68894424 G>T maps to NM_024562.1 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr17:7495897 T>C maps to NM_004860.3 Q583Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr17:7495897 T>C maps to NM_004860.3 Q583Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr17:10369619 G>A maps to NM_017533.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr17:10369619 G>A maps to NM_017533.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr18:7231432 G>A maps to NM_001105581.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr18:7231432 G>A maps to NM_001105581.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr19:1993105 C>T maps to NM_017797.3 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr19:1993105 C>T maps to NM_017797.3 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr19:12575298 T>C maps to ENST00000428311 K479K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr19:12575298 T>C maps to ENST00000428311 K479K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr19:41281723 C>T maps to NM_006533.2 H65H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr19:41281723 C>T maps to NM_006533.2 H65H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr19:53855799 T>C maps to NM_138374.1 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr19:53855799 T>C maps to NM_138374.1 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr2:79255000 G>A maps to NM_001008387.1 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr2:79255000 G>A maps to NM_001008387.1 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr2:114257666 C>A maps to NM_012184.4 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr2:114257666 C>A maps to NM_012184.4 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr2:228148996 A>G maps to NM_000091.4 K939K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr2:228148996 A>G maps to NM_000091.4 K939K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr2:239090739 G>T maps to NM_030768.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr2:239090739 G>T maps to NM_030768.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr20:16712385 T>C maps to NM_198220.2 N13N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr20:16712385 T>C maps to NM_198220.2 N13N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr20:23860166 G>A maps to NM_001900.4 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr20:23860166 G>A maps to NM_001900.4 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr20:60893706 C>A did not map to a codon.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr20:60893706 C>A did not map to a codon.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr21:31744359 C>A maps to NM_181621.3 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr21:31744359 C>A maps to NM_181621.3 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr22:26830195 C>T maps to NM_020437.4 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr22:26830195 C>T maps to NM_020437.4 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr3:13370374 C>T maps to NM_024923.2 V1394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr3:13370374 C>T maps to NM_024923.2 V1394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr3:123512631 C>T maps to NM_053025.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr3:123512631 C>T maps to NM_053025.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr4:96762053 G>A maps to NM_005390.4 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr4:96762053 G>A maps to NM_005390.4 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:11023089 G>T maps to NM_001332.2 G930G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:11023089 G>T maps to NM_001332.2 G930G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:31316321 A>G maps to NM_004932.2 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:31316321 A>G maps to NM_004932.2 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:63256466 G>A maps to NM_000524.2 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:63256466 G>A maps to NM_000524.2 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:95746663 G>A maps to NM_000439.4 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:95746663 G>A maps to NM_000439.4 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:140261864 C>T maps to NM_018904.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:140261864 C>T maps to NM_018904.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:140262128 C>T maps to NM_018904.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:140262128 C>T maps to NM_018904.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:149562460 G>A maps to NM_001804.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:149562460 G>A maps to NM_001804.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:153175080 C>G maps to NM_001114183.1 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:153175080 C>G maps to NM_001114183.1 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:168123339 G>A maps to NM_003062.2 D1013D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:168123339 G>A maps to NM_003062.2 D1013D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr6:49753699 C>A maps to NM_138733.4 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr6:49753699 C>A maps to NM_138733.4 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr6:53787548 C>T maps to NM_018214.4 N511N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr6:53787548 C>T maps to NM_018214.4 N511N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr6:90604420 G>A maps to NM_032602.1 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr6:90604420 G>A maps to NM_032602.1 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr6:111695450 T>C maps to NM_002912.3 A1369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr6:111695450 T>C maps to NM_002912.3 A1369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr6:144844226 G>T maps to NM_007124.2 E1937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr6:144844226 G>T maps to NM_007124.2 E1937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr6:152786397 T>A maps to NM_182961.2 K643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr6:152786397 T>A maps to NM_182961.2 K643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr7:6452470 G>A maps to NM_139179.3 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr7:6452470 G>A maps to NM_139179.3 R514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr7:149493813 G>A maps to NM_198455.2 L2271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr7:149493813 G>A maps to NM_198455.2 L2271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr8:2024314 G>A maps to NM_003970.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr8:2024314 G>A maps to NM_003970.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr8:91929768 T>A maps to NM_022351.4 L136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr8:91929768 T>A maps to NM_022351.4 L136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr8:98290054 C>A maps to NM_033512.2 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr8:98290054 C>A maps to NM_033512.2 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr9:75531988 C>T maps to NM_000689.3 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr9:75531988 C>T maps to NM_000689.3 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr9:128206806 A>G maps to NM_001006617.1 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr9:128206806 A>G maps to NM_001006617.1 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr9:135462839 C>T maps to NM_020064.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr9:135462839 C>T maps to NM_020064.3 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr9:136234282 C>T maps to NM_033161.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr9:136234282 C>T maps to NM_033161.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chrX:18606256 G>T maps to NM_001037343.1 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chrX:18606256 G>T maps to NM_001037343.1 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chrX:48419317 G>A maps to NM_002536.2 E674E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chrX:48419317 G>A maps to NM_002536.2 E674E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr19:54466452 G>A maps to NM_031895.5 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr19:54466452 G>A maps to NM_031895.5 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr20:2517942 G>A maps to NM_080751.2 K21K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr20:2517942 G>A maps to NM_080751.2 K21K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr1:16257102 A>G maps to NM_015001.2 S1456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr1:16257102 A>G maps to NM_015001.2 S1456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr1:155989898 T>A maps to ENST00000368312 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr1:155989898 T>A maps to ENST00000368312 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr1:160990821 G>C maps to NM_016946.4 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr1:160990821 G>C maps to NM_016946.4 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr1:196796098 C>A maps to NM_002113.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr1:196796098 C>A maps to NM_002113.2 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr1:220986690 G>C maps to NM_022746.3 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr1:220986690 G>C maps to NM_022746.3 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr10:112641195 C>T maps to NM_014456.4 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr10:112641195 C>T maps to NM_014456.4 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr11:14277227 C>A maps to NM_006108.2 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr11:14277227 C>A maps to NM_006108.2 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr11:48266855 C>T maps to NM_001004727.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr11:48266855 C>T maps to NM_001004727.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr11:65314017 C>A maps to NM_001130144.2 E750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr11:65314017 C>A maps to NM_001130144.2 E750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr11:124794744 A>G maps to NM_152722.4 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr11:124794744 A>G maps to NM_152722.4 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr12:7343014 C>T maps to NM_001131023.1 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr12:7343014 C>T maps to NM_001131023.1 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr12:10319440 T>A maps to NM_002543.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr12:10319440 T>A maps to NM_002543.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr12:69756668 G>C maps to NM_006530.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr12:69756668 G>C maps to NM_006530.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr12:110232202 G>A maps to NM_021625.4 N474N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr12:110232202 G>A maps to NM_021625.4 N474N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr14:88936011 G>T maps to NM_007039.3 T1022T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr14:88936011 G>T maps to NM_007039.3 T1022T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr15:56961079 G>A maps to NM_017661.2 Q496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr15:56961079 G>A maps to NM_017661.2 Q496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr15:91449138 G>T maps to NM_006122.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr15:91449138 G>T maps to NM_006122.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr16:29937219 C>T maps to NM_178863.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr16:29937219 C>T maps to NM_178863.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr17:18066631 C>T maps to ENST00000205890 C3229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr17:18066631 C>T maps to ENST00000205890 C3229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr17:27999101 C>T maps to NM_033389.2 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr17:27999101 C>T maps to NM_033389.2 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr17:74734466 C>T maps to NM_024311.2 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr17:74734466 C>T maps to NM_024311.2 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr19:30312986 G>T maps to NM_001238.1 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr19:30312986 G>T maps to NM_001238.1 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr2:8822624 C>T maps to NM_002166.4 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr2:8822624 C>T maps to NM_002166.4 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr2:200245203 T>A maps to NM_001172509.1 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr2:200245203 T>A maps to NM_001172509.1 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr20:10622311 G>A maps to NM_000214.2 L904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr20:10622311 G>A maps to NM_000214.2 L904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr22:18022153 G>A maps to ENST00000400579 W753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr22:18022153 G>A maps to ENST00000400579 W753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr22:24219247 G>A maps to NM_030807.3 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr22:24219247 G>A maps to NM_030807.3 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr22:29627076 G>T maps to NM_133455.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr22:29627076 G>T maps to NM_133455.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr22:38824020 C>T maps to NM_152868.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr22:38824020 C>T maps to NM_152868.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr3:48560991 C>G maps to NM_004567.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr3:48560991 C>G maps to NM_004567.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr3:156272785 G>C maps to ENST00000467789 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr3:156272785 G>C maps to ENST00000467789 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr4:46979497 G>C maps to NM_000809.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr4:46979497 G>C maps to NM_000809.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr4:78697452 T>C maps to ENST00000512485 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr4:78697452 T>C maps to ENST00000512485 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr5:63871703 C>T maps to NM_001029875.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr5:63871703 C>T maps to NM_001029875.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr6:7581447 C>T maps to NM_004415.2 V1675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr6:7581447 C>T maps to NM_004415.2 V1675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr6:32172088 T>A maps to NM_004557.3 G981G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr6:32172088 T>A maps to NM_004557.3 G981G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr6:47646750 C>T maps to NM_153839.6 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr6:47646750 C>T maps to NM_153839.6 Q50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr6:116938342 C>G maps to NM_001010892.2 S186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr6:116938342 C>G maps to NM_001010892.2 S186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr6:133769303 C>T maps to ENST00000452339 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr6:133769303 C>T maps to ENST00000452339 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr7:75171236 C>T did not map to a codon.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr7:75171236 C>T did not map to a codon.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr8:39782291 G>T did not map to a codon.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr8:39782291 G>T did not map to a codon.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr8:100493855 C>A maps to NM_017890.3 I1232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr8:100493855 C>A maps to NM_017890.3 I1232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr8:100796679 C>T maps to NM_017890.3 S2664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr8:100796679 C>T maps to NM_017890.3 S2664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr8:105503224 C>T maps to NM_013437.4 Q752Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7433-01A-11D-2129-08 chr8:105503224 C>T maps to NM_013437.4 Q752Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr1:103471420 C>T maps to NM_080629.2 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr1:103471420 C>T maps to NM_080629.2 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr1:111147062 C>T maps to NM_004974.2 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr1:111147062 C>T maps to NM_004974.2 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr1:152285837 C>T maps to NM_002016.1 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr1:152285837 C>T maps to NM_002016.1 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr1:196309632 G>A maps to NM_198503.2 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr1:196309632 G>A maps to NM_198503.2 R541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr10:126682530 C>A maps to NM_022802.2 V808V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr10:126682530 C>A maps to NM_022802.2 V808V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr11:3121472 C>T maps to NM_020896.3 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr11:3121472 C>T maps to NM_020896.3 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr11:63666241 A>G maps to NM_001039469.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr11:63666241 A>G maps to NM_001039469.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr11:68552320 G>A maps to NM_001876.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr11:68552320 G>A maps to NM_001876.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr11:105804579 G>T maps to NM_000829.3 E727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr11:105804579 G>T maps to NM_000829.3 E727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr11:130275887 G>A maps to NM_007037.4 N745N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr11:130275887 G>A maps to NM_007037.4 N745N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr12:49435982 G>A maps to NM_003482.3 Q2000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr12:49435982 G>A maps to NM_003482.3 Q2000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr12:51636286 C>T maps to ENST00000332845 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr12:51636286 C>T maps to ENST00000332845 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr12:52451147 C>A maps to ENST00000360284 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr12:52451147 C>A maps to ENST00000360284 G512G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr12:72176379 T>G maps to NM_014999.2 Y159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr12:72176379 T>G maps to NM_014999.2 Y159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr12:81545668 C>A maps to NM_024560.2 S323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr12:81545668 C>A maps to NM_024560.2 S323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr13:67802485 A>T maps to NM_203487.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr13:67802485 A>T maps to NM_203487.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr16:28497942 G>A maps to NM_000086.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr16:28497942 G>A maps to NM_000086.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr17:40282495 G>A maps to NM_201434.1 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr17:40282495 G>A maps to NM_201434.1 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr18:25593760 G>C maps to NM_001792.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr18:25593760 G>C maps to NM_001792.3 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr19:14805945 G>A did not map to a codon.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr19:14805945 G>A did not map to a codon.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr19:17941380 G>A maps to NM_000215.3 D1009D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr19:17941380 G>A maps to NM_000215.3 D1009D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr19:50302995 G>A maps to NM_014203.2 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr19:50302995 G>A maps to NM_014203.2 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr19:51914598 T>C maps to NM_033130.4 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr19:51914598 T>C maps to NM_033130.4 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr19:55239224 T>C maps to NM_153443.3 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr19:55239224 T>C maps to NM_153443.3 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr2:56420051 G>A maps to NM_001080433.1 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr2:56420051 G>A maps to NM_001080433.1 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr20:468127 G>A maps to NM_177559.2 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr20:468127 G>A maps to NM_177559.2 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr22:37322076 G>A maps to ENST00000262825 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr22:37322076 G>A maps to ENST00000262825 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr22:37695299 C>T maps to NM_013385.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr22:37695299 C>T maps to NM_013385.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr3:48451944 C>A maps to NM_001130082.1 G1813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr3:48451944 C>A maps to NM_001130082.1 G1813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr3:134884900 C>T maps to NM_004441.4 I559I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr3:134884900 C>T maps to NM_004441.4 I559I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr3:191098614 A>C did not map to a codon.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr3:191098614 A>C did not map to a codon.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr4:185940786 C>T maps to NM_001029887.1 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr4:185940786 C>T maps to NM_001029887.1 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr5:156346536 T>A maps to NM_138379.2 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr5:156346536 T>A maps to NM_138379.2 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr9:5233852 A>G maps to NM_002195.1 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr9:5233852 A>G maps to NM_002195.1 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr9:99522149 G>C maps to NM_014930.1 S321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr9:99522149 G>C maps to NM_014930.1 S321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr9:130507361 G>A maps to NM_170600.2 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr9:130507361 G>A maps to NM_170600.2 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr9:140811747 C>T maps to ENST00000277549 C277C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chr9:140811747 C>T maps to ENST00000277549 C277C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chrX:76776334 T>C maps to NM_000489.3 Q2377Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7434-01A-11D-2129-08 chrX:76776334 T>C maps to NM_000489.3 Q2377Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr1:38227470 G>A maps to NM_001099439.1 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr1:38227470 G>A maps to NM_001099439.1 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr1:60314746 T>G maps to NM_015888.4 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr1:60314746 T>G maps to NM_015888.4 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr1:144879068 G>A maps to NM_014644.4 L1461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr1:144879068 G>A maps to NM_014644.4 L1461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr1:145281459 A>G maps to ENST00000454606 K142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr1:145281459 A>G maps to ENST00000454606 K142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr10:64148196 G>A maps to NM_199451.2 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr10:64148196 G>A maps to NM_199451.2 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr10:99437757 C>T maps to NM_021732.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr10:99437757 C>T maps to NM_021732.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr14:62567239 C>T maps to NM_031914.2 Q585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr14:62567239 C>T maps to NM_031914.2 Q585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr16:321022 C>A maps to NM_183337.1 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr16:321022 C>A maps to NM_183337.1 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr17:7734766 G>C maps to NM_020877.2 G4173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr17:7734766 G>C maps to NM_020877.2 G4173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr2:202899736 C>T maps to NM_003507.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr2:202899736 C>T maps to NM_003507.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr20:45875010 G>A maps to ENST00000471951 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr20:45875010 G>A maps to ENST00000471951 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr22:33780225 G>A maps to NM_133642.3 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr22:33780225 G>A maps to NM_133642.3 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr3:126224561 G>A maps to NM_001165974.1 C265C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr3:126224561 G>A maps to NM_001165974.1 C265C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr3:194081301 G>A maps to NM_001135057.2 H163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr3:194081301 G>A maps to NM_001135057.2 H163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr5:41065469 G>A maps to ENST00000296803 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr5:41065469 G>A maps to ENST00000296803 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr5:131911504 C>T maps to NM_005732.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr5:131911504 C>T maps to NM_005732.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr5:167812358 C>T maps to NM_001161661.1 Q125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr5:167812358 C>T maps to NM_001161661.1 Q125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr8:30890026 C>T maps to NM_013357.2 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr8:30890026 C>T maps to NM_013357.2 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr8:117671058 G>A maps to ENST00000411422 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr8:117671058 G>A maps to ENST00000411422 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr9:88293286 A>T maps to ENST00000395847 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr9:88293286 A>T maps to ENST00000395847 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr9:131221863 G>A maps to NM_153435.1 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr9:131221863 G>A maps to NM_153435.1 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chrX:14883284 A>G maps to NM_152633.2 N116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chrX:14883284 A>G maps to NM_152633.2 N116N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr3:13611902 G>T maps to NM_001165035.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7435-01A-11D-2129-08 chr3:13611902 G>T maps to NM_001165035.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr1:33235550 C>T maps to NM_020888.2 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr1:33235550 C>T maps to NM_020888.2 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr1:92495662 C>G maps to NM_173567.4 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr1:92495662 C>G maps to NM_173567.4 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr1:120467944 C>T maps to NM_024408.2 G1498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr1:120467944 C>T maps to NM_024408.2 G1498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr1:150128283 G>T maps to ENST00000443480 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr1:150128283 G>T maps to ENST00000443480 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr1:155292475 C>T maps to NM_001105203.1 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr1:155292475 C>T maps to NM_001105203.1 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr1:167400950 G>A maps to NM_198053.2 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr1:167400950 G>A maps to NM_198053.2 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr1:206224959 C>T maps to NM_000707.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr1:206224959 C>T maps to NM_000707.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr10:931621 G>A maps to NM_015155.1 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr10:931621 G>A maps to NM_015155.1 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr10:45799804 A>G maps to NM_001004297.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr10:45799804 A>G maps to NM_001004297.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr10:63170316 G>A maps to NM_178505.6 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr10:63170316 G>A maps to NM_178505.6 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr12:7169970 G>A maps to NM_001734.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr12:7169970 G>A maps to NM_001734.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr12:7302137 G>T maps to NM_014718.3 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr12:7302137 G>T maps to NM_014718.3 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr12:49435963 C>T maps to NM_003482.3 W2006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr12:49435963 C>T maps to NM_003482.3 W2006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr12:56815167 C>T maps to NM_003920.3 K945K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr12:56815167 C>T maps to NM_003920.3 K945K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr12:57454715 C>T maps to NM_001130963.1 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr12:57454715 C>T maps to NM_001130963.1 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr13:92380811 A>T maps to NM_004466.4 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr13:92380811 A>T maps to NM_004466.4 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr14:58471867 T>G maps to ENST00000438670 V736V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr14:58471867 T>G maps to ENST00000438670 V736V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr17:71223342 A>G maps to NM_001098832.1 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr17:71223342 A>G maps to NM_001098832.1 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr18:77659521 C>T maps to NM_012283.1 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr18:77659521 C>T maps to NM_012283.1 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr19:15072830 C>A maps to NM_005071.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr19:15072830 C>A maps to NM_005071.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr2:43927242 C>T maps to NM_172069.3 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr2:43927242 C>T maps to NM_172069.3 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr2:95815452 G>C maps to NM_032788.1 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr2:95815452 G>C maps to NM_032788.1 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr2:179463493 C>T maps to NM_133378.4 A16413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr2:179463493 C>T maps to NM_133378.4 A16413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr20:50234076 G>A maps to NM_006045.1 D789D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr20:50234076 G>A maps to NM_006045.1 D789D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr21:15538693 G>C maps to NM_198996.2 S262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr21:15538693 G>C maps to NM_198996.2 S262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr22:21349205 G>A maps to NM_006767.3 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr22:21349205 G>A maps to NM_006767.3 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr22:42383246 C>T maps to NM_145733.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr22:42383246 C>T maps to NM_145733.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr3:113672829 C>T maps to NM_173570.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr3:113672829 C>T maps to NM_173570.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr3:157820513 G>A maps to NM_003030.4 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr3:157820513 G>A maps to NM_003030.4 R194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr3:159605681 C>T maps to NM_001197113.1 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr3:159605681 C>T maps to NM_001197113.1 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr3:169540506 G>A maps to NM_001080460.1 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr3:169540506 G>A maps to NM_001080460.1 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr4:123377562 T>C maps to NM_000586.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr4:123377562 T>C maps to NM_000586.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr4:187205255 C>T maps to NM_000128.3 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr4:187205255 C>T maps to NM_000128.3 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr5:1416214 G>T maps to NM_001044.4 Y343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr5:1416214 G>T maps to NM_001044.4 Y343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr5:10239376 C>T maps to NM_199133.2 W36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr5:10239376 C>T maps to NM_199133.2 W36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr5:13830754 G>A maps to NM_001369.2 F2004F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr5:13830754 G>A maps to NM_001369.2 F2004F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr5:140431882 G>T maps to NM_013340.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr5:140431882 G>T maps to NM_013340.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr5:140554401 G>T maps to NM_018940.2 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr5:140554401 G>T maps to NM_018940.2 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr5:156770491 G>T maps to NM_001001343.3 S18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr5:156770491 G>T maps to NM_001001343.3 S18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr6:6266931 G>T maps to NM_000129.3 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr6:6266931 G>T maps to NM_000129.3 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr7:8790657 G>A maps to NM_152745.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr7:8790657 G>A maps to NM_152745.2 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr7:56007357 C>T maps to NM_182633.1 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr7:56007357 C>T maps to NM_182633.1 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr7:56120138 C>T maps to NM_001762.3 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr7:56120138 C>T maps to NM_001762.3 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr7:73477972 C>T maps to ENST00000358929 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr7:73477972 C>T maps to ENST00000358929 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr7:81620502 G>C maps to NM_000722.2 Y598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr7:81620502 G>C maps to NM_000722.2 Y598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr7:127014178 G>C maps to NM_176814.3 S404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr7:127014178 G>C maps to NM_176814.3 S404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr7:150174741 G>T maps to NM_175571.2 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr7:150174741 G>T maps to NM_175571.2 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr8:22864370 C>T maps to NM_001160036.1 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr8:22864370 C>T maps to NM_001160036.1 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr8:38264943 C>A maps to ENST00000379957 S459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr8:38264943 C>A maps to ENST00000379957 S459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr8:52321225 G>A maps to NM_144651.4 S986S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr8:52321225 G>A maps to NM_144651.4 S986S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr9:71532546 G>A maps to NM_003558.2 E285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr9:71532546 G>A maps to NM_003558.2 E285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr9:73151426 G>A maps to ENST00000419692 S1488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr9:73151426 G>A maps to ENST00000419692 S1488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chrX:15270436 G>A maps to NM_001031739.2 H124H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chrX:15270436 G>A maps to NM_001031739.2 H124H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr5:1033580 G>A maps to NM_033120.2 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr5:1033580 G>A maps to NM_033120.2 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr9:38396908 A>G maps to NM_000692.3 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7437-01A-21D-2129-08 chr9:38396908 A>G maps to NM_000692.3 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr1:19478947 C>T maps to ENST00000375267 V2285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr1:19478947 C>T maps to ENST00000375267 V2285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr1:28208650 C>G maps to NM_001105556.1 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr1:28208650 C>G maps to NM_001105556.1 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr1:110709556 G>A maps to NM_001010898.2 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr1:110709556 G>A maps to NM_001010898.2 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr1:157557114 C>G maps to NM_031282.2 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr1:157557114 C>G maps to NM_031282.2 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr10:72511851 G>T maps to NM_139155.2 G869G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr10:72511851 G>T maps to NM_139155.2 G869G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr10:97956811 G>C maps to NM_013314.3 S368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr10:97956811 G>C maps to NM_013314.3 S368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr11:66811317 G>A maps to NM_001177880.1 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr11:66811317 G>A maps to NM_001177880.1 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr11:86662819 A>G maps to NM_012193.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr11:86662819 A>G maps to NM_012193.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr12:57571374 G>T did not map to a codon.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr12:57571374 G>T did not map to a codon.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr12:59272719 C>A maps to NM_153377.3 E657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr12:59272719 C>A maps to NM_153377.3 E657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr14:47530569 T>C maps to NM_001113498.2 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr14:47530569 T>C maps to NM_001113498.2 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr15:45428811 C>T maps to NM_175940.1 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr15:45428811 C>T maps to NM_175940.1 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr17:48245849 C>T maps to NM_000023.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr17:48245849 C>T maps to NM_000023.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr19:7747351 G>A maps to NM_001042461.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr19:7747351 G>A maps to NM_001042461.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr19:11470245 C>G maps to NM_022737.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr19:11470245 C>G maps to NM_022737.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr19:15918403 G>A maps to NM_013940.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr19:15918403 G>A maps to NM_013940.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr19:35791164 C>T maps to NM_002361.3 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr19:35791164 C>T maps to NM_002361.3 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr19:40887042 G>C maps to NM_144685.3 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr19:40887042 G>C maps to NM_144685.3 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr19:41932173 C>T maps to NM_198540.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr19:41932173 C>T maps to NM_198540.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr2:99013474 G>A maps to NM_001298.2 E614E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr2:99013474 G>A maps to NM_001298.2 E614E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr2:99013492 C>T maps to NM_001298.2 G620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr2:99013492 C>T maps to NM_001298.2 G620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr2:177036311 C>T maps to NM_006898.4 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr2:177036311 C>T maps to NM_006898.4 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr2:220033734 A>T did not map to a codon.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr2:220033734 A>T did not map to a codon.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr20:17434529 C>T maps to NM_002594.2 Y343Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr20:17434529 C>T maps to NM_002594.2 Y343Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr20:23065974 G>A maps to NM_012072.3 C285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr20:23065974 G>A maps to NM_012072.3 C285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr20:35929758 C>T maps to NM_022077.3 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr20:35929758 C>T maps to NM_022077.3 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr20:39978494 C>T maps to NM_022896.1 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr20:39978494 C>T maps to NM_022896.1 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr3:9757197 C>T maps to ENST00000383832 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr3:9757197 C>T maps to ENST00000383832 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr3:100963245 C>T maps to NM_016247.2 E643E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr3:100963245 C>T maps to NM_016247.2 E643E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr3:129180116 C>T maps to NM_052985.2 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr3:129180116 C>T maps to NM_052985.2 Q158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr5:140180883 C>A maps to NM_018906.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr5:140180883 C>A maps to NM_018906.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr6:33288180 G>A maps to NM_001350.4 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr6:33288180 G>A maps to NM_001350.4 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr6:107854756 C>T maps to NM_018013.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr6:107854756 C>T maps to NM_018013.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr8:80954858 A>T maps to NM_001025252.1 L184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr8:80954858 A>T maps to NM_001025252.1 L184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr9:119093590 C>T maps to NM_002581.3 I1072I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chr9:119093590 C>T maps to NM_002581.3 I1072I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chrX:107417816 T>C maps to NM_033641.2 P997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chrX:107417816 T>C maps to NM_033641.2 P997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chrX:134483214 G>T maps to NM_152695.5 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chrX:134483214 G>T maps to NM_152695.5 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chrX:152710828 G>A maps to ENST00000402951 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chrX:152710828 G>A maps to ENST00000402951 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chrX:153740199 T>A maps to ENST00000369641 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7438-01A-21D-2129-08 chrX:153740199 T>A maps to ENST00000369641 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr1:16477389 C>G did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr1:16477389 C>G did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr1:27100150 C>A maps to NM_006015.4 S1316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr1:27100150 C>A maps to NM_006015.4 S1316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr1:41101586 C>A did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr1:41101586 C>A did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr1:103405900 A>T maps to NM_080629.2 P1134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr1:103405900 A>T maps to NM_080629.2 P1134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr1:215752340 A>G did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr1:215752340 A>G did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr10:5789009 C>G maps to NM_017782.4 S1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr10:5789009 C>G maps to NM_017782.4 S1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr10:5790609 G>A maps to NM_017782.4 K1742K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr10:5790609 G>A maps to NM_017782.4 K1742K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr10:5953001 G>T maps to NM_032807.3 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr10:5953001 G>T maps to NM_032807.3 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr10:37419230 T>G maps to ENST00000374660 Y89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr10:37419230 T>G maps to ENST00000374660 Y89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr10:46322016 C>T maps to ENST00000355953 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr10:46322016 C>T maps to ENST00000355953 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr10:50820231 C>T maps to NM_003055.2 R482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr10:50820231 C>T maps to NM_003055.2 R482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr10:101591888 G>A did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr10:101591888 G>A did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr11:5799294 G>A maps to NM_001001922.2 H190H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr11:5799294 G>A maps to NM_001001922.2 H190H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr11:111796826 G>T maps to NM_080659.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr11:111796826 G>T maps to NM_080659.2 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr11:113105875 G>A maps to ENST00000316851 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr11:113105875 G>A maps to ENST00000316851 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr11:120984287 C>T maps to NM_005422.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr11:120984287 C>T maps to NM_005422.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr12:26818844 G>A maps to NM_002223.2 Q517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr12:26818844 G>A maps to NM_002223.2 Q517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr12:55615023 T>C maps to NM_001005280.1 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr12:55615023 T>C maps to NM_001005280.1 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr12:81331468 C>A maps to NM_004664.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr12:81331468 C>A maps to NM_004664.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr14:59112624 C>A maps to NM_016651.5 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr14:59112624 C>A maps to NM_016651.5 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr14:94088413 C>G maps to ENST00000393153 S1634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr14:94088413 C>G maps to ENST00000393153 S1634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr15:54003098 G>T maps to NM_182758.2 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr15:54003098 G>T maps to NM_182758.2 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr15:65959831 T>C maps to ENST00000443035 L1732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr15:65959831 T>C maps to ENST00000443035 L1732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr17:10362565 A>T did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr17:10362565 A>T did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr17:64062992 A>G maps to NM_145036.3 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr17:64062992 A>G maps to NM_145036.3 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr17:64881203 C>T maps to NM_145811.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr17:64881203 C>T maps to NM_145811.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr18:44559421 C>T maps to NM_016427.2 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr18:44559421 C>T maps to NM_016427.2 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr19:15760803 A>T maps to NM_000896.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr19:15760803 A>T maps to NM_000896.2 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr19:53612055 G>A maps to NM_001164309.1 C414C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr19:53612055 G>A maps to NM_001164309.1 C414C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr19:54313979 G>T maps to ENST00000391773 C311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr19:54313979 G>T maps to ENST00000391773 C311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr19:54761047 G>A maps to NM_001081442.1 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr19:54761047 G>A maps to NM_001081442.1 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr2:97370098 G>A maps to NM_001113382.1 P2019P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr2:97370098 G>A maps to NM_001113382.1 P2019P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr2:141128762 A>G maps to NM_018557.2 A3620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr2:141128762 A>G maps to NM_018557.2 A3620A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr2:149226942 A>T maps to ENST00000404807 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr2:149226942 A>T maps to ENST00000404807 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr2:215880314 T>A maps to NM_173076.2 K619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr2:215880314 T>A maps to NM_173076.2 K619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr20:489117 G>T maps to NM_177559.2 Y26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr20:489117 G>T maps to NM_177559.2 Y26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr22:40800431 C>T maps to NM_015705.4 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr22:40800431 C>T maps to NM_015705.4 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr3:42727526 C>T maps to NM_152393.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr3:42727526 C>T maps to NM_152393.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr3:100963143 T>C maps to NM_016247.2 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr3:100963143 T>C maps to NM_016247.2 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr3:135969355 C>T maps to NM_001178014.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr3:135969355 C>T maps to NM_001178014.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr4:151504952 C>A maps to NM_006439.4 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr4:151504952 C>A maps to NM_006439.4 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr4:158060001 G>T maps to NM_001166060.1 G218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr4:158060001 G>T maps to NM_001166060.1 G218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr4:166232679 T>C maps to NM_001161521.1 N438N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr4:166232679 T>C maps to NM_001161521.1 N438N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr5:9136621 C>A maps to NM_003966.2 A531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr5:9136621 C>A maps to NM_003966.2 A531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr5:63256580 C>T maps to NM_000524.2 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr5:63256580 C>T maps to NM_000524.2 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr5:140223206 G>C maps to NM_018911.2 T767T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr5:140223206 G>C maps to NM_018911.2 T767T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr5:168135106 T>G did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr5:168135106 T>G did not map to a codon.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr5:176005488 G>A maps to NM_001171976.1 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr5:176005488 G>A maps to NM_001171976.1 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr5:176637775 C>A maps to NM_022455.4 C792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr5:176637775 C>A maps to NM_022455.4 C792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr5:176721511 C>A maps to NM_022455.4 P2381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr5:176721511 C>A maps to NM_022455.4 P2381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr6:70778325 G>T maps to NM_001858.4 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr6:70778325 G>T maps to NM_001858.4 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr6:119341264 C>A maps to NM_024581.4 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr6:119341264 C>A maps to NM_024581.4 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr6:129714274 G>T maps to NM_000426.3 E1774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr6:129714274 G>T maps to NM_000426.3 E1774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr6:152665275 G>T maps to NM_182961.2 V4055V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr6:152665275 G>T maps to NM_182961.2 V4055V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr7:4188975 C>T maps to NM_152744.3 G1502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr7:4188975 C>T maps to NM_152744.3 G1502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr7:82582944 T>A maps to NM_033026.5 K2442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr7:82582944 T>A maps to NM_033026.5 K2442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr7:86479717 C>T maps to NM_000840.2 S808S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr7:86479717 C>T maps to NM_000840.2 S808S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr7:111379255 G>A maps to ENST00000428084 N1722N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr7:111379255 G>A maps to ENST00000428084 N1722N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr8:41572571 G>A maps to ENST00000415018 H541H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr8:41572571 G>A maps to ENST00000415018 H541H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr9:107547892 T>C maps to NM_005502.3 V2143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr9:107547892 T>C maps to NM_005502.3 V2143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chrX:12734431 T>A maps to ENST00000429478 C608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chrX:12734431 T>A maps to ENST00000429478 C608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chrX:111097061 T>A maps to NM_012471.2 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chrX:111097061 T>A maps to NM_012471.2 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chrX:142967321 T>A maps to NM_001012989.1 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chrX:142967321 T>A maps to NM_001012989.1 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr19:50766676 G>A maps to NM_001145809.1 K898K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr19:50766676 G>A maps to NM_001145809.1 K898K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr7:5342476 C>T maps to NM_153247.2 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7440-01A-11D-2129-08 chr7:5342476 C>T maps to NM_153247.2 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:866466 C>T maps to ENST00000443100 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:866466 C>T maps to ENST00000443100 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:62907260 T>C maps to NM_003368.4 Y91Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:62907260 T>C maps to NM_003368.4 Y91Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:117484583 C>T maps to NM_020440.2 N99N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:117484583 C>T maps to NM_020440.2 N99N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:144619880 A>C did not map to a codon.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:144619880 A>C did not map to a codon.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:147096738 C>T maps to NM_004326.2 N1420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:147096738 C>T maps to NM_004326.2 N1420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:173839374 T>C maps to NM_001122770.1 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:173839374 T>C maps to NM_001122770.1 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:220206925 G>C maps to NM_004446.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:220206925 G>C maps to NM_004446.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:223179193 A>G maps to NM_032890.2 R1485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr1:223179193 A>G maps to NM_032890.2 R1485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr11:57995516 G>A maps to NM_001004471.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr11:57995516 G>A maps to NM_001004471.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr11:103780423 A>T maps to NM_025208.4 *371K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr11:103780423 A>T maps to NM_025208.4 *371K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr11:125479464 C>T maps to NM_152713.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr11:125479464 C>T maps to NM_152713.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr12:57457025 G>A maps to NM_001130963.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr12:57457025 G>A maps to NM_001130963.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr12:66932902 C>A maps to ENST00000359742 G125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr12:66932902 C>A maps to ENST00000359742 G125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr15:40295428 C>T maps to NM_001013703.2 R1091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr15:40295428 C>T maps to NM_001013703.2 R1091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr17:1028580 G>A maps to NM_021962.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr17:1028580 G>A maps to NM_021962.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr17:19583337 T>G maps to NM_152908.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr17:19583337 T>G maps to NM_152908.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr17:47656377 C>T maps to ENST00000513748 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr17:47656377 C>T maps to ENST00000513748 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr19:9046407 C>T maps to NM_024690.2 E11741E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr19:9046407 C>T maps to NM_024690.2 E11741E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr19:44636170 C>T maps to NM_013362.2 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr19:44636170 C>T maps to NM_013362.2 A468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr19:44777754 T>C maps to NM_181756.1 Y314Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr19:44777754 T>C maps to NM_181756.1 Y314Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr2:3691422 G>T maps to ENST00000418971 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr2:3691422 G>T maps to ENST00000418971 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr2:74802647 T>A maps to NM_138804.3 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr2:74802647 T>A maps to NM_138804.3 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr2:80529786 G>T maps to NM_178839.4 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr2:80529786 G>T maps to NM_178839.4 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr2:193049122 C>T maps to NM_016192.2 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr2:193049122 C>T maps to NM_016192.2 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr21:31692053 A>G maps to NM_203405.1 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr21:31692053 A>G maps to NM_203405.1 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr22:31330914 G>C maps to ENST00000397641 V682V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr22:31330914 G>C maps to ENST00000397641 V682V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr22:51117038 C>T maps to NM_001080420.1 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr22:51117038 C>T maps to NM_001080420.1 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr3:169824652 G>T maps to NM_024947.3 S812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr3:169824652 G>T maps to NM_024947.3 S812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr3:186395210 G>T maps to NM_000412.2 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr3:186395210 G>T maps to NM_000412.2 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr5:71756462 C>G maps to NM_152625.1 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr5:71756462 C>G maps to NM_152625.1 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr5:140237237 C>T maps to NM_018901.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr5:140237237 C>T maps to NM_018901.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr5:140502788 A>T maps to NM_018938.2 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr5:140502788 A>T maps to NM_018938.2 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr6:31785353 C>T maps to NM_005345.5 I607I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr6:31785353 C>T maps to NM_005345.5 I607I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr7:98645384 G>A maps to NM_020429.2 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr7:98645384 G>A maps to NM_020429.2 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr9:34655638 G>A maps to NM_001142784.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7082-01A-11D-2012-08 chr9:34655638 G>A maps to NM_001142784.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr1:32673133 G>A maps to NM_001160042.1 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr1:32673133 G>A maps to NM_001160042.1 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr1:54060497 G>A maps to NM_147193.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr1:54060497 G>A maps to NM_147193.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr1:117644142 C>T maps to NM_003594.3 I1162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr1:117644142 C>T maps to NM_003594.3 I1162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr1:150956842 C>T maps to NM_003568.2 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr1:150956842 C>T maps to NM_003568.2 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr1:156779021 G>A maps to NM_001161441.1 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr1:156779021 G>A maps to NM_001161441.1 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr10:18827253 C>G maps to NM_201596.2 S483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr10:18827253 C>G maps to NM_201596.2 S483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr10:70156541 G>A maps to NM_017987.4 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr10:70156541 G>A maps to NM_017987.4 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr11:4936269 G>A maps to NM_001005238.1 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr11:4936269 G>A maps to NM_001005238.1 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr11:14899668 C>A maps to NM_024514.4 *502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr11:14899668 C>A maps to NM_024514.4 *502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr12:20876120 G>A maps to NM_017435.4 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr12:20876120 G>A maps to NM_017435.4 V373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr12:72667121 G>A maps to NM_013381.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr12:72667121 G>A maps to NM_013381.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr12:103352546 C>T maps to NM_004316.3 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr12:103352546 C>T maps to NM_004316.3 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr12:120572482 G>A maps to NM_006836.1 F2352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr12:120572482 G>A maps to NM_006836.1 F2352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr12:121164931 G>A maps to NM_000017.2 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr12:121164931 G>A maps to NM_000017.2 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr13:46656635 G>A maps to NM_001872.3 N108N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr13:46656635 G>A maps to NM_001872.3 N108N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr14:20248858 C>T maps to NM_001005500.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr14:20248858 C>T maps to NM_001005500.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr14:64716326 G>A maps to NM_001437.2 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr14:64716326 G>A maps to NM_001437.2 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr16:1891861 G>C maps to NM_001163560.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr16:1891861 G>C maps to NM_001163560.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr16:2495572 G>A maps to NM_001761.2 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr16:2495572 G>A maps to NM_001761.2 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr16:24955122 G>A maps to NM_001006634.1 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr16:24955122 G>A maps to NM_001006634.1 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr16:56839413 A>T did not map to a codon.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr16:56839413 A>T did not map to a codon.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr16:66759797 C>T maps to NM_006141.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr16:66759797 C>T maps to NM_006141.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr17:18881188 G>C maps to NM_001039999.2 S597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr17:18881188 G>C maps to NM_001039999.2 S597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr18:743307 G>A maps to NM_005433.3 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr18:743307 G>A maps to NM_005433.3 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr19:36357105 G>A maps to NM_199180.2 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr19:36357105 G>A maps to NM_199180.2 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr19:45490455 G>A maps to NM_001294.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr19:45490455 G>A maps to NM_001294.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr19:52658815 G>C maps to NM_001102657.1 S707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr19:52658815 G>C maps to NM_001102657.1 S707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr19:59063498 C>T maps to NM_014453.2 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr19:59063498 C>T maps to NM_014453.2 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr2:160229586 C>T maps to NM_013450.2 G1394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr2:160229586 C>T maps to NM_013450.2 G1394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr2:202151269 C>T maps to NM_001080125.1 Q524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr2:202151269 C>T maps to NM_001080125.1 Q524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr2:217279567 C>T maps to NM_014140.3 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr2:217279567 C>T maps to NM_014140.3 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr2:238283538 G>A maps to NM_004369.3 V1065V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr2:238283538 G>A maps to NM_004369.3 V1065V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr22:35658314 G>C did not map to a codon.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr22:35658314 G>C did not map to a codon.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr3:123452807 G>A maps to NM_053025.3 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr3:123452807 G>A maps to NM_053025.3 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr3:160149429 G>A did not map to a codon.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr3:160149429 G>A did not map to a codon.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr3:180321059 G>A maps to NM_133462.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr3:180321059 G>A maps to NM_133462.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr4:76708300 G>A maps to NM_003715.2 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr4:76708300 G>A maps to NM_003715.2 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr5:33963898 G>C maps to NM_016180.3 S262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr5:33963898 G>C maps to NM_016180.3 S262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr5:131411511 C>T maps to NM_000758.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr5:131411511 C>T maps to NM_000758.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr6:26043603 C>T maps to NM_021062.2 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr6:26043603 C>T maps to NM_021062.2 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr6:30571942 C>T maps to NM_002714.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr6:30571942 C>T maps to NM_002714.2 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr6:39843214 G>A maps to ENST00000398904 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr6:39843214 G>A maps to ENST00000398904 E424E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr7:100482942 C>G maps to NM_015908.5 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr7:100482942 C>G maps to NM_015908.5 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr9:111670655 C>T maps to NM_003640.3 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr9:111670655 C>T maps to NM_003640.3 V463V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chrX:100177938 C>G maps to ENST00000328526 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chrX:100177938 C>G maps to ENST00000328526 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:15287294 C>T maps to NM_201628.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:15287294 C>T maps to NM_201628.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:36921786 C>G did not map to a codon.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:36921786 C>G did not map to a codon.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:37271711 C>T maps to NM_000831.3 T769T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:37271711 C>T maps to NM_000831.3 T769T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:45793380 C>T maps to NM_032756.2 C187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:45793380 C>T maps to NM_032756.2 C187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:46073824 C>G maps to NM_002482.3 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:46073824 C>G maps to NM_002482.3 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:64936609 G>A maps to ENST00000371073 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:64936609 G>A maps to ENST00000371073 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:147091316 C>T maps to NM_004326.2 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:147091316 C>T maps to NM_004326.2 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:152276144 G>A maps to NM_002016.1 H3739H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:152276144 G>A maps to NM_002016.1 H3739H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:152283116 T>C maps to NM_002016.1 Q1415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:152283116 T>C maps to NM_002016.1 Q1415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:156504952 G>T did not map to a codon.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:156504952 G>T did not map to a codon.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:161487823 C>T maps to NM_001136219.1 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:161487823 C>T maps to NM_001136219.1 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:161953787 C>A maps to ENST00000451379 E645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:161953787 C>A maps to ENST00000451379 E645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:169364285 C>T maps to ENST00000367806 *510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:169364285 C>T maps to ENST00000367806 *510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:172376928 C>A maps to ENST00000359070 S857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:172376928 C>A maps to ENST00000359070 S857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:204124946 C>A did not map to a codon.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:204124946 C>A did not map to a codon.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:229770965 C>T maps to NM_014777.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr1:229770965 C>T maps to NM_014777.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr10:124336112 C>A maps to ENST00000368915 S161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr10:124336112 C>A maps to ENST00000368915 S161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr11:607243 G>A maps to ENST00000264555 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr11:607243 G>A maps to ENST00000264555 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr11:65308357 G>A maps to NM_001130144.2 G987G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr11:65308357 G>A maps to NM_001130144.2 G987G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr11:67789311 C>T maps to NM_001161473.1 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr11:67789311 C>T maps to NM_001161473.1 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr11:70176373 C>G maps to NM_003626.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr11:70176373 C>G maps to NM_003626.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr12:8211881 A>T maps to NM_004054.2 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr12:8211881 A>T maps to NM_004054.2 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr13:113748881 C>G maps to NM_001112732.1 S1060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr13:113748881 C>G maps to NM_001112732.1 S1060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr14:24531702 C>G maps to NM_138360.3 S832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr14:24531702 C>G maps to NM_138360.3 S832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr15:55677907 G>T maps to ENST00000442196 S22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr15:55677907 G>T maps to ENST00000442196 S22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr16:2522334 C>G maps to NM_006181.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr16:2522334 C>G maps to NM_006181.1 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr16:19838427 C>T maps to NM_153208.1 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr16:19838427 C>T maps to NM_153208.1 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr16:28847378 G>A maps to NM_148414.1 Q1007Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr16:28847378 G>A maps to NM_148414.1 Q1007Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr16:52473777 G>A maps to ENST00000407228 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr16:52473777 G>A maps to ENST00000407228 Q364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr16:67203678 C>T maps to NM_001040667.2 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr16:67203678 C>T maps to NM_001040667.2 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr16:70575646 A>G maps to NM_012426.4 E381E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr16:70575646 A>G maps to NM_012426.4 E381E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr17:27963168 G>A maps to NM_033389.2 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr17:27963168 G>A maps to NM_033389.2 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr17:28296202 G>A maps to NM_198529.3 K195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr17:28296202 G>A maps to NM_198529.3 K195K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr17:42228330 G>A maps to NM_024032.3 Q409Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr17:42228330 G>A maps to NM_024032.3 Q409Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr17:72367968 C>T maps to ENST00000440684 Q1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr17:72367968 C>T maps to ENST00000440684 Q1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr19:9049323 G>A maps to NM_024690.2 V10769V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr19:9049323 G>A maps to NM_024690.2 V10769V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr19:15349768 G>A maps to NM_058243.2 L1269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr19:15349768 G>A maps to NM_058243.2 L1269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr19:15350614 G>A maps to NM_058243.2 S1100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr19:15350614 G>A maps to NM_058243.2 S1100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr19:35516978 C>T maps to NM_020895.3 H703H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr19:35516978 C>T maps to NM_020895.3 H703H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr19:45395689 C>A maps to NM_006114.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr19:45395689 C>A maps to NM_006114.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr19:45540981 C>T maps to ENST00000221452 F558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr19:45540981 C>T maps to ENST00000221452 F558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr2:11911610 C>T maps to ENST00000396099 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr2:11911610 C>T maps to ENST00000396099 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr2:209191021 C>T maps to NM_015040.3 Q1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr2:209191021 C>T maps to NM_015040.3 Q1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr2:242415336 C>T maps to NM_014808.2 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr2:242415336 C>T maps to NM_014808.2 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr20:13839916 G>A maps to NM_025229.1 G603G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr20:13839916 G>A maps to NM_025229.1 G603G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr22:41077103 C>A maps to NM_005297.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr22:41077103 C>A maps to NM_005297.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr22:50500012 C>T maps to NM_015166.3 *378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr22:50500012 C>T maps to NM_015166.3 *378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr3:48505261 C>T maps to NM_130384.1 Q622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr3:48505261 C>T maps to NM_130384.1 Q622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr3:105258903 G>A maps to NM_001627.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr3:105258903 G>A maps to NM_001627.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr3:120998726 C>T maps to NM_014980.2 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr3:120998726 C>T maps to NM_014980.2 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr3:122003857 G>A maps to NM_001178065.1 G1029G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr3:122003857 G>A maps to NM_001178065.1 G1029G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr3:129293181 G>A maps to NM_015103.2 H894H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr3:129293181 G>A maps to NM_015103.2 H894H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr3:145917611 A>G maps to NM_020353.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr3:145917611 A>G maps to NM_020353.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr4:52861474 A>G maps to NM_001024611.1 Y571Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr4:52861474 A>G maps to NM_001024611.1 Y571Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr5:16177894 G>T maps to NM_001102562.1 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr5:16177894 G>T maps to NM_001102562.1 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr5:49706780 G>A maps to NM_198449.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr5:49706780 G>A maps to NM_198449.2 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr5:140590344 C>G maps to NM_018932.3 G622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr5:140590344 C>G maps to NM_018932.3 G622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr6:38819386 C>T maps to ENST00000327475 F1789F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr6:38819386 C>T maps to ENST00000327475 F1789F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr6:129950551 T>C maps to NM_033515.2 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr6:129950551 T>C maps to NM_033515.2 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr6:167728906 G>A maps to NM_018974.3 Q447Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr6:167728906 G>A maps to NM_018974.3 Q447Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr7:4862157 G>A maps to NM_018059.4 C494C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr7:4862157 G>A maps to NM_018059.4 C494C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr7:104752437 C>G maps to NM_182931.2 S1412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr7:104752437 C>G maps to NM_182931.2 S1412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr7:120590961 A>G maps to NM_019071.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr7:120590961 A>G maps to NM_019071.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr8:62555449 G>A maps to NM_004318.3 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr8:62555449 G>A maps to NM_004318.3 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr8:121222115 G>A maps to NM_021110.1 E481E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr8:121222115 G>A maps to NM_021110.1 E481E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr8:121292243 C>T maps to NM_021110.1 P1184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr8:121292243 C>T maps to NM_021110.1 P1184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr8:144946382 G>A maps to NM_031308.1 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr8:144946382 G>A maps to NM_031308.1 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr8:144991526 C>G maps to NM_201380.2 V4291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr8:144991526 C>G maps to NM_201380.2 V4291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr8:145096193 G>A maps to NM_198572.2 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr8:145096193 G>A maps to NM_198572.2 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr8:145662238 T>C maps to NM_013432.4 E597E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr8:145662238 T>C maps to NM_013432.4 E597E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr9:16419592 G>A maps to NM_017637.5 D898D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr9:16419592 G>A maps to NM_017637.5 D898D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr9:27056420 A>G maps to NM_025103.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr9:27056420 A>G maps to NM_025103.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr9:93375944 G>A maps to NM_017594.3 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chr9:93375944 G>A maps to NM_017594.3 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chrX:83128669 G>A maps to NM_021118.1 K318K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7086-01A-11D-2078-08 chrX:83128669 G>A maps to NM_021118.1 K318K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr1:1152945 G>A maps to NM_016176.3 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr1:1152945 G>A maps to NM_016176.3 F345F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr1:43909377 G>A maps to NM_015284.2 L2013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr1:43909377 G>A maps to NM_015284.2 L2013L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr1:144618115 G>T maps to NM_001037675.2 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr1:144618115 G>T maps to NM_001037675.2 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr1:186275988 G>T maps to NM_005807.3 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr1:186275988 G>T maps to NM_005807.3 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr1:198719737 C>T maps to ENST00000271610 L1064L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr1:198719737 C>T maps to ENST00000271610 L1064L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr1:245775204 C>T maps to NM_018012.3 D675D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr1:245775204 C>T maps to NM_018012.3 D675D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr10:70333693 C>T maps to NM_030625.2 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr10:70333693 C>T maps to NM_030625.2 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr10:91532578 A>G maps to ENST00000416354 S1822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr10:91532578 A>G maps to ENST00000416354 S1822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr11:9435862 C>T maps to NM_006391.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr11:9435862 C>T maps to NM_006391.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr11:18159570 C>T maps to NM_054031.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr11:18159570 C>T maps to NM_054031.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr12:5744498 G>A maps to ENST00000356134 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr12:5744498 G>A maps to ENST00000356134 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr12:20893266 C>T maps to NM_017435.4 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr12:20893266 C>T maps to NM_017435.4 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr12:51080374 G>A maps to NM_173602.2 W487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr12:51080374 G>A maps to NM_173602.2 W487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr14:39565169 T>C maps to NM_006364.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr14:39565169 T>C maps to NM_006364.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr14:75199487 T>A maps to NM_015962.4 Y140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr14:75199487 T>A maps to NM_015962.4 Y140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr16:20871624 G>A maps to NM_173475.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr16:20871624 G>A maps to NM_173475.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr17:34893501 G>A maps to NM_178517.3 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr17:34893501 G>A maps to NM_178517.3 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr19:18232572 G>A maps to NM_015016.1 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr19:18232572 G>A maps to NM_015016.1 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr19:34895681 G>T maps to NM_032346.1 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr19:34895681 G>T maps to NM_032346.1 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr2:179648931 C>T maps to NM_133378.4 Q880Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr2:179648931 C>T maps to NM_133378.4 Q880Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr2:228884678 C>T maps to NM_001142644.1 Q297Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr2:228884678 C>T maps to NM_001142644.1 Q297Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr20:61512689 G>A maps to NM_033081.2 Q1540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr20:61512689 G>A maps to NM_033081.2 Q1540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr20:62597654 G>T maps to NM_020713.1 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr20:62597654 G>T maps to NM_020713.1 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr3:56468820 G>T maps to ENST00000460849 S72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr3:56468820 G>T maps to ENST00000460849 S72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr3:140251314 C>A maps to NM_022131.2 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr3:140251314 C>A maps to NM_022131.2 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr3:184043327 G>T maps to NM_001194947.1 E1015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr3:184043327 G>T maps to NM_001194947.1 E1015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr3:186392969 C>T maps to NM_000412.2 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr3:186392969 C>T maps to NM_000412.2 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr4:48622738 G>A maps to NM_015030.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr4:48622738 G>A maps to NM_015030.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr4:84352816 C>T maps to NM_133636.2 K765K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr4:84352816 C>T maps to NM_133636.2 K765K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr4:85707146 T>C maps to NM_014991.4 K1349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr4:85707146 T>C maps to NM_014991.4 K1349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr4:88903946 G>T maps to NM_001040058.1 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr4:88903946 G>T maps to NM_001040058.1 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr5:36152986 G>C maps to NM_005983.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr5:36152986 G>C maps to NM_005983.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr5:73205673 C>T maps to NM_001080479.2 H1533H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr5:73205673 C>T maps to NM_001080479.2 H1533H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr5:96121616 G>A maps to NM_016442.3 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr5:96121616 G>A maps to NM_016442.3 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr6:26045673 C>G maps to NM_003531.2 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr6:26045673 C>G maps to NM_003531.2 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr6:62604556 C>A maps to NM_152688.2 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr6:62604556 C>A maps to NM_152688.2 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr6:79607894 A>G maps to NM_001010844.1 K209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr6:79607894 A>G maps to NM_001010844.1 K209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr7:50534958 C>A maps to NM_000790.3 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr7:50534958 C>A maps to NM_000790.3 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr7:63720696 A>G maps to NM_153363.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr7:63720696 A>G maps to NM_153363.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr9:36599429 C>T maps to NM_014791.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr9:36599429 C>T maps to NM_014791.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr9:128003179 G>C maps to NM_005347.4 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr9:128003179 G>C maps to NM_005347.4 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr9:131221881 C>T maps to NM_153435.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr9:131221881 C>T maps to NM_153435.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr9:136234195 G>A maps to NM_033161.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7219-01A-11D-2012-08 chr9:136234195 G>A maps to NM_033161.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr13:37679303 G>A maps to NM_145203.5 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr13:37679303 G>A maps to NM_145203.5 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr13:99042296 C>A maps to NM_005766.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr13:99042296 C>A maps to NM_005766.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr14:71205083 G>A maps to NM_033141.2 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr14:71205083 G>A maps to NM_033141.2 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr15:50215662 A>C maps to NM_024837.2 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr15:50215662 A>C maps to NM_024837.2 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr16:1815177 C>T maps to NM_015133.3 P814P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr16:1815177 C>T maps to NM_015133.3 P814P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr16:67213450 C>G maps to NM_001040715.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr16:67213450 C>G maps to NM_001040715.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr17:4575882 T>G maps to ENST00000301396 P945P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr17:4575882 T>G maps to ENST00000301396 P945P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr19:7531841 C>T maps to NM_001130955.1 P793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr19:7531841 C>T maps to NM_001130955.1 P793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr19:14508887 C>T maps to NM_078481.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr19:14508887 C>T maps to NM_078481.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr19:17373675 C>T maps to NM_031941.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr19:17373675 C>T maps to NM_031941.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr19:56466996 C>T maps to NM_176811.2 Q525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr19:56466996 C>T maps to NM_176811.2 Q525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr2:21233486 G>A maps to NM_000384.2 R2085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr2:21233486 G>A maps to NM_000384.2 R2085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr2:191843714 G>A maps to NM_007315.3 G580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr2:191843714 G>A maps to NM_007315.3 G580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr2:197763048 G>A maps to NM_024989.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr2:197763048 G>A maps to NM_024989.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr20:47863941 C>T maps to NM_021035.2 K1873K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr20:47863941 C>T maps to NM_021035.2 K1873K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr4:126372349 C>T maps to NM_024582.4 V3393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr4:126372349 C>T maps to NM_024582.4 V3393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr4:156277011 C>T maps to NM_001039580.1 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr4:156277011 C>T maps to NM_001039580.1 K382K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr4:177146411 C>T did not map to a codon.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr4:177146411 C>T did not map to a codon.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr5:98218908 T>C maps to NM_001270.2 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr5:98218908 T>C maps to NM_001270.2 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr5:177548576 C>T maps to NM_015111.1 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr5:177548576 C>T maps to NM_015111.1 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr6:46787387 C>G maps to NM_005588.2 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr6:46787387 C>G maps to NM_005588.2 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chrX:51238819 C>T maps to NM_018159.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chrX:51238819 C>T maps to NM_018159.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chrX:128615128 G>A maps to NM_003069.3 R751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chrX:128615128 G>A maps to NM_003069.3 R751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chrX:152226305 A>G maps to NM_013364.4 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6515-01A-21D-1870-08 chrX:152226305 A>G maps to NM_013364.4 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:900537 C>T maps to NM_198317.2 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:900537 C>T maps to NM_198317.2 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:2103807 C>T maps to NM_002744.4 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:2103807 C>T maps to NM_002744.4 I422I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:6642210 C>T maps to NM_005341.2 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:6642210 C>T maps to NM_005341.2 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:10166446 T>G maps to NM_001105562.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:10166446 T>G maps to NM_001105562.2 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:11887265 C>T maps to ENST00000376496 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:11887265 C>T maps to ENST00000376496 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:12955429 C>T maps to NM_001039361.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:12955429 C>T maps to NM_001039361.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:16093893 C>T maps to NM_017556.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:16093893 C>T maps to NM_017556.2 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:19447896 G>A maps to ENST00000375267 F3309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:19447896 G>A maps to ENST00000375267 F3309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:19630781 G>A maps to NM_003689.2 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:19630781 G>A maps to NM_003689.2 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:26012974 G>A maps to NM_020379.2 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:26012974 G>A maps to NM_020379.2 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:26366379 G>A maps to NM_001004434.1 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:26366379 G>A maps to NM_001004434.1 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:27190365 G>A maps to NM_006142.3 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:27190365 G>A maps to NM_006142.3 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:32678089 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:32678089 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:32742007 G>A maps to ENST00000373562 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:32742007 G>A maps to ENST00000373562 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:41483464 G>A maps to NM_144990.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:41483464 G>A maps to NM_144990.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:43853230 G>A maps to NM_052877.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:43853230 G>A maps to NM_052877.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:45292234 G>C maps to NM_003738.4 A967A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:45292234 G>C maps to NM_003738.4 A967A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:47685628 C>T maps to ENST00000371883 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:47685628 C>T maps to ENST00000371883 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:52841196 G>A maps to NM_004153.3 S736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:52841196 G>A maps to NM_004153.3 S736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:62503684 C>A maps to NM_176877.2 P1332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:62503684 C>A maps to NM_176877.2 P1332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:75072543 C>T maps to NM_001002912.4 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:75072543 C>T maps to NM_001002912.4 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:100212951 G>A maps to NM_001013660.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:100212951 G>A maps to NM_001013660.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:110051360 G>A maps to NM_020703.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:110051360 G>A maps to NM_020703.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:110590434 A>T maps to NM_033088.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:110590434 A>T maps to NM_033088.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:111216579 G>A maps to NM_002232.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:111216579 G>A maps to NM_002232.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:119466121 C>T maps to ENST00000369429 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:119466121 C>T maps to ENST00000369429 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:150300843 C>T maps to NM_004698.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:150300843 C>T maps to NM_004698.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:152187528 C>T maps to NM_001009931.1 S2192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:152187528 C>T maps to NM_001009931.1 S2192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:152187633 G>A maps to NM_001009931.1 S2157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:152187633 G>A maps to NM_001009931.1 S2157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:152188176 G>A maps to NM_001009931.1 S1976S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:152188176 G>A maps to NM_001009931.1 S1976S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:155254457 C>T maps to NM_020897.1 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:155254457 C>T maps to NM_020897.1 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:156145016 C>T maps to NM_022367.3 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:156145016 C>T maps to NM_022367.3 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:156246879 G>A maps to NM_015327.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:156246879 G>A maps to NM_015327.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:156348149 C>T maps to NM_020407.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:156348149 C>T maps to NM_020407.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:156880482 G>A maps to NM_001080471.1 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:156880482 G>A maps to NM_001080471.1 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:158368956 G>A maps to NM_001004475.1 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:158368956 G>A maps to NM_001004475.1 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:158724700 G>A maps to NM_001005184.1 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:158724700 G>A maps to NM_001005184.1 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:159176032 C>T maps to NM_001122951.2 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:159176032 C>T maps to NM_001122951.2 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:177909753 C>T maps to NM_033127.2 R706R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:177909753 C>T maps to NM_033127.2 R706R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:182856370 C>A maps to NM_001357.4 S1205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:182856370 C>A maps to NM_001357.4 S1205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:193065759 G>A maps to NM_016066.3 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:193065759 G>A maps to NM_016066.3 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:196796105 G>A maps to NM_002113.2 W134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:196796105 G>A maps to NM_002113.2 W134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:198671528 G>A maps to ENST00000271610 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:198671528 G>A maps to ENST00000271610 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:203149597 C>T maps to NM_001276.2 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:203149597 C>T maps to NM_001276.2 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:204124206 G>A maps to NM_000537.3 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:204124206 G>A maps to NM_000537.3 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:205042323 G>A maps to NM_005076.3 G991G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:205042323 G>A maps to NM_005076.3 G991G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:205904873 C>T maps to NM_134325.2 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:205904873 C>T maps to NM_134325.2 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:206821331 G>A maps to NM_003582.2 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:206821331 G>A maps to NM_003582.2 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:213414909 T>G maps to NM_012424.3 G697G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:213414909 T>G maps to NM_012424.3 G697G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:216680457 C>T maps to NM_001438.2 Q400Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:216680457 C>T maps to NM_001438.2 Q400Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:220791839 C>T maps to NM_018650.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:220791839 C>T maps to NM_018650.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:222717465 G>A maps to NM_024746.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:222717465 G>A maps to NM_024746.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:228362982 C>T maps to NM_001010867.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:228362982 C>T maps to NM_001010867.2 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:230979404 G>A maps to NM_032800.2 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:230979404 G>A maps to NM_032800.2 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:235643459 G>A maps to ENST00000366599 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:235643459 G>A maps to ENST00000366599 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:237540663 C>T maps to NM_001035.2 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:237540663 C>T maps to NM_001035.2 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:237754052 G>A maps to NM_001035.2 P1307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:237754052 G>A maps to NM_001035.2 P1307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:237947404 C>G maps to NM_001035.2 P4131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:237947404 C>G maps to NM_001035.2 P4131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:243289828 T>C maps to NM_014812.2 E1559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:243289828 T>C maps to NM_014812.2 E1559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:247163358 C>T maps to NM_020394.3 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:247163358 C>T maps to NM_020394.3 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:247655079 C>T maps to NM_001004698.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:247655079 C>T maps to NM_001004698.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:247752020 G>A maps to NM_001001915.1 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:247752020 G>A maps to NM_001001915.1 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:248224681 G>A maps to NM_001004687.1 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:248224681 G>A maps to NM_001004687.1 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:5966445 C>T maps to NM_032807.3 C908C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:5966445 C>T maps to NM_032807.3 C908C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:16948289 C>T maps to NM_001081.3 Q2608Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:16948289 C>T maps to NM_001081.3 Q2608Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:26518693 C>T maps to NM_001134366.1 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:26518693 C>T maps to NM_001134366.1 F276F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:44052300 C>T maps to NM_001099284.1 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:44052300 C>T maps to NM_001099284.1 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:67862932 G>A maps to NM_013266.2 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:67862932 G>A maps to NM_013266.2 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:70190225 G>A maps to NM_001080449.1 S811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:70190225 G>A maps to NM_001080449.1 S811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:73570314 G>A maps to ENST00000398860 L3027L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:73570314 G>A maps to ENST00000398860 L3027L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:88260012 C>T maps to ENST00000342368 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:88260012 C>T maps to ENST00000342368 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:98157000 C>T maps to NM_012465.3 W442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:98157000 C>T maps to NM_012465.3 W442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:100179846 C>T maps to NM_000195.2 E604E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:100179846 C>T maps to NM_000195.2 E604E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:101163323 C>T maps to NM_002079.2 Q287Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:101163323 C>T maps to NM_002079.2 Q287Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:101824950 G>A maps to NM_001308.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:101824950 G>A maps to NM_001308.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:102249489 T>A maps to NM_015490.3 P998P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:102249489 T>A maps to NM_015490.3 P998P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:106970960 C>T maps to NM_014978.1 S776S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:106970960 C>T maps to NM_014978.1 S776S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:124345744 C>T maps to ENST00000368915 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr10:124345744 C>T maps to ENST00000368915 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:432044 G>A maps to NM_001012302.2 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:432044 G>A maps to NM_001012302.2 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:1643014 G>A maps to ENST00000359229 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:1643014 G>A maps to ENST00000359229 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:1643053 G>A maps to ENST00000359229 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:1643053 G>A maps to ENST00000359229 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:3681447 C>T maps to NM_004314.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:3681447 C>T maps to NM_004314.2 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:5012646 C>T maps to NM_021801.3 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:5012646 C>T maps to NM_021801.3 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:6472239 G>A maps to NM_033278.2 D584D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:6472239 G>A maps to NM_033278.2 D584D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:9917510 A>T maps to NM_030962.3 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:9917510 A>T maps to NM_030962.3 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:12257761 G>A maps to NM_014632.2 R678R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:12257761 G>A maps to NM_014632.2 R678R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:22364833 C>T maps to NM_020346.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:22364833 C>T maps to NM_020346.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:45274136 G>A maps to NM_020826.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:45274136 G>A maps to NM_020826.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:47256376 C>T maps to NM_000107.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:47256376 C>T maps to NM_000107.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:47650567 G>A maps to NM_014342.3 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:47650567 G>A maps to NM_014342.3 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:55135799 C>T maps to NM_001005275.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:55135799 C>T maps to NM_001005275.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:55652951 C>T maps to NM_032681.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:55652951 C>T maps to NM_032681.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:55798250 T>C maps to NM_001001921.1 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:55798250 T>C maps to NM_001001921.1 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:57254630 G>A maps to NM_003627.5 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:57254630 G>A maps to NM_003627.5 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:59132055 G>A maps to NM_001004729.1 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:59132055 G>A maps to NM_001004729.1 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:59610012 C>T maps to NM_005142.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:59610012 C>T maps to NM_005142.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:59612890 G>A maps to NM_005142.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:59612890 G>A maps to NM_005142.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:61583898 G>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:61583898 G>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:62655840 C>T maps to NM_001012661.1 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:62655840 C>T maps to NM_001012661.1 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:65633308 C>T maps to NM_025128.4 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:65633308 C>T maps to NM_025128.4 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:66319002 G>A maps to NM_001104.1 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:66319002 G>A maps to NM_001104.1 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:66391952 C>T maps to NM_006328.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:66391952 C>T maps to NM_006328.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:66460039 G>A maps to NM_006946.2 S1719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:66460039 G>A maps to NM_006946.2 S1719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:77937682 C>T maps to NM_080491.2 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:77937682 C>T maps to NM_080491.2 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:89902143 G>C maps to NM_005467.3 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:89902143 G>C maps to NM_005467.3 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:92624017 G>A maps to ENST00000298047 T4503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:92624017 G>A maps to ENST00000298047 T4503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:94129657 C>T maps to NM_016540.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:94129657 C>T maps to NM_016540.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:94230097 G>A maps to NM_017704.2 W80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:94230097 G>A maps to NM_017704.2 W80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:104878061 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:104878061 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:117301447 C>T maps to NM_020693.2 R1952R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:117301447 C>T maps to NM_020693.2 R1952R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:118111018 C>T maps to NM_198275.1 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:118111018 C>T maps to NM_198275.1 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:118390381 C>T maps to NM_001197104.1 F3732F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:118390381 C>T maps to NM_001197104.1 F3732F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:119052949 C>T maps to NM_024618.2 N834N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:119052949 C>T maps to NM_024618.2 N834N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:120347992 T>A maps to NM_015313.2 L1144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:120347992 T>A maps to NM_015313.2 L1144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:121008715 C>A maps to NM_005422.2 Y1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:121008715 C>A maps to NM_005422.2 Y1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:123887147 G>A maps to NM_001004462.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:123887147 G>A maps to NM_001004462.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:123894354 G>A maps to NM_001001953.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:123894354 G>A maps to NM_001001953.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:123900445 G>A maps to NM_001004464.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:123900445 G>A maps to NM_001004464.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:123901243 A>T maps to ENST00000375021 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:123901243 A>T maps to ENST00000375021 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:124829769 G>A maps to NM_025004.2 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:124829769 G>A maps to NM_025004.2 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:125267804 G>T maps to NM_022062.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:125267804 G>T maps to NM_022062.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:129802047 G>A maps to NM_020228.2 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:129802047 G>A maps to NM_020228.2 I412I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:134244921 C>T maps to NM_138342.3 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr11:134244921 C>T maps to NM_138342.3 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:2016672 G>A maps to NM_172364.4 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:2016672 G>A maps to NM_172364.4 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:2566792 G>A maps to NM_199460.2 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:2566792 G>A maps to NM_199460.2 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:6909312 G>A maps to NM_000616.4 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:6909312 G>A maps to NM_000616.4 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:6973917 C>T maps to NM_001098536.1 I759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:6973917 C>T maps to NM_001098536.1 I759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:8212049 C>T maps to NM_004054.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:8212049 C>T maps to NM_004054.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:10774548 G>A maps to NM_018423.2 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:10774548 G>A maps to NM_018423.2 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:11061285 G>A maps to NM_023920.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:11061285 G>A maps to NM_023920.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:39726013 A>G did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:39726013 A>G did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:39973416 C>T maps to NM_005164.3 W599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:39973416 C>T maps to NM_005164.3 W599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:41967304 C>T maps to NM_001164595.1 D908D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:41967304 C>T maps to NM_001164595.1 D908D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:44148205 C>T maps to NM_031292.3 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:44148205 C>T maps to NM_031292.3 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:46761091 G>A maps to NM_018976.4 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:46761091 G>A maps to NM_018976.4 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:47181733 G>A maps to NM_018018.4 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:47181733 G>A maps to NM_018018.4 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:48383558 G>A maps to NM_001844.4 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:48383558 G>A maps to NM_001844.4 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:49312667 G>A maps to NM_033124.4 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:49312667 G>A maps to NM_033124.4 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:49719906 C>T maps to NM_005480.3 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:49719906 C>T maps to NM_005480.3 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:50400384 G>A maps to NM_013277.3 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:50400384 G>A maps to NM_013277.3 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:50483705 C>T maps to NM_003076.4 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:50483705 C>T maps to NM_003076.4 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:53187988 G>A maps to ENST00000309505 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:53187988 G>A maps to ENST00000309505 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:53589184 C>T maps to NM_000889.1 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:53589184 C>T maps to NM_000889.1 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:54936456 C>T maps to NM_005337.4 F1124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:54936456 C>T maps to NM_005337.4 F1124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:54969815 G>T maps to NM_000924.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:54969815 G>T maps to NM_000924.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:56031406 C>T maps to NM_206899.1 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:56031406 C>T maps to NM_206899.1 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:56109966 C>T maps to NM_001487.3 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:56109966 C>T maps to NM_001487.3 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:56216452 A>G maps to NM_032364.5 H566H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:56216452 A>G maps to NM_032364.5 H566H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:56504216 G>T maps to NM_006191.2 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:56504216 G>T maps to NM_006191.2 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:56638204 G>A maps to NM_173595.3 R913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:56638204 G>A maps to NM_173595.3 R913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:57003657 G>A maps to NM_013449.3 R654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:57003657 G>A maps to NM_013449.3 R654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:57324257 G>A maps to NM_148897.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:57324257 G>A maps to NM_148897.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:57554759 C>T maps to NM_002332.2 H688H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:57554759 C>T maps to NM_002332.2 H688H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:57569839 C>T maps to NM_002332.2 T1314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:57569839 C>T maps to NM_002332.2 T1314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:64173778 C>T maps to NM_014254.1 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:64173778 C>T maps to NM_014254.1 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:70918332 G>A maps to NM_001109754.1 V2181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:70918332 G>A maps to NM_001109754.1 V2181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:75601547 G>A maps to NM_139137.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:75601547 G>A maps to NM_139137.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:78553042 C>T maps to NM_014903.4 L1616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:78553042 C>T maps to NM_014903.4 L1616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:81747118 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:81747118 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:85515604 C>T maps to NM_001079910.1 Q1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:85515604 C>T maps to NM_001079910.1 Q1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:99223029 C>T maps to NM_152788.3 Q996Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:99223029 C>T maps to NM_152788.3 Q996Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:104645323 T>A maps to NM_001093771.1 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:104645323 T>A maps to NM_001093771.1 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:108169093 G>A maps to NM_203436.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:108169093 G>A maps to NM_203436.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:109182303 G>A maps to NM_018984.3 P870P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:109182303 G>A maps to NM_018984.3 P870P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:109290807 C>T maps to NM_001917.4 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:109290807 C>T maps to NM_001917.4 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:109522851 C>T maps to NM_032663.3 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:109522851 C>T maps to NM_032663.3 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:121416882 G>A maps to NM_000545.5 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:121416882 G>A maps to NM_000545.5 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:123687372 G>A maps to NM_022782.2 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:123687372 G>A maps to NM_022782.2 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:124819763 G>A maps to NM_006312.4 Q2117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:124819763 G>A maps to NM_006312.4 Q2117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:133423716 C>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:133423716 C>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:21205186 G>A maps to NM_175605.3 K453K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:21205186 G>A maps to NM_175605.3 K453K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:23913424 G>A maps to NM_014363.4 F1530F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:23913424 G>A maps to NM_014363.4 F1530F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:23930132 G>A maps to NM_014363.4 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:23930132 G>A maps to NM_014363.4 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:61986526 G>A maps to NM_022843.3 Q569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:61986526 G>A maps to NM_022843.3 Q569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:73401256 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:73401256 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:75898413 C>T maps to ENST00000431480 Q719Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:75898413 C>T maps to ENST00000431480 Q719Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:78335134 G>A maps to ENST00000389459 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:78335134 G>A maps to ENST00000389459 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:78477473 C>T maps to ENST00000377211 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:78477473 C>T maps to ENST00000377211 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:113852536 G>A maps to ENST00000246505 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr13:113852536 G>A maps to ENST00000246505 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:20296254 C>T maps to NM_001004723.1 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:20296254 C>T maps to NM_001004723.1 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:20344869 C>T maps to NM_001005501.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:20344869 C>T maps to NM_001005501.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:20443770 C>A maps to NM_001005486.1 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:20443770 C>A maps to NM_001005486.1 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:20482830 C>T maps to NM_001004712.1 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:20482830 C>T maps to NM_001004712.1 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:20502833 G>A maps to NM_001004714.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:20502833 G>A maps to NM_001004714.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:20845879 G>A maps to NM_007110.4 P1918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:20845879 G>A maps to NM_007110.4 P1918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:23312535 C>T maps to NM_004995.2 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:23312535 C>T maps to NM_004995.2 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:23855232 C>T maps to NM_002471.3 E1689E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:23855232 C>T maps to NM_002471.3 E1689E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:24647313 C>T maps to NM_005132.2 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:24647313 C>T maps to NM_005132.2 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:24884779 C>T maps to NM_025081.2 L1275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:24884779 C>T maps to NM_025081.2 L1275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:31185182 C>T maps to ENST00000311943 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:31185182 C>T maps to ENST00000311943 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:31346826 G>A maps to NM_004086.2 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:31346826 G>A maps to NM_004086.2 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:31574595 G>A maps to NM_015382.2 A2464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:31574595 G>A maps to NM_015382.2 A2464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:35595979 C>T maps to NM_014672.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:35595979 C>T maps to NM_014672.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:39717157 C>T maps to NM_054024.3 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:39717157 C>T maps to NM_054024.3 F460F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:59113413 G>A maps to NM_016651.5 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:59113413 G>A maps to NM_016651.5 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:65453805 C>T maps to NM_002028.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:65453805 C>T maps to NM_002028.3 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:67859924 G>A maps to NM_016445.1 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:67859924 G>A maps to NM_016445.1 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:73490961 C>T maps to NM_021260.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:73490961 C>T maps to NM_021260.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:74411449 G>A maps to NM_152445.1 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:74411449 G>A maps to NM_152445.1 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:74874629 G>A maps to NM_001105579.1 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:74874629 G>A maps to NM_001105579.1 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:92600676 C>T maps to NM_017437.1 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:92600676 C>T maps to NM_017437.1 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:94041486 G>A maps to ENST00000393153 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:94041486 G>A maps to ENST00000393153 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:95030211 C>T maps to NM_006215.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:95030211 C>T maps to NM_006215.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:96152887 G>A maps to NM_004918.3 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:96152887 G>A maps to NM_004918.3 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:96707405 C>T maps to NM_000623.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:96707405 C>T maps to NM_000623.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:96730396 C>T maps to NM_000710.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:96730396 C>T maps to NM_000710.2 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:102675277 G>T maps to ENST00000454394 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:102675277 G>T maps to ENST00000454394 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:103566783 C>T maps to NM_001077594.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:103566783 C>T maps to NM_001077594.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:105408932 G>A maps to NM_138420.2 S4285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:105408932 G>A maps to NM_138420.2 S4285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:105417194 G>A maps to NM_138420.2 S1531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:105417194 G>A maps to NM_138420.2 S1531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:105418184 G>A maps to NM_138420.2 S1201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr14:105418184 G>A maps to NM_138420.2 S1201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:22368757 C>T maps to NM_001004719.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:22368757 C>T maps to NM_001004719.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:24922336 C>T maps to NM_018958.2 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:24922336 C>T maps to NM_018958.2 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:28116343 G>A maps to NM_000275.2 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:28116343 G>A maps to NM_000275.2 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:28358820 G>A maps to NM_004667.4 L4639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:28358820 G>A maps to NM_004667.4 L4639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:34072525 C>T maps to NM_001036.3 T3084T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:34072525 C>T maps to NM_001036.3 T3084T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:40659296 G>A maps to NM_033510.1 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:40659296 G>A maps to NM_033510.1 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:40751118 C>T maps to NM_014952.3 H152H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:40751118 C>T maps to NM_014952.3 H152H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:40917520 C>T maps to NM_170589.3 Q1713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:40917520 C>T maps to NM_170589.3 Q1713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:41191636 C>T maps to NM_020857.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:41191636 C>T maps to NM_020857.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:42149209 C>T maps to ENST00000320955 Q2883Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:42149209 C>T maps to ENST00000320955 Q2883Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:42192956 G>A maps to NM_139265.3 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:42192956 G>A maps to NM_139265.3 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:43815392 G>A maps to ENST00000382031 Q812Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:43815392 G>A maps to ENST00000382031 Q812Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:44881480 G>A maps to NM_025137.3 L1625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:44881480 G>A maps to NM_025137.3 L1625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:45723008 A>G maps to NM_197955.1 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:45723008 A>G maps to NM_197955.1 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:48058128 C>T maps to NM_153618.1 H497H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:48058128 C>T maps to NM_153618.1 H497H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:48460948 A>T maps to NM_016132.3 Y83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:48460948 A>T maps to NM_016132.3 Y83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:49436469 C>T maps to NM_001143887.1 W67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:49436469 C>T maps to NM_001143887.1 W67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:51534992 C>T maps to NM_031226.2 W39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:51534992 C>T maps to NM_031226.2 W39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:59383307 C>T maps to ENST00000434298 S907S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:59383307 C>T maps to ENST00000434298 S907S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:69714071 C>T maps to NM_138555.1 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:69714071 C>T maps to NM_138555.1 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:72141212 G>T maps to ENST00000424560 T2341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:72141212 G>T maps to ENST00000424560 T2341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:73028231 C>A maps to NM_033028.3 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:73028231 C>A maps to NM_033028.3 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:73028237 C>T maps to NM_033028.3 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:73028237 C>T maps to NM_033028.3 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:75702497 G>A maps to NM_001145357.1 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:75702497 G>A maps to NM_001145357.1 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:77906817 G>A maps to NM_032808.5 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:77906817 G>A maps to NM_032808.5 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:79750222 G>A maps to NM_015206.2 K578K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:79750222 G>A maps to NM_015206.2 K578K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:83331551 G>A maps to NM_004644.3 S890S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:83331551 G>A maps to NM_004644.3 S890S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:85382229 G>T maps to NM_020778.4 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:85382229 G>T maps to NM_020778.4 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:819553 C>T maps to NM_001025190.1 G1012G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:819553 C>T maps to NM_001025190.1 G1012G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:830221 C>T maps to NM_001025190.1 W260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:830221 C>T maps to NM_001025190.1 W260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:863383 C>T maps to NM_001013638.1 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:863383 C>T maps to NM_001013638.1 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:2049626 G>A maps to ENST00000431526 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:2049626 G>A maps to ENST00000431526 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:2158552 G>A maps to NM_001009944.2 A2205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:2158552 G>A maps to NM_001009944.2 A2205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:2546622 C>T maps to ENST00000434757 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:2546622 C>T maps to ENST00000434757 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:2946650 C>T maps to NM_138439.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:2946650 C>T maps to NM_138439.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:3079403 C>T maps to NM_001103175.1 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:3079403 C>T maps to NM_001103175.1 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:3613074 G>A maps to ENST00000448023 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:3613074 G>A maps to ENST00000448023 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:5055946 G>A maps to NM_014692.1 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:5055946 G>A maps to NM_014692.1 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:5058636 G>A maps to NM_014692.1 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:5058636 G>A maps to NM_014692.1 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:10851748 C>T maps to NM_002484.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:10851748 C>T maps to NM_002484.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:10989223 C>T maps to NM_000246.3 C46C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:10989223 C>T maps to NM_000246.3 C46C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:12136910 C>T maps to NM_032167.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:12136910 C>T maps to NM_032167.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:15705497 G>A maps to NM_014647.3 Q1190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:15705497 G>A maps to NM_014647.3 Q1190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:18823384 C>T maps to ENST00000389467 L3563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:18823384 C>T maps to ENST00000389467 L3563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:19236020 C>T maps to NM_016524.2 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:19236020 C>T maps to NM_016524.2 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:20487016 C>T maps to NM_001010845.2 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:20487016 C>T maps to NM_001010845.2 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:21213520 C>T maps to NM_003460.1 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:21213520 C>T maps to NM_003460.1 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:23569514 C>T maps to ENST00000219638 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:23569514 C>T maps to ENST00000219638 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:28617419 G>A maps to NM_177529.1 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:28617419 G>A maps to NM_177529.1 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:28617425 G>A maps to NM_177529.1 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:28617425 G>A maps to NM_177529.1 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:29675975 C>T maps to NM_003123.3 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:29675975 C>T maps to NM_003123.3 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:30998162 C>T maps to NM_025193.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:30998162 C>T maps to NM_025193.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:31046324 C>T maps to NM_004604.3 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:31046324 C>T maps to NM_004604.3 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:31421726 C>T maps to ENST00000444228 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:31421726 C>T maps to ENST00000444228 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:54319186 C>T maps to NM_024336.2 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:54319186 C>T maps to NM_024336.2 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:55362876 C>T maps to NM_024335.2 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:55362876 C>T maps to NM_024335.2 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:57088698 C>T maps to NM_032206.3 F1181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:57088698 C>T maps to NM_032206.3 F1181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:57151427 C>T maps to NM_152727.5 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:57151427 C>T maps to NM_152727.5 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:65006864 T>C maps to NM_001797.2 K444K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:65006864 T>C maps to NM_001797.2 K444K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:67328008 C>T maps to NM_001100915.1 K552K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:67328008 C>T maps to NM_001100915.1 K552K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:67701383 C>T maps to NM_001012984.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:67701383 C>T maps to NM_001012984.2 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:77910305 C>T maps to NM_020927.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:77910305 C>T maps to NM_020927.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:78458950 C>T maps to NM_016373.1 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:78458950 C>T maps to NM_016373.1 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:81045702 C>T maps to NM_001100624.1 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:81045702 C>T maps to NM_001100624.1 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:81134880 C>T maps to NM_052892.3 E2408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:81134880 C>T maps to NM_052892.3 E2408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:84256560 G>A maps to NM_172347.2 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:84256560 G>A maps to NM_172347.2 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:85953823 C>T maps to NM_002163.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:85953823 C>T maps to NM_002163.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:89764656 G>A maps to NM_152339.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr16:89764656 G>A maps to NM_152339.3 L120L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-D6-6516-01A-11D-1870-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-D6-6516-01A-11D-1870-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:915170 C>T maps to NM_021962.2 E672E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:915170 C>T maps to NM_021962.2 E672E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:1183396 G>A maps to NM_172367.2 E34E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:1183396 G>A maps to NM_172367.2 E34E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:1584902 G>A maps to NM_006445.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:1584902 G>A maps to NM_006445.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:2323365 G>A maps to NM_024086.3 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:2323365 G>A maps to NM_024086.3 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:3118955 C>T maps to NM_014565.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:3118955 C>T maps to NM_014565.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:3980239 G>A maps to NM_015113.3 S1011S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:3980239 G>A maps to NM_015113.3 S1011S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:5323604 C>T maps to NM_001033002.3 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:5323604 C>T maps to NM_001033002.3 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:5392533 C>T maps to NM_024039.1 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:5392533 C>T maps to NM_024039.1 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:10205017 C>T maps to NM_003802.2 E1890E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:10205017 C>T maps to NM_003802.2 E1890E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:10358388 G>A maps to NM_017533.2 F768F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:10358388 G>A maps to NM_017533.2 F768F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:10369996 C>T maps to NM_017533.2 K22K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:10369996 C>T maps to NM_017533.2 K22K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:10408288 G>T maps to NM_005963.3 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:10408288 G>T maps to NM_005963.3 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:10432159 G>A maps to NM_017534.5 T1197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:10432159 G>A maps to NM_017534.5 T1197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:10450896 G>A maps to NM_017534.5 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:10450896 G>A maps to NM_017534.5 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:17116980 C>T maps to NM_144997.5 E576E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:17116980 C>T maps to NM_144997.5 E576E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:18045391 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:18045391 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:19235286 C>T maps to NM_014964.4 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:19235286 C>T maps to NM_014964.4 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:26881399 G>A maps to NM_033198.3 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:26881399 G>A maps to NM_033198.3 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:26902185 G>A maps to NM_005165.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:26902185 G>A maps to NM_005165.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:29548870 C>T maps to NM_001042492.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:29548870 C>T maps to NM_001042492.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:33433485 C>T maps to NM_002878.3 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:33433485 C>T maps to NM_002878.3 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:33679467 C>T maps to NM_152270.3 R871R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:33679467 C>T maps to NM_152270.3 R871R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:38145045 C>T maps to NM_002809.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:38145045 C>T maps to NM_002809.2 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:39140174 C>T maps to NM_182497.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:39140174 C>T maps to NM_182497.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:39740511 C>T maps to NM_000526.4 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:39740511 C>T maps to NM_000526.4 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:39740537 G>A maps to NM_000526.4 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:39740537 G>A maps to NM_000526.4 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:40556779 G>A maps to NM_012232.5 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:40556779 G>A maps to NM_012232.5 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:41170068 C>T maps to NM_006373.3 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:41170068 C>T maps to NM_006373.3 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:41605895 G>A maps to NM_001079675.1 Y482Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:41605895 G>A maps to NM_001079675.1 Y482Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:47797714 C>T maps to NM_030802.3 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:47797714 C>T maps to NM_030802.3 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:51901497 G>A maps to NM_032559.4 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:51901497 G>A maps to NM_032559.4 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:56285487 G>A maps to NM_017777.3 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:56285487 G>A maps to NM_017777.3 F381F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:56664946 C>T maps to ENST00000240361 W934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:56664946 C>T maps to ENST00000240361 W934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:58740466 C>T maps to NM_003620.3 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:58740466 C>T maps to NM_003620.3 R458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:62479089 G>A maps to NM_007215.3 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:62479089 G>A maps to NM_007215.3 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:64222174 G>A maps to NM_000042.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:64222174 G>A maps to NM_000042.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:66352843 C>T maps to NM_014960.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:66352843 C>T maps to NM_014960.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:74621570 G>A maps to NM_018414.3 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:74621570 G>A maps to NM_018414.3 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:76447631 G>A maps to ENST00000389840 F3537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:76447631 G>A maps to ENST00000389840 F3537F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:78319832 C>T maps to NM_020914.4 Y2615Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:78319832 C>T maps to NM_020914.4 Y2615Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:78332093 C>T maps to NM_020914.4 T3672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:78332093 C>T maps to NM_020914.4 T3672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:79234187 G>A maps to NM_001037984.1 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:79234187 G>A maps to NM_001037984.1 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:79612448 C>T maps to NM_031945.3 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:79612448 C>T maps to NM_031945.3 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:80019149 G>A maps to NM_022156.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:80019149 G>A maps to NM_022156.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:80046904 G>A maps to NM_004104.4 A748A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:80046904 G>A maps to NM_004104.4 A748A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:3534552 G>A maps to NM_004746.2 F706F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:3534552 G>A maps to NM_004746.2 F706F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:6239846 G>A maps to NM_173464.3 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:6239846 G>A maps to NM_173464.3 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:9258556 C>T maps to NM_015208.3 S1764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:9258556 C>T maps to NM_015208.3 S1764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:9570372 A>T maps to NM_001042388.1 L452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:9570372 A>T maps to NM_001042388.1 L452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:13884842 G>A maps to NM_000529.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:13884842 G>A maps to NM_000529.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:19995653 C>T maps to NM_172241.2 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:19995653 C>T maps to NM_172241.2 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:21001408 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:21001408 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:25570167 A>G maps to NM_001792.3 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:25570167 A>G maps to NM_001792.3 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:33704510 G>A maps to NM_012319.3 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:33704510 G>A maps to NM_012319.3 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:44561203 C>T maps to NM_016427.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:44561203 C>T maps to NM_016427.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:50866164 G>A maps to NM_005215.3 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:50866164 G>A maps to NM_005215.3 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:59912004 C>T maps to NM_020854.3 I543I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:59912004 C>T maps to NM_020854.3 I543I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:74154068 G>A maps to ENST00000443185 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:74154068 G>A maps to ENST00000443185 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:77464882 C>T maps to NM_004715.3 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr18:77464882 C>T maps to NM_004715.3 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:806555 G>A maps to NM_002819.4 E373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:806555 G>A maps to NM_002819.4 E373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:1056929 C>T maps to NM_019112.3 L1537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:1056929 C>T maps to NM_019112.3 L1537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:2096976 G>T maps to NM_001039846.1 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:2096976 G>T maps to NM_001039846.1 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:3977900 G>A maps to NM_001961.3 I661I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:3977900 G>A maps to NM_001961.3 I661I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:4155014 C>T maps to NM_032607.1 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:4155014 C>T maps to NM_032607.1 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:4697573 C>T maps to ENST00000357909 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:4697573 C>T maps to ENST00000357909 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:7830110 C>T maps to NM_014257.4 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:7830110 C>T maps to NM_014257.4 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:9068059 C>T maps to NM_024690.2 W6462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:9068059 C>T maps to NM_024690.2 W6462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:9090941 G>T maps to NM_024690.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:9090941 G>T maps to NM_024690.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:9453077 G>A maps to NM_032497.1 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:9453077 G>A maps to NM_032497.1 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:9489657 A>G maps to NM_001172651.1 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:9489657 A>G maps to NM_001172651.1 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:10428228 C>T maps to NM_133452.2 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:10428228 C>T maps to NM_133452.2 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:11526778 C>T maps to NM_001161616.1 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:11526778 C>T maps to NM_001161616.1 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:11728613 T>C maps to NM_145295.3 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:11728613 T>C maps to NM_145295.3 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:12502623 A>C maps to NM_001080821.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:12502623 A>C maps to NM_001080821.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:13223746 G>A maps to NM_001136035.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:13223746 G>A maps to NM_001136035.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:18182997 G>A maps to NM_005535.1 N315N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:18182997 G>A maps to NM_005535.1 N315N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:18548555 G>A maps to NM_016368.4 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:18548555 G>A maps to NM_016368.4 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:22363930 G>A maps to NM_001001411.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:22363930 G>A maps to NM_001001411.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:29698649 C>T maps to NM_006003.2 W210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:29698649 C>T maps to NM_006003.2 W210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:33493155 G>A maps to NM_033103.4 Q368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:33493155 G>A maps to NM_033103.4 Q368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:35175541 C>T maps to ENST00000221282 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:35175541 C>T maps to ENST00000221282 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:35449807 T>C maps to NM_175872.4 K317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:35449807 T>C maps to NM_175872.4 K317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:35715961 G>A maps to NM_152481.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:35715961 G>A maps to NM_152481.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:36353413 G>A maps to NM_199180.2 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:36353413 G>A maps to NM_199180.2 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:36573967 C>T maps to NM_001083961.1 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:36573967 C>T maps to NM_001083961.1 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:38189303 G>A maps to NM_032689.4 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:38189303 G>A maps to NM_032689.4 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:38655372 C>G maps to NM_015073.1 G1345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:38655372 C>G maps to NM_015073.1 G1345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:38847128 C>T maps to NM_021185.4 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:38847128 C>T maps to NM_021185.4 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:38871606 C>T maps to NM_002812.4 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:38871606 C>T maps to NM_002812.4 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:39369800 G>A maps to NM_012237.3 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:39369800 G>A maps to NM_012237.3 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:39804665 G>A maps to NM_020862.1 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:39804665 G>A maps to NM_020862.1 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:39880373 C>T maps to NM_019088.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:39880373 C>T maps to NM_019088.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:40097948 C>A maps to NM_013268.2 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:40097948 C>A maps to NM_013268.2 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:40762854 G>A maps to NM_001626.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:40762854 G>A maps to NM_001626.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:42794461 C>T maps to NM_015125.3 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:42794461 C>T maps to NM_015125.3 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:43026181 G>A maps to NM_001712.4 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:43026181 G>A maps to NM_001712.4 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:44223318 G>A maps to NM_019612.3 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:44223318 G>A maps to NM_019612.3 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:44777199 G>A maps to NM_181756.1 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:44777199 G>A maps to NM_181756.1 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:44891416 G>A maps to NM_152354.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:44891416 G>A maps to NM_152354.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:44981194 G>A maps to NM_013256.3 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:44981194 G>A maps to NM_013256.3 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:46137674 C>T maps to NM_001193268.1 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:46137674 C>T maps to NM_001193268.1 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:47503695 C>A maps to NM_004491.4 A1417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:47503695 C>A maps to NM_004491.4 A1417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:47503752 C>T maps to NM_004491.4 F1436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:47503752 C>T maps to NM_004491.4 F1436F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:47570605 G>A maps to NM_015168.1 F973F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:47570605 G>A maps to NM_015168.1 F973F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:47597292 G>A maps to NM_015168.1 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:47597292 G>A maps to NM_015168.1 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:48255848 C>T maps to NM_015710.4 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:48255848 C>T maps to NM_015710.4 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:49387076 C>T maps to NM_003323.2 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:49387076 C>T maps to NM_003323.2 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:49514283 C>T maps to NM_006666.1 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:49514283 C>T maps to NM_006666.1 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:49539416 G>A maps to ENST00000391869 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:49539416 G>A maps to ENST00000391869 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:50780154 G>A maps to NM_001145809.1 R1274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:50780154 G>A maps to NM_001145809.1 R1274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:50957534 C>T maps to NM_004533.3 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:50957534 C>T maps to NM_004533.3 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:51051873 C>T maps to NM_001080457.1 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:51051873 C>T maps to NM_001080457.1 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:51133334 G>A maps to NM_001160329.1 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:51133334 G>A maps to NM_001160329.1 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:51361524 G>A maps to NM_001648.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:51361524 G>A maps to NM_001648.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:51563853 C>T maps to NM_015596.1 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:51563853 C>T maps to NM_015596.1 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:53015076 A>G maps to NM_001099694.1 K481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:53015076 A>G maps to NM_001099694.1 K481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:53668983 C>T maps to NM_024733.3 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:53668983 C>T maps to NM_024733.3 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:54444856 C>T maps to NM_031896.4 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:54444856 C>T maps to NM_031896.4 F186F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:56103956 G>A maps to NM_032836.2 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:56103956 G>A maps to NM_032836.2 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:56370045 C>T maps to NM_134444.4 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:56370045 C>T maps to NM_134444.4 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:56953820 G>A maps to ENST00000342634 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:56953820 G>A maps to ENST00000342634 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:57327571 G>A maps to NM_006210.2 D746D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:57327571 G>A maps to NM_006210.2 D746D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:57641803 C>T maps to NM_020903.2 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:57641803 C>T maps to NM_020903.2 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:57910605 C>T maps to NM_001172773.1 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:57910605 C>T maps to NM_001172773.1 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:58578349 G>A maps to NM_007134.1 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:58578349 G>A maps to NM_007134.1 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:59010013 C>T maps to NM_012254.2 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:59010013 C>T maps to NM_012254.2 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:59010863 G>A maps to NM_012254.2 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:59010863 G>A maps to NM_012254.2 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:3193184 G>A maps to ENST00000398659 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:3193184 G>A maps to ENST00000398659 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:5833794 C>T maps to NM_003108.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:5833794 C>T maps to NM_003108.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:11354482 C>T maps to NM_004850.3 K681K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:11354482 C>T maps to NM_004850.3 K681K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:11750975 C>T maps to NM_014668.3 P943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:11750975 C>T maps to NM_014668.3 P943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:11802336 G>A maps to NM_012344.3 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:11802336 G>A maps to NM_012344.3 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:20234790 G>A maps to NM_014713.4 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:20234790 G>A maps to NM_014713.4 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:21265244 C>T maps to NM_000384.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:21265244 C>T maps to NM_000384.2 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:24433774 G>A maps to NM_006277.2 S1377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:24433774 G>A maps to NM_006277.2 S1377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:26029097 C>T maps to NM_018263.4 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:26029097 C>T maps to NM_018263.4 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:27479725 G>A maps to NM_003459.4 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:27479725 G>A maps to NM_003459.4 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:27481074 G>A maps to NM_003459.4 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:27481074 G>A maps to NM_003459.4 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:27599206 C>T maps to NM_014748.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:27599206 C>T maps to NM_014748.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:43779472 T>A maps to ENST00000330266 K895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:43779472 T>A maps to ENST00000330266 K895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:48734517 T>G maps to NM_001135629.2 Y693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:48734517 T>G maps to NM_001135629.2 Y693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:48874000 T>C maps to NM_172311.2 G970G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:48874000 T>C maps to NM_172311.2 G970G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:48906535 G>A maps to NM_172311.2 G1168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:48906535 G>A maps to NM_172311.2 G1168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:49381543 G>A maps to NM_000145.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:49381543 G>A maps to NM_000145.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:51254988 C>T maps to ENST00000404971 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:51254988 C>T maps to ENST00000404971 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:55209755 C>T maps to NM_020532.4 E1085E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:55209755 C>T maps to NM_020532.4 E1085E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:60689545 G>A maps to NM_022893.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:60689545 G>A maps to NM_022893.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:69172544 G>A maps to NM_182536.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:69172544 G>A maps to NM_182536.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:71892331 C>T maps to NM_001130987.1 Q1739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:71892331 C>T maps to NM_001130987.1 Q1739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:85782638 A>T maps to NM_000821.4 Y231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:85782638 A>T maps to NM_000821.4 Y231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:96072817 C>T maps to NM_016044.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:96072817 C>T maps to NM_016044.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:97024781 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:97024781 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:98422127 G>A maps to NM_015348.1 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:98422127 G>A maps to NM_015348.1 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:102483018 C>T maps to NM_145686.2 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:102483018 C>T maps to NM_145686.2 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:105859280 C>T maps to NM_007227.3 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:105859280 C>T maps to NM_007227.3 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:111851061 A>C did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:111851061 A>C did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:128366401 C>T maps to ENST00000389524 F921F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:128366401 C>T maps to ENST00000389524 F921F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:131521445 C>T maps to NM_001105195.1 R601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:131521445 C>T maps to NM_001105195.1 R601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:137872795 G>A maps to ENST00000272643 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:137872795 G>A maps to ENST00000272643 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:169783743 G>A maps to NM_003742.2 T1180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:169783743 G>A maps to NM_003742.2 T1180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:177033898 G>A maps to NM_006898.4 K19K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:177033898 G>A maps to NM_006898.4 K19K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:179439623 G>A maps to NM_133378.4 T21177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:179439623 G>A maps to NM_133378.4 T21177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:179446508 G>A maps to NM_133378.4 F19594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:179446508 G>A maps to NM_133378.4 F19594F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:179486277 G>A maps to NM_133378.4 N12523N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:179486277 G>A maps to NM_133378.4 N12523N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:179590732 G>A maps to NM_133378.4 T5528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:179590732 G>A maps to NM_133378.4 T5528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:179594213 C>T maps to NM_133378.4 T4979T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:179594213 C>T maps to NM_133378.4 T4979T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:179605332 A>T maps to NM_133437.3 P4038P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:179605332 A>T maps to NM_133437.3 P4038P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:179616728 C>T maps to ENST00000375038 R3468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:179616728 C>T maps to ENST00000375038 R3468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:197729785 C>A maps to NM_024989.3 G596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:197729785 C>A maps to NM_024989.3 G596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:200173602 G>A maps to NM_001172509.1 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:200173602 G>A maps to NM_001172509.1 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:203776181 T>A maps to NM_018256.3 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:203776181 T>A maps to NM_018256.3 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:208486554 C>T maps to ENST00000272839 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:208486554 C>T maps to ENST00000272839 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:210559486 G>T maps to NM_002374.3 E865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:210559486 G>T maps to NM_002374.3 E865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:215610515 T>C maps to NM_000465.2 E580E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:215610515 T>C maps to NM_000465.2 E580E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:219292993 C>T maps to NM_007127.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:219292993 C>T maps to NM_007127.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:219536675 A>G maps to NM_022453.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:219536675 A>G maps to NM_022453.2 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:220422770 C>T maps to NM_015311.2 G1188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:220422770 C>T maps to NM_015311.2 G1188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:227985822 G>A maps to ENST00000396625 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:227985822 G>A maps to ENST00000396625 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:228883696 G>A maps to NM_001142644.1 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:228883696 G>A maps to NM_001142644.1 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:233899487 C>T maps to NM_005383.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:233899487 C>T maps to NM_005383.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:235404768 G>A maps to ENST00000339728 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:235404768 G>A maps to ENST00000339728 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:236708048 C>T maps to NM_001037131.1 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:236708048 C>T maps to NM_001037131.1 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:242576369 G>C maps to NM_015963.5 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr2:242576369 G>C maps to NM_015963.5 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:3679948 G>A maps to NM_023068.3 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:3679948 G>A maps to NM_023068.3 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:17475390 C>T maps to NM_001195.3 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:17475390 C>T maps to NM_001195.3 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:19665796 C>T maps to NM_020689.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:19665796 C>T maps to NM_020689.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:20208963 C>T maps to ENST00000389655 I671I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:20208963 C>T maps to ENST00000389655 I671I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:29960870 G>A maps to NM_054112.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:29960870 G>A maps to NM_054112.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:30522679 G>A maps to NM_001008409.2 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:30522679 G>A maps to NM_001008409.2 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:30730847 C>T maps to NM_014742.3 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:30730847 C>T maps to NM_014742.3 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:30785253 G>A maps to NM_002657.3 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:30785253 G>A maps to NM_002657.3 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:33568427 C>T maps to NM_020884.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:33568427 C>T maps to NM_020884.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:36012651 C>T maps to ENST00000373558 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:36012651 C>T maps to ENST00000373558 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:36641078 G>A maps to NM_014657.1 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:36641078 G>A maps to NM_014657.1 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:36855594 C>T maps to NM_001029864.1 K671K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:36855594 C>T maps to NM_001029864.1 K671K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:43572213 G>A maps to NM_006809.4 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:43572213 G>A maps to NM_006809.4 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:45354664 G>C maps to NM_030777.3 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:45354664 G>C maps to NM_030777.3 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:45874947 G>A maps to ENST00000471951 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:45874947 G>A maps to ENST00000471951 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:50407412 G>A maps to NM_020436.3 Q537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:50407412 G>A maps to NM_020436.3 Q537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:57015991 C>T maps to NM_004738.4 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:57015991 C>T maps to NM_004738.4 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:57767537 C>T maps to NM_178457.1 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:57767537 C>T maps to NM_178457.1 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:60987713 C>T maps to NM_080833.2 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:60987713 C>T maps to NM_080833.2 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:61451327 G>A maps to NM_001853.3 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:61451327 G>A maps to NM_001853.3 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:61978200 C>T maps to NM_000744.5 W591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:61978200 C>T maps to NM_000744.5 W591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:61981709 G>A maps to NM_000744.5 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:61981709 G>A maps to NM_000744.5 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:62196772 G>A maps to NM_001037335.2 F1134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr20:62196772 G>A maps to NM_001037335.2 F1134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:22841079 G>A maps to NM_004540.2 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:22841079 G>A maps to NM_004540.2 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:31768436 C>T maps to NM_181599.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:31768436 C>T maps to NM_181599.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:31869218 C>T maps to NM_181610.1 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:31869218 C>T maps to NM_181610.1 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:33954557 C>T maps to ENST00000431216 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:33954557 C>T maps to ENST00000431216 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:34921998 C>T maps to NM_138927.1 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:34921998 C>T maps to NM_138927.1 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:34957050 G>A maps to NM_017613.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:34957050 G>A maps to NM_017613.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:38538151 G>A maps to NM_003316.3 R1212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:38538151 G>A maps to NM_003316.3 R1212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:46596323 C>T maps to NM_015833.3 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:46596323 C>T maps to NM_015833.3 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:46950871 G>A maps to NM_194255.1 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr21:46950871 G>A maps to NM_194255.1 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:19865924 C>T maps to NM_006440.3 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:19865924 C>T maps to NM_006440.3 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:21799756 C>T maps to NM_015094.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:21799756 C>T maps to NM_015094.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:22277593 G>A maps to NM_014634.3 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:22277593 G>A maps to NM_014634.3 F412F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:24573697 C>T maps to NM_012295.3 F2144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:24573697 C>T maps to NM_012295.3 F2144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:29927883 G>A maps to NM_003678.4 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:29927883 G>A maps to NM_003678.4 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:30660006 G>A maps to NM_020530.3 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:30660006 G>A maps to NM_020530.3 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:38130788 G>A maps to NM_001039141.2 R1482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:38130788 G>A maps to NM_001039141.2 R1482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:38318041 C>A maps to NM_033386.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:38318041 C>A maps to NM_033386.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:40754969 C>T maps to ENST00000428371 F622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:40754969 C>T maps to ENST00000428371 F622F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:40804824 C>T maps to NM_015705.4 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:40804824 C>T maps to NM_015705.4 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:42046860 C>T maps to NM_001469.3 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:42046860 C>T maps to NM_001469.3 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:51207915 G>A maps to NM_001130923.1 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr22:51207915 G>A maps to NM_001130923.1 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:383652 C>T maps to NM_006614.2 Y189Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:383652 C>T maps to NM_006614.2 Y189Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:2777998 T>A maps to NM_175607.1 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:2777998 T>A maps to NM_175607.1 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:12198974 C>T maps to NM_003256.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:12198974 C>T maps to NM_003256.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:13407499 G>A maps to NM_024923.2 H626H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:13407499 G>A maps to NM_024923.2 H626H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:20113934 T>C maps to NM_003884.4 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:20113934 T>C maps to NM_003884.4 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:29938881 A>C maps to NM_001003793.2 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:29938881 A>C maps to NM_001003793.2 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:38087116 G>A maps to NM_007335.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:38087116 G>A maps to NM_007335.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:38743590 G>A maps to NM_006514.2 Q1466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:38743590 G>A maps to NM_006514.2 Q1466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:38748835 C>T maps to NM_006514.2 K1440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:38748835 C>T maps to NM_006514.2 K1440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:47037516 C>T maps to NM_015175.1 P709P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:47037516 C>T maps to NM_015175.1 P709P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:47378139 C>T maps to NM_025010.4 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:47378139 C>T maps to NM_025010.4 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:48677666 C>T maps to NM_001407.2 R3117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:48677666 C>T maps to NM_001407.2 R3117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:50332190 G>A maps to NM_003549.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:50332190 G>A maps to NM_003549.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:51394394 G>A maps to NM_004947.4 V1502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:51394394 G>A maps to NM_004947.4 V1502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:53157825 G>A maps to NM_052859.3 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:53157825 G>A maps to NM_052859.3 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:98188839 C>T maps to NM_001004736.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:98188839 C>T maps to NM_001004736.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:100995506 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:100995506 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:112991947 C>T maps to ENST00000273395 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:112991947 C>T maps to ENST00000273395 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:113323755 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:113323755 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:113858409 C>T maps to NM_000796.3 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:113858409 C>T maps to NM_000796.3 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:121207526 G>A maps to ENST00000393672 F1553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:121207526 G>A maps to ENST00000393672 F1553F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:125855666 C>T maps to ENST00000273450 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:125855666 C>T maps to ENST00000273450 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:129267878 G>A maps to NM_153833.1 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:129267878 G>A maps to NM_153833.1 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:130452398 G>A maps to NM_014602.2 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:130452398 G>A maps to NM_014602.2 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:136046021 C>T maps to NM_001178014.1 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:136046021 C>T maps to NM_001178014.1 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:141499322 G>A maps to NM_139209.2 K240K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:141499322 G>A maps to NM_139209.2 K240K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:142048323 G>A maps to NM_019001.3 S1451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:142048323 G>A maps to NM_019001.3 S1451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:143371182 G>A maps to NM_173653.3 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:143371182 G>A maps to NM_173653.3 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:151155337 C>T maps to NM_178822.4 P2337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:151155337 C>T maps to NM_178822.4 P2337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:165503941 C>A maps to NM_000055.2 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:165503941 C>A maps to NM_000055.2 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:179576912 G>A maps to NM_016559.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:179576912 G>A maps to NM_016559.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:183217504 C>T maps to NM_130446.2 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:183217504 C>T maps to NM_130446.2 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:183368284 C>T maps to NM_017644.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:183368284 C>T maps to NM_017644.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:184071989 C>T maps to NM_004366.4 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:184071989 C>T maps to NM_004366.4 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:190122650 C>T maps to NM_006580.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:190122650 C>T maps to NM_006580.3 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:190930353 C>T maps to NM_198184.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:190930353 C>T maps to NM_198184.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:194390863 A>G maps to NM_018385.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:194390863 A>G maps to NM_018385.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:197427592 G>A maps to NM_014687.1 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:197427592 G>A maps to NM_014687.1 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:197432013 G>A maps to NM_014687.1 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr3:197432013 G>A maps to NM_014687.1 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:25665875 G>A maps to NM_006424.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:25665875 G>A maps to NM_006424.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:40351345 G>T maps to NM_017581.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:40351345 G>T maps to NM_017581.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:44176944 C>T maps to NM_198353.2 K428K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:44176944 C>T maps to NM_198353.2 K428K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:48542475 G>A maps to NM_015030.1 F2063F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:48542475 G>A maps to NM_015030.1 F2063F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:57842905 G>A maps to NM_032313.2 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:57842905 G>A maps to NM_032313.2 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:69962534 C>T maps to NM_001074.2 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:69962534 C>T maps to NM_001074.2 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:70810587 A>G maps to NM_001890.1 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:70810587 A>G maps to NM_001890.1 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:71020139 G>A maps to NM_214711.3 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:71020139 G>A maps to NM_214711.3 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:71068543 C>T maps to NM_017855.3 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:71068543 C>T maps to NM_017855.3 F240F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:72397868 C>T maps to NM_001098484.2 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:72397868 C>T maps to NM_001098484.2 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:72425847 C>T maps to NM_001098484.2 Y992Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:72425847 C>T maps to NM_001098484.2 Y992Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:75673328 C>T maps to NM_001729.2 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:75673328 C>T maps to NM_001729.2 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:76489444 C>T maps to NM_178497.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:76489444 C>T maps to NM_178497.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:126241561 A>G maps to NM_024582.4 E1332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:126241561 A>G maps to NM_024582.4 E1332E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:129778491 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:129778491 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:175898865 C>T maps to NM_014269.4 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:175898865 C>T maps to NM_014269.4 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:177041153 C>T maps to NM_170710.4 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:177041153 C>T maps to NM_170710.4 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:177077241 C>T maps to NM_170710.4 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:177077241 C>T maps to NM_170710.4 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:183659599 G>A maps to NM_001080477.1 W1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:183659599 G>A maps to NM_001080477.1 W1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:186536270 C>T maps to ENST00000355634 R994R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr4:186536270 C>T maps to ENST00000355634 R994R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:251132 C>T maps to NM_004168.2 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:251132 C>T maps to NM_004168.2 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:13717483 C>T maps to NM_001369.2 A4215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:13717483 C>T maps to NM_001369.2 A4215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:16668424 G>A maps to NM_012334.2 I2012I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:16668424 G>A maps to NM_012334.2 I2012I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:23526912 G>A maps to NM_020227.2 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:23526912 G>A maps to NM_020227.2 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:78338146 G>A maps to NM_013391.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:78338146 G>A maps to NM_013391.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:90107096 G>A maps to NM_032119.3 Q5340Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:90107096 G>A maps to NM_032119.3 Q5340Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:94860295 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:94860295 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:121188056 G>A maps to NM_177478.1 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:121188056 G>A maps to NM_177478.1 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:128957965 A>C maps to NM_133638.3 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:128957965 A>C maps to NM_133638.3 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:134364546 G>A maps to NM_002653.4 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:134364546 G>A maps to NM_002653.4 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:137426722 C>T maps to NM_058244.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:137426722 C>T maps to NM_058244.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:137507795 G>A maps to NM_139199.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:137507795 G>A maps to NM_139199.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140187185 G>A maps to NM_018907.2 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140187185 G>A maps to NM_018907.2 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140236454 G>A maps to NM_018901.2 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140236454 G>A maps to NM_018901.2 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140249752 C>T maps to NM_018902.3 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140249752 C>T maps to NM_018902.3 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140263334 G>A maps to NM_018904.2 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140263334 G>A maps to NM_018904.2 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140475885 C>T maps to NM_018936.2 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140475885 C>T maps to NM_018936.2 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140729973 C>A maps to NM_018922.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140729973 C>A maps to NM_018922.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140740532 C>T maps to NM_018923.2 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140740532 C>T maps to NM_018923.2 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140774686 C>T maps to NM_032088.1 I769I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140774686 C>T maps to NM_032088.1 I769I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140811009 C>T maps to NM_003735.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:140811009 C>T maps to NM_003735.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:145665538 T>C maps to NM_018989.1 P1043P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:145665538 T>C maps to NM_018989.1 P1043P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:149500534 G>A maps to NM_002609.3 I834I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:149500534 G>A maps to NM_002609.3 I834I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:149514448 C>T maps to NM_002609.3 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:149514448 C>T maps to NM_002609.3 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:150892005 G>A maps to NM_001447.2 S3875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:150892005 G>A maps to NM_001447.2 S3875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:156533647 G>A maps to NM_032782.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:156533647 G>A maps to NM_032782.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:167812283 C>T maps to NM_001161661.1 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:167812283 C>T maps to NM_001161661.1 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:178359012 G>A maps to NM_030613.2 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:178359012 G>A maps to NM_030613.2 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:178413883 G>A maps to NM_000843.3 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr5:178413883 G>A maps to NM_000843.3 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:6589095 G>A maps to NM_004271.3 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:6589095 G>A maps to NM_004271.3 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:12719056 C>T maps to NM_030948.1 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:12719056 C>T maps to NM_030948.1 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:24596342 G>A maps to NM_014809.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:24596342 G>A maps to NM_014809.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:25850330 G>A maps to NM_001098486.1 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:25850330 G>A maps to NM_001098486.1 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:30627338 G>A maps to NM_003587.4 I639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:30627338 G>A maps to NM_003587.4 I639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:30862380 C>T maps to NM_013994.2 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:30862380 C>T maps to NM_013994.2 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:31324147 G>A maps to ENST00000428231 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:31324147 G>A maps to ENST00000428231 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:31829147 G>A maps to NM_000434.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:31829147 G>A maps to NM_000434.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:31919770 G>A maps to ENST00000437789 K1255K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:31919770 G>A maps to ENST00000437789 K1255K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:32024531 G>A maps to ENST00000375244 F2658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:32024531 G>A maps to ENST00000375244 F2658F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:33284360 G>A maps to NM_001145338.1 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:33284360 G>A maps to NM_001145338.1 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:33659605 G>A maps to ENST00000374316 R2453R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:33659605 G>A maps to ENST00000374316 R2453R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:33693271 C>T maps to NM_054111.4 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:33693271 C>T maps to NM_054111.4 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:35706177 G>A maps to NM_145028.3 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:35706177 G>A maps to NM_145028.3 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:36982747 C>T maps to NM_173558.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:36982747 C>T maps to NM_173558.3 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:39047474 C>T maps to NM_002062.3 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:39047474 C>T maps to NM_002062.3 F393F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:44273501 G>C maps to NM_020745.2 S441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:44273501 G>C maps to NM_020745.2 S441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:44320586 C>G maps to NM_145026.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:44320586 C>G maps to NM_145026.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:46191012 C>T maps to ENST00000405162 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:46191012 C>T maps to ENST00000405162 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:52701146 C>T maps to NM_153699.1 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:52701146 C>T maps to NM_153699.1 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:56033059 G>A maps to NM_030820.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:56033059 G>A maps to NM_030820.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:56457057 C>T maps to ENST00000361203 E4064E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:56457057 C>T maps to ENST00000361203 E4064E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:57398274 C>T maps to NM_000947.2 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:57398274 C>T maps to NM_000947.2 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:90380681 G>A maps to NM_014611.1 L4638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:90380681 G>A maps to NM_014611.1 L4638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:105198278 A>G maps to NM_020771.3 F760F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:105198278 A>G maps to NM_020771.3 F760F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:105224669 G>A maps to NM_020771.3 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:105224669 G>A maps to NM_020771.3 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:105563585 C>T maps to NM_007073.4 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:105563585 C>T maps to NM_007073.4 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:117128035 G>A maps to NM_148963.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:117128035 G>A maps to NM_148963.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:118475783 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:118475783 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:128134450 C>T maps to NM_001164685.1 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:128134450 C>T maps to NM_001164685.1 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:128411003 G>A maps to ENST00000368210 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:128411003 G>A maps to ENST00000368210 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:129634085 C>T maps to NM_000426.3 F1085F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:129634085 C>T maps to NM_000426.3 F1085F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:132029994 G>A maps to NM_001145659.1 F721F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:132029994 G>A maps to NM_001145659.1 F721F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:133014448 G>A maps to NM_004666.2 N180N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:133014448 G>A maps to NM_004666.2 N180N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:138202170 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:138202170 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:142409720 C>T maps to NM_002511.2 W25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:142409720 C>T maps to NM_002511.2 W25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:150164230 G>A maps to NM_032832.5 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:150164230 G>A maps to NM_032832.5 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:155618125 T>C maps to NM_016020.3 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:155618125 T>C maps to NM_016020.3 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:158538838 T>C maps to NM_032861.3 K441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:158538838 T>C maps to NM_032861.3 K441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:161071469 G>A maps to NM_005577.2 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:161071469 G>A maps to NM_005577.2 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:169053672 G>A maps to NM_022138.2 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr6:169053672 G>A maps to NM_022138.2 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:2559920 G>A maps to NM_001040167.1 K142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:2559920 G>A maps to NM_001040167.1 K142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:2645611 C>T maps to NM_152558.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:2645611 C>T maps to NM_152558.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:21627719 T>G maps to NM_003777.3 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:21627719 T>G maps to NM_003777.3 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:21639523 C>T maps to NM_003777.3 F929F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:21639523 C>T maps to NM_003777.3 F929F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:21744164 G>A maps to NM_003777.3 R2136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:21744164 G>A maps to NM_003777.3 R2136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:23391087 C>T maps to NM_006547.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:23391087 C>T maps to NM_006547.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:29544358 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:29544358 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:30066079 A>T maps to NM_017946.2 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:30066079 A>T maps to NM_017946.2 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:33039804 G>A maps to NM_007270.3 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:33039804 G>A maps to NM_007270.3 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:33376100 G>A maps to NM_198428.2 Q355Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:33376100 G>A maps to NM_198428.2 Q355Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:36580097 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:36580097 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:43484378 C>T maps to NM_015052.3 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:43484378 C>T maps to NM_015052.3 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:43484408 C>T maps to NM_015052.3 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:43484408 C>T maps to NM_015052.3 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:44804987 C>T maps to NM_031449.3 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:44804987 C>T maps to NM_031449.3 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:44805101 C>T maps to NM_031449.3 A722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:44805101 C>T maps to NM_031449.3 A722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:45743069 C>T maps to NM_021116.2 L850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:45743069 C>T maps to NM_021116.2 L850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:47842807 C>T maps to NM_138295.3 G2654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:47842807 C>T maps to NM_138295.3 G2654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:71488752 C>T maps to NM_031468.3 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:71488752 C>T maps to NM_031468.3 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:73604021 C>T maps to NM_022170.1 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:73604021 C>T maps to NM_022170.1 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:74193714 C>T maps to NM_000265.4 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:74193714 C>T maps to NM_000265.4 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:75687335 C>T maps to NM_005918.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:75687335 C>T maps to NM_005918.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:76019432 C>T maps to NM_080744.1 W557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:76019432 C>T maps to NM_080744.1 W557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:76019438 G>A maps to NM_080744.1 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:76019438 G>A maps to NM_080744.1 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:81381475 C>T maps to NM_000601.4 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:81381475 C>T maps to NM_000601.4 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:81381562 G>A maps to NM_000601.4 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:81381562 G>A maps to NM_000601.4 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:82545877 C>T maps to NM_033026.5 R3808R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:82545877 C>T maps to NM_033026.5 R3808R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:87459341 C>T maps to NM_138290.2 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:87459341 C>T maps to NM_138290.2 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:91632537 A>T maps to NM_005751.4 K1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:91632537 A>T maps to NM_005751.4 K1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:94034998 C>T maps to NM_000089.3 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:94034998 C>T maps to NM_000089.3 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:94919527 G>A maps to NM_001166160.1 R1346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:94919527 G>A maps to NM_001166160.1 R1346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:98501138 C>T maps to ENST00000359863 N345N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:98501138 C>T maps to ENST00000359863 N345N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:99696749 A>G maps to NM_005916.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:99696749 A>G maps to NM_005916.3 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:99998660 G>A maps to NM_017984.3 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:99998660 G>A maps to NM_017984.3 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:100033361 G>A maps to NM_145030.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:100033361 G>A maps to NM_145030.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:123302482 G>A maps to NM_207163.1 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:123302482 G>A maps to NM_207163.1 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:128446881 G>A maps to NM_022742.3 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:128446881 G>A maps to NM_022742.3 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:142574507 C>T maps to NM_018646.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:142574507 C>T maps to NM_018646.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:143053831 C>T maps to NM_001031690.2 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:143053831 C>T maps to NM_001031690.2 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:143140715 G>A maps to NM_177437.1 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:143140715 G>A maps to NM_177437.1 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:143141133 C>T maps to NM_177437.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:143141133 C>T maps to NM_177437.1 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:149477971 C>T maps to NM_198455.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:149477971 C>T maps to NM_198455.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:149494380 C>T maps to NM_198455.2 T2285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:149494380 C>T maps to NM_198455.2 T2285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:150417538 C>T maps to NM_130759.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:150417538 C>T maps to NM_130759.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:150554745 C>T maps to ENST00000416793 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:150554745 C>T maps to ENST00000416793 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:150774981 G>A maps to NM_006712.3 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:150774981 G>A maps to NM_006712.3 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:154598805 C>T maps to NM_130797.2 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:154598805 C>T maps to NM_130797.2 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:2021530 C>T maps to NM_003970.2 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:2021530 C>T maps to NM_003970.2 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:11189364 C>T maps to NM_054028.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:11189364 C>T maps to NM_054028.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:11667352 C>T maps to NM_004462.3 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:11667352 C>T maps to NM_004462.3 F125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:21925102 C>T maps to ENST00000265800 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:21925102 C>T maps to ENST00000265800 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:22262321 G>A maps to NM_001135153.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:22262321 G>A maps to NM_001135153.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:42038040 C>T maps to NM_000930.3 W351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:42038040 C>T maps to NM_000930.3 W351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:42234518 G>A maps to NM_014420.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:42234518 G>A maps to NM_014420.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:49832559 G>A maps to NM_003068.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:49832559 G>A maps to NM_003068.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:65528304 G>A maps to NM_004820.3 Q265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:65528304 G>A maps to NM_004820.3 Q265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:77766125 G>A maps to NM_024721.4 R2323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:77766125 G>A maps to NM_024721.4 R2323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:81733813 G>A maps to NM_001033723.2 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:81733813 G>A maps to NM_001033723.2 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:88885083 G>A maps to NM_152418.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:88885083 G>A maps to NM_152418.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:95262786 G>A maps to NM_181702.2 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:95262786 G>A maps to NM_181702.2 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:98155358 C>T maps to ENST00000325141 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:98155358 C>T maps to ENST00000325141 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:101174570 C>T maps to NM_003114.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:101174570 C>T maps to NM_003114.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:103310704 C>T maps to NM_015902.4 G1113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:103310704 C>T maps to NM_015902.4 G1113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:104940077 C>T maps to NM_001100117.2 S735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:104940077 C>T maps to NM_001100117.2 S735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:107782214 G>A maps to NM_139166.4 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:107782214 G>A maps to NM_139166.4 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:110131278 C>T maps to NM_003301.4 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:110131278 C>T maps to NM_003301.4 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:114326861 T>C maps to NM_198123.1 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:114326861 T>C maps to NM_198123.1 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:119945374 G>A maps to NM_002546.3 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:119945374 G>A maps to NM_002546.3 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:126011729 C>T maps to NM_003129.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:126011729 C>T maps to NM_003129.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:131792677 A>G maps to NM_001115.2 P1238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:131792677 A>G maps to NM_001115.2 P1238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:132982750 C>T maps to NM_015137.3 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:132982750 C>T maps to NM_015137.3 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:132999914 G>A maps to NM_015137.3 E677E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:132999914 G>A maps to NM_015137.3 E677E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:133899038 G>A maps to NM_003235.4 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:133899038 G>A maps to NM_003235.4 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:133984059 G>A maps to NM_003235.4 R1999R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:133984059 G>A maps to NM_003235.4 R1999R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:134147016 C>T maps to NM_003235.4 G2762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:134147016 C>T maps to NM_003235.4 G2762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:139158207 C>T maps to NM_015912.3 K1178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:139158207 C>T maps to NM_015912.3 K1178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:139164562 G>A maps to NM_015912.3 R719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:139164562 G>A maps to NM_015912.3 R719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:139890020 C>T maps to NM_152888.1 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:139890020 C>T maps to NM_152888.1 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:142500262 G>A maps to NM_207414.2 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:142500262 G>A maps to NM_207414.2 F217F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:144808903 G>A maps to NM_198488.3 P909P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:144808903 G>A maps to NM_198488.3 P909P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:144941346 G>A maps to NM_031308.1 L2025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:144941346 G>A maps to NM_031308.1 L2025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:145001817 C>T maps to NM_201380.2 V1309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr8:145001817 C>T maps to NM_201380.2 V1309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:3330438 C>T maps to NM_134428.1 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:3330438 C>T maps to NM_134428.1 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:14776176 C>T maps to ENST00000380880 R1492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:14776176 C>T maps to ENST00000380880 R1492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:15971755 C>T maps to NM_173550.2 P1301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:15971755 C>T maps to NM_173550.2 P1301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:16437493 C>T maps to NM_017637.5 W233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:16437493 C>T maps to NM_017637.5 W233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:27359211 G>A maps to NM_024761.3 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:27359211 G>A maps to NM_024761.3 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:32632799 G>A maps to NM_153809.2 S926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:32632799 G>A maps to NM_153809.2 S926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:35045472 G>A maps to NM_203299.2 R949R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:35045472 G>A maps to NM_203299.2 R949R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:35243342 C>T maps to ENST00000396787 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:35243342 C>T maps to ENST00000396787 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:37014992 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:37014992 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:37537655 G>A maps to NM_012166.2 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:37537655 G>A maps to NM_012166.2 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:38396325 G>A maps to NM_000692.3 W194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:38396325 G>A maps to NM_000692.3 W194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:73477821 A>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:73477821 A>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:79117758 G>A maps to NM_001097636.1 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:79117758 G>A maps to NM_001097636.1 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:84606512 C>T maps to NM_001001670.2 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:84606512 C>T maps to NM_001001670.2 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:85862841 A>G maps to NM_174938.4 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:85862841 A>G maps to NM_174938.4 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:90272958 C>T maps to NM_004938.2 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:90272958 C>T maps to NM_004938.2 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:93375902 C>T maps to NM_017594.3 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:93375902 C>T maps to NM_017594.3 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:95030485 G>A maps to ENST00000375660 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:95030485 G>A maps to ENST00000375660 I469I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:100672659 C>T maps to NM_016481.3 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:100672659 C>T maps to NM_016481.3 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:101340228 C>T maps to NM_005458.7 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:101340228 C>T maps to NM_005458.7 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:114090370 G>A maps to ENST00000374428 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:114090370 G>A maps to ENST00000374428 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:116224446 G>A maps to NM_144488.4 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:116224446 G>A maps to NM_144488.4 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:120476799 G>A maps to NM_138554.3 E798E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:120476799 G>A maps to NM_138554.3 E798E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:123313138 G>A maps to NM_018249.4 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:123313138 G>A maps to NM_018249.4 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:123737101 A>G maps to NM_001735.2 H1324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:123737101 A>G maps to NM_001735.2 H1324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:123880718 G>C maps to NM_007018.4 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:123880718 G>C maps to NM_007018.4 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:126132585 G>A maps to NM_173689.5 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:126132585 G>A maps to NM_173689.5 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:128321982 G>A maps to NM_001006617.1 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:128321982 G>A maps to NM_001006617.1 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:129931021 C>T maps to NM_014636.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:129931021 C>T maps to NM_014636.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:130476447 C>T maps to NM_001002913.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:130476447 C>T maps to NM_001002913.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:130581105 C>T maps to NM_001114753.1 K439K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:130581105 C>T maps to NM_001114753.1 K439K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:135698628 C>T maps to NM_152572.2 Q284Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:135698628 C>T maps to NM_152572.2 Q284Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:136029194 C>T maps to NM_021996.4 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:136029194 C>T maps to NM_021996.4 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:139944948 G>A maps to NM_203468.1 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:139944948 G>A maps to NM_203468.1 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:140078133 G>A maps to NM_013366.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:140078133 G>A maps to NM_013366.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:140323431 C>T maps to NM_006647.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:140323431 C>T maps to NM_006647.1 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:140358626 G>A maps to NM_001098537.1 F1059F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:140358626 G>A maps to NM_001098537.1 F1059F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:140389514 G>A maps to NM_001098537.1 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr9:140389514 G>A maps to NM_001098537.1 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:1742147 C>T maps to NM_001171038.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:1742147 C>T maps to NM_001171038.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:1743189 C>T maps to NM_001171038.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:1743189 C>T maps to NM_001171038.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:3239246 G>A maps to NM_015419.3 S1493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:3239246 G>A maps to NM_015419.3 S1493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:11682603 G>A maps to NM_013427.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:11682603 G>A maps to NM_013427.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:21675147 G>A maps to NM_153270.1 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:21675147 G>A maps to NM_153270.1 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:34148022 A>G maps to NM_203408.3 D791D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:34148022 A>G maps to NM_203408.3 D791D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:50147113 C>T maps to NM_001013742.1 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:50147113 C>T maps to NM_001013742.1 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:74519597 C>T maps to NM_145052.3 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:74519597 C>T maps to NM_145052.3 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:86773150 G>A maps to NM_057162.2 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:86773150 G>A maps to NM_057162.2 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:86873068 C>T maps to NM_057162.2 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:86873068 C>T maps to NM_057162.2 R288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:91132696 G>A maps to NM_032968.3 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:91132696 G>A maps to NM_032968.3 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:112021851 A>G maps to NM_001113490.1 T1066T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:112021851 A>G maps to NM_001113490.1 T1066T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:127185830 G>A maps to NM_138289.3 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:127185830 G>A maps to NM_138289.3 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:128926346 G>A maps to ENST00000443760 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:128926346 G>A maps to ENST00000443760 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:129519166 G>A maps to NM_178471.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:129519166 G>A maps to NM_178471.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:130411003 C>T maps to NM_001170961.1 V844V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:130411003 C>T maps to NM_001170961.1 V844V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:142795188 C>T maps to NM_001009615.1 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:142795188 C>T maps to NM_001009615.1 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:152807133 G>T maps to NM_001001344.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:152807133 G>T maps to NM_001001344.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:152938471 C>T maps to NM_001039582.3 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:152938471 C>T maps to NM_001039582.3 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:153208458 G>A maps to NM_002910.5 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:153208458 G>A maps to NM_002910.5 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:153539192 G>A maps to NM_012253.3 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:153539192 G>A maps to NM_012253.3 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:153589714 G>A maps to NM_001110556.1 P1056P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:153589714 G>A maps to NM_001110556.1 P1056P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:153660715 C>T maps to NM_001183.4 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:153660715 C>T maps to NM_001183.4 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrY:21869119 G>T maps to NM_001146705.1 A1335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrY:21869119 G>T maps to NM_001146705.1 A1335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr1:75072552 C>T maps to NM_001002912.4 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr1:75072552 C>T maps to NM_001002912.4 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr1:158450101 C>T maps to NM_001004472.1 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr1:158450101 C>T maps to NM_001004472.1 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr10:105201731 G>A maps to NM_014976.1 T1569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr10:105201731 G>A maps to NM_014976.1 T1569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr11:55587566 C>G maps to ENST00000395203 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr11:55587566 C>G maps to ENST00000395203 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr11:56756942 T>G maps to NM_001005323.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr11:56756942 T>G maps to NM_001005323.1 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr12:113624688 G>A maps to NM_032848.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr12:113624688 G>A maps to NM_032848.1 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr17:8047138 G>A maps to NM_002616.2 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr17:8047138 G>A maps to NM_002616.2 A839A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr18:13826448 C>A maps to NM_005913.2 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr18:13826448 C>A maps to NM_005913.2 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr19:52033053 T>G maps to NM_001245.5 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr19:52033053 T>G maps to NM_001245.5 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr20:47591349 C>T maps to NM_006420.2 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr20:47591349 C>T maps to NM_006420.2 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr3:120469671 C>G maps to NM_005513.2 Y91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr3:120469671 C>G maps to NM_005513.2 Y91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr4:88755892 C>T maps to ENST00000395102 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr4:88755892 C>T maps to ENST00000395102 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr5:43280500 G>C maps to NM_153361.2 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr5:43280500 G>C maps to NM_153361.2 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr6:27100993 G>T maps to NM_021064.4 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr6:27100993 G>T maps to NM_021064.4 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr8:30703494 T>C maps to NM_031271.3 T1013T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr8:30703494 T>C maps to NM_031271.3 T1013T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr8:107782151 A>G maps to NM_139166.4 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr8:107782151 A>G maps to NM_139166.4 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr9:32488811 C>T maps to NM_014314.3 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chr9:32488811 C>T maps to NM_014314.3 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chrX:43590579 C>T maps to NM_000240.2 H246H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chrX:43590579 C>T maps to NM_000240.2 H246H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chrX:129147296 C>A maps to ENST00000303743 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6517-01A-11D-1870-08 chrX:129147296 C>A maps to ENST00000303743 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr1:215408400 C>T maps to NM_001017425.2 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr1:215408400 C>T maps to NM_001017425.2 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr11:65826721 C>T maps to NM_006842.2 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr11:65826721 C>T maps to NM_006842.2 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr11:71939891 G>A did not map to a codon.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr11:71939891 G>A did not map to a codon.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr11:77924729 C>A maps to NM_020798.2 I976I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr11:77924729 C>A maps to NM_020798.2 I976I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr11:124756426 G>T maps to NM_019055.5 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr11:124756426 G>T maps to NM_019055.5 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr12:53201425 A>G did not map to a codon.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr12:53201425 A>G did not map to a codon.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr13:45580366 T>C maps to NM_018559.2 D84D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr13:45580366 T>C maps to NM_018559.2 D84D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr15:38773632 G>A maps to NM_173611.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr15:38773632 G>A maps to NM_173611.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr17:7497596 G>A maps to NM_004860.3 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr17:7497596 G>A maps to NM_004860.3 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr17:41256882 A>C did not map to a codon.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr17:41256882 A>C did not map to a codon.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr17:56291136 T>C maps to NM_017777.3 K246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr17:56291136 T>C maps to NM_017777.3 K246K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr18:580761 C>T maps to NM_004066.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr18:580761 C>T maps to NM_004066.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr19:16638962 G>A maps to NM_006387.5 H411H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr19:16638962 G>A maps to NM_006387.5 H411H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr19:37210258 A>G maps to ENST00000423498 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr19:37210258 A>G maps to ENST00000423498 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr19:40520757 T>C maps to NM_178544.3 C527C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr19:40520757 T>C maps to NM_178544.3 C527C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr2:219099115 A>G maps to NM_005731.2 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr2:219099115 A>G maps to NM_005731.2 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr2:234346040 G>T maps to NM_152879.2 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr2:234346040 G>T maps to NM_152879.2 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr21:43279699 C>A did not map to a codon.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr21:43279699 C>A did not map to a codon.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr22:26902302 G>A maps to NM_012143.2 Y162Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr22:26902302 G>A maps to NM_012143.2 Y162Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr3:39374724 T>G maps to NM_005201.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr3:39374724 T>G maps to NM_005201.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr3:138037034 G>A maps to ENST00000333911 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr3:138037034 G>A maps to ENST00000333911 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr5:10448389 G>A maps to NM_031916.3 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr5:10448389 G>A maps to NM_031916.3 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr6:64422439 T>A maps to NM_015153.2 P1652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr6:64422439 T>A maps to NM_015153.2 P1652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr8:125989979 C>T maps to NM_152412.2 H490H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chr8:125989979 C>T maps to NM_152412.2 H490H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chrX:29973843 G>A maps to NM_014271.3 S666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6823-01A-11D-1912-08 chrX:29973843 G>A maps to NM_014271.3 S666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr13:39358892 C>T maps to NM_207361.4 I1989I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr13:39358892 C>T maps to NM_207361.4 I1989I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr13:53217476 A>T maps to NM_001011725.1 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr13:53217476 A>T maps to NM_001011725.1 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr13:115090168 A>T maps to NM_032436.2 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr13:115090168 A>T maps to NM_032436.2 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr16:20043920 G>C maps to NM_001002911.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr16:20043920 G>C maps to NM_001002911.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr17:27958125 C>T maps to NM_033389.2 Q1335Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr17:27958125 C>T maps to NM_033389.2 Q1335Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr19:371323 T>A did not map to a codon.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr19:371323 T>A did not map to a codon.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr19:49657228 G>C maps to NM_002152.2 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr19:49657228 G>C maps to NM_002152.2 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr2:87013079 G>T maps to ENST00000456996 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr2:87013079 G>T maps to ENST00000456996 S265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr2:176043849 T>C maps to NM_001689.4 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr2:176043849 T>C maps to NM_001689.4 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr5:140476000 T>C maps to NM_018936.2 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr5:140476000 T>C maps to NM_018936.2 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr7:31862846 G>A maps to NM_001191057.1 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr7:31862846 G>A maps to NM_001191057.1 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr7:141618782 G>A maps to NM_001001656.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr7:141618782 G>A maps to NM_001001656.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr8:113662432 G>T maps to NM_198123.1 C1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr8:113662432 G>T maps to NM_198123.1 C1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr8:145154649 C>G maps to NM_030974.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr8:145154649 C>G maps to NM_030974.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr9:104448990 T>G maps to NM_133445.2 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr9:104448990 T>G maps to NM_133445.2 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chrX:101138796 A>G maps to NM_001011657.3 H534H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chrX:101138796 A>G maps to NM_001011657.3 H534H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chrX:140994644 C>T maps to NM_005462.4 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chrX:140994644 C>T maps to NM_005462.4 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr1:2451775 C>A maps to ENST00000425477 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr1:2451775 C>A maps to ENST00000425477 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr10:62647976 C>T maps to NM_014836.4 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr10:62647976 C>T maps to NM_014836.4 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr11:10064501 C>A maps to NM_030962.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr11:10064501 C>A maps to NM_030962.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr11:20139696 C>T maps to ENST00000396087 L2454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr11:20139696 C>T maps to ENST00000396087 L2454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr11:27016516 G>A maps to NM_203371.1 Q148Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr11:27016516 G>A maps to NM_203371.1 Q148Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr12:13715992 G>A maps to NM_000834.3 D1393D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr12:13715992 G>A maps to NM_000834.3 D1393D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr14:57938206 G>A maps to NM_018168.2 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr14:57938206 G>A maps to NM_018168.2 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr14:76088432 G>A maps to NM_017791.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr14:76088432 G>A maps to NM_017791.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr15:34105781 C>A did not map to a codon.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr15:34105781 C>A did not map to a codon.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr17:7578368 A>C did not map to a codon.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr17:7578368 A>C did not map to a codon.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr17:57050197 A>G maps to NM_014906.3 E374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr17:57050197 A>G maps to NM_014906.3 E374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr17:71375665 G>A maps to NM_001144952.1 Y1595Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr17:71375665 G>A maps to NM_001144952.1 Y1595Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr19:6374914 C>G maps to NM_032306.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr19:6374914 C>G maps to NM_032306.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr19:31039972 C>A maps to NM_014717.1 I1149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr19:31039972 C>A maps to NM_014717.1 I1149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr19:38897629 C>T maps to NM_174905.3 H277H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr19:38897629 C>T maps to NM_174905.3 H277H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr19:55435179 C>T maps to ENST00000446217 K1042K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr19:55435179 C>T maps to ENST00000446217 K1042K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr2:141457978 C>T maps to NM_018557.2 R2213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr2:141457978 C>T maps to NM_018557.2 R2213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr2:165551293 G>A maps to ENST00000392717 Q946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr2:165551293 G>A maps to ENST00000392717 Q946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr2:170025079 G>A maps to NM_004525.2 G3868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr2:170025079 G>A maps to NM_004525.2 G3868G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr2:208486635 G>A maps to ENST00000272839 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr2:208486635 G>A maps to ENST00000272839 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr20:21687259 C>T maps to NM_006192.3 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr20:21687259 C>T maps to NM_006192.3 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr3:30032697 T>C maps to NM_001003793.2 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr3:30032697 T>C maps to NM_001003793.2 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr3:88202408 C>T maps to NM_173824.3 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr3:88202408 C>T maps to NM_173824.3 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr3:140785629 C>T maps to NM_080862.1 N228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr3:140785629 C>T maps to NM_080862.1 N228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr3:173998385 G>T maps to NM_014932.2 G589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr3:173998385 G>T maps to NM_014932.2 G589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr4:54362402 G>A maps to NM_001126328.1 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr4:54362402 G>A maps to NM_001126328.1 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr5:140595588 G>T maps to NM_018933.2 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr5:140595588 G>T maps to NM_018933.2 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr6:97677101 G>C maps to NM_198468.2 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr6:97677101 G>C maps to NM_198468.2 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr6:148840731 C>T maps to NM_015278.3 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr6:148840731 C>T maps to NM_015278.3 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr7:100679244 A>G maps to NM_001040105.1 L1516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr7:100679244 A>G maps to NM_001040105.1 L1516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr7:121608116 A>G maps to NM_002851.2 K79K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr7:121608116 A>G maps to NM_002851.2 K79K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr7:150037212 G>C maps to NM_002889.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr7:150037212 G>C maps to NM_002889.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr9:21970999 C>A maps to NM_001195132.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6825-01A-21D-1912-08 chr9:21970999 C>A maps to NM_001195132.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr1:27690467 G>A maps to NM_004672.3 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr1:27690467 G>A maps to NM_004672.3 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr1:55148400 G>T maps to ENST00000454855 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr1:55148400 G>T maps to ENST00000454855 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr1:70502125 G>T did not map to a codon.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr1:70502125 G>T did not map to a codon.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr1:145498679 C>T maps to NM_153713.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr1:145498679 C>T maps to NM_153713.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr1:157737022 G>C maps to NM_030764.3 S387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr1:157737022 G>C maps to NM_030764.3 S387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr11:5248167 G>A maps to NM_000518.4 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr11:5248167 G>A maps to NM_000518.4 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr11:67262421 G>A maps to NM_004910.2 I879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr11:67262421 G>A maps to NM_004910.2 I879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr12:57058263 T>G maps to NM_006601.5 *161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr12:57058263 T>G maps to NM_006601.5 *161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr12:110238455 G>A maps to NM_021625.4 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr12:110238455 G>A maps to NM_021625.4 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr13:26789039 G>A maps to NM_005977.3 Q327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr13:26789039 G>A maps to NM_005977.3 Q327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr14:92588013 G>T maps to NM_004545.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr14:92588013 G>T maps to NM_004545.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr15:41120650 C>G maps to NM_001130143.1 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr15:41120650 C>G maps to NM_001130143.1 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr15:42173393 C>T maps to ENST00000320955 R832R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr15:42173393 C>T maps to ENST00000320955 R832R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr16:1642225 C>T maps to NM_014714.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr16:1642225 C>T maps to NM_014714.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr16:2287937 C>T maps to NM_001374.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr16:2287937 C>T maps to NM_001374.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr16:24372923 C>A maps to NM_006539.3 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr16:24372923 C>A maps to NM_006539.3 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr17:67178386 A>G maps to NM_080282.3 C892C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr17:67178386 A>G maps to NM_080282.3 C892C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr19:40929408 C>T maps to NM_013376.3 E15E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr19:40929408 C>T maps to NM_013376.3 E15E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr19:46190834 C>G maps to NM_004597.5 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr19:46190834 C>G maps to NM_004597.5 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr2:69302733 C>T maps to NM_032208.2 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr2:69302733 C>T maps to NM_032208.2 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr20:61637637 G>A maps to NM_080606.3 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr20:61637637 G>A maps to NM_080606.3 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr22:29708003 G>A maps to NM_152236.1 W521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr22:29708003 G>A maps to NM_152236.1 W521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr22:31059927 C>T maps to NM_152511.3 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr22:31059927 C>T maps to NM_152511.3 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr3:49947691 G>A maps to NM_032355.3 F510F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr3:49947691 G>A maps to NM_032355.3 F510F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr4:77003500 C>T maps to NM_001130016.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr4:77003500 C>T maps to NM_001130016.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr4:113352353 C>T maps to NM_025144.3 Q551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr4:113352353 C>T maps to NM_025144.3 Q551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr4:155157871 T>A maps to NM_017639.3 P2189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr4:155157871 T>A maps to NM_017639.3 P2189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr4:162307345 G>A maps to NM_020116.3 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr4:162307345 G>A maps to NM_020116.3 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr4:169215015 G>A maps to NM_017631.5 C268C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr4:169215015 G>A maps to NM_017631.5 C268C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr5:908528 C>T maps to NM_004237.3 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr5:908528 C>T maps to NM_004237.3 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr5:40798207 A>G maps to NM_206907.3 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr5:40798207 A>G maps to NM_206907.3 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr5:79028658 T>C maps to NM_153610.3 S1357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr5:79028658 T>C maps to NM_153610.3 S1357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr5:153855398 C>T maps to NM_004821.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr5:153855398 C>T maps to NM_004821.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr7:30791837 C>T maps to NM_006774.4 Y24Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr7:30791837 C>T maps to NM_006774.4 Y24Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr7:87035603 G>A maps to NM_018849.2 H1169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr7:87035603 G>A maps to NM_018849.2 H1169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr7:149489169 C>T maps to NM_198455.2 D1806D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr7:149489169 C>T maps to NM_198455.2 D1806D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chrX:2833636 G>T maps to NM_001669.2 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chrX:2833636 G>T maps to NM_001669.2 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chrX:24228853 G>A maps to NM_003410.3 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chrX:24228853 G>A maps to NM_003410.3 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chrX:47919826 A>T did not map to a codon.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chrX:47919826 A>T did not map to a codon.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chrX:148794916 T>A did not map to a codon.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chrX:148794916 T>A did not map to a codon.
Sequencing variant TCGA-D6-6827-01A-11D-1912-08 chr10:48429291 G>A maps to NM_004962.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6827-01A-11D-1912-08 chr10:48429291 G>A maps to NM_004962.2 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6827-01A-11D-1912-08 chr19:14507205 C>T maps to NM_078481.2 C133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6827-01A-11D-1912-08 chr19:14507205 C>T maps to NM_078481.2 C133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6827-01A-11D-1912-08 chr19:14877868 G>A maps to NM_013447.2 C136C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6827-01A-11D-1912-08 chr19:14877868 G>A maps to NM_013447.2 C136C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6827-01A-11D-1912-08 chr2:238275792 C>A maps to NM_004369.3 G1679G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6827-01A-11D-1912-08 chr2:238275792 C>A maps to NM_004369.3 G1679G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6827-01A-11D-1912-08 chr4:75681109 C>T maps to NM_001729.2 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6827-01A-11D-1912-08 chr4:75681109 C>T maps to NM_001729.2 G80G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DQ-5624-01A-01D-1870-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DQ-5624-01A-01D-1870-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr1:66067601 C>T maps to NM_002303.5 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr1:66067601 C>T maps to NM_002303.5 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr1:153431378 C>T maps to NM_002963.3 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr1:153431378 C>T maps to NM_002963.3 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr1:196712600 G>A maps to NM_000186.3 P1051P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr1:196712600 G>A maps to NM_000186.3 P1051P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr10:103917060 C>T maps to ENST00000405356 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr10:103917060 C>T maps to ENST00000405356 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr11:5153245 G>T maps to NM_001005160.2 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr11:5153245 G>T maps to NM_001005160.2 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr11:61551036 C>T maps to NM_001127392.1 I1028I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr11:61551036 C>T maps to NM_001127392.1 I1028I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr12:32793361 G>A maps to NM_139241.2 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr12:32793361 G>A maps to NM_139241.2 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr12:54675201 C>G maps to NM_031157.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr12:54675201 C>G maps to NM_031157.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr14:102449516 C>T maps to NM_001376.4 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr14:102449516 C>T maps to NM_001376.4 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr14:105208278 C>T maps to NM_199165.1 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr14:105208278 C>T maps to NM_199165.1 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr17:5462453 C>T maps to NM_033004.3 W521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr17:5462453 C>T maps to NM_033004.3 W521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr17:12862202 C>A maps to NM_014859.4 Y504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr17:12862202 C>A maps to NM_014859.4 Y504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr19:38951141 C>A maps to NM_000540.2 R830R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr19:38951141 C>A maps to NM_000540.2 R830R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr19:48018173 C>T maps to NM_003827.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr19:48018173 C>T maps to NM_003827.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr2:25043594 G>A maps to NM_004036.3 Q1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr2:25043594 G>A maps to NM_004036.3 Q1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr2:69565125 C>T maps to ENST00000357308 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr2:69565125 C>T maps to ENST00000357308 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr2:133489550 C>T maps to NM_207363.2 S1734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr2:133489550 C>T maps to NM_207363.2 S1734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr2:179437280 C>T maps to NM_133378.4 L21958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr2:179437280 C>T maps to NM_133378.4 L21958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr2:207615716 C>T maps to NM_001039845.1 E331E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr2:207615716 C>T maps to NM_001039845.1 E331E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr20:42935536 G>A maps to NM_001080472.1 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr20:42935536 G>A maps to NM_001080472.1 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr22:43308052 C>A maps to NM_001184970.1 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr22:43308052 C>A maps to NM_001184970.1 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr3:10088286 C>T maps to NM_033084.3 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr3:10088286 C>T maps to NM_033084.3 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr5:195215 C>T maps to NM_001080478.1 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr5:195215 C>T maps to NM_001080478.1 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr6:90440540 G>A maps to NM_014611.1 Q1682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr6:90440540 G>A maps to NM_014611.1 Q1682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr7:3991529 G>A maps to NM_152744.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr7:3991529 G>A maps to NM_152744.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr7:149575775 C>T maps to ENST00000479613 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr7:149575775 C>T maps to ENST00000479613 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr8:140631259 C>T maps to NM_016601.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr8:140631259 C>T maps to NM_016601.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr9:5923142 C>T maps to NM_001017969.2 K951K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr9:5923142 C>T maps to NM_001017969.2 K951K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr9:104239326 C>T maps to NM_032342.1 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr9:104239326 C>T maps to NM_032342.1 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr9:113171186 A>G maps to ENST00000374463 C2234C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr9:113171186 A>G maps to ENST00000374463 C2234C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chrX:54784514 C>T maps to NM_198510.2 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chrX:54784514 C>T maps to NM_198510.2 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chrX:100117562 C>T did not map to a codon.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chrX:100117562 C>T did not map to a codon.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chrX:118220566 T>C maps to NM_020721.1 Q1542Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chrX:118220566 T>C maps to NM_020721.1 Q1542Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chrX:144904512 G>A maps to NM_001144010.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chrX:144904512 G>A maps to NM_001144010.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr1:33360938 C>G maps to NM_033504.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr1:33360938 C>G maps to NM_033504.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr1:152128884 C>T maps to NM_001122965.1 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr1:152128884 C>T maps to NM_001122965.1 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr1:152187529 G>T maps to NM_001009931.1 S2192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr1:152187529 G>T maps to NM_001009931.1 S2192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr1:186084056 C>T maps to NM_031935.2 R3795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr1:186084056 C>T maps to NM_031935.2 R3795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr1:247752272 G>A maps to NM_001001915.1 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr1:247752272 G>A maps to NM_001001915.1 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr10:62648789 C>T maps to NM_014836.4 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr10:62648789 C>T maps to NM_014836.4 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr11:20483562 G>T maps to NM_005788.3 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr11:20483562 G>T maps to NM_005788.3 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr11:59828722 T>C maps to NM_006138.4 N30N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr11:59828722 T>C maps to NM_006138.4 N30N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr11:67395431 C>T maps to ENST00000376693 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr11:67395431 C>T maps to ENST00000376693 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr11:76872096 A>T maps to NM_000260.3 K427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr11:76872096 A>T maps to NM_000260.3 K427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr11:77911808 C>T maps to NM_020798.2 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr11:77911808 C>T maps to NM_020798.2 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr11:124618356 C>T maps to NM_014312.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr11:124618356 C>T maps to NM_014312.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr12:109526079 G>T maps to NM_001145375.1 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr12:109526079 G>T maps to NM_001145375.1 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr12:122825751 T>G maps to ENST00000302528 R667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr12:122825751 T>G maps to ENST00000302528 R667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr14:95596529 C>T did not map to a codon.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr14:95596529 C>T did not map to a codon.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr15:45962151 T>G maps to NM_021199.2 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr15:45962151 T>G maps to NM_021199.2 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr15:101791397 G>A maps to NM_014918.4 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr15:101791397 G>A maps to NM_014918.4 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr16:51172805 C>T maps to ENST00000251020 P1109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr16:51172805 C>T maps to ENST00000251020 P1109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr16:72821071 G>A maps to NM_006885.3 F3701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr16:72821071 G>A maps to NM_006885.3 F3701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr17:4799023 G>T maps to NM_153827.4 L1087L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr17:4799023 G>T maps to NM_153827.4 L1087L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr17:6722666 G>C maps to NM_053285.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr17:6722666 G>C maps to NM_053285.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr17:9631982 C>G maps to NM_153210.3 V1016V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr17:9631982 C>G maps to NM_153210.3 V1016V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr17:10359161 C>G maps to NM_017533.2 R675R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr17:10359161 C>G maps to NM_017533.2 R675R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr17:27903554 C>G maps to NM_001085454.1 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr17:27903554 C>G maps to NM_001085454.1 R464R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DQ-5625-01A-01D-1870-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DQ-5625-01A-01D-1870-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr19:9296834 C>G maps to NM_175883.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr19:9296834 C>G maps to NM_175883.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr19:18499465 C>T maps to NM_004864.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr19:18499465 C>T maps to NM_004864.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr19:38997013 G>T maps to NM_000540.2 L2871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr19:38997013 G>T maps to NM_000540.2 L2871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr19:39879806 C>A maps to NM_019088.2 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr19:39879806 C>A maps to NM_019088.2 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr19:52869338 A>G maps to NM_001161425.1 E236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr19:52869338 A>G maps to NM_001161425.1 E236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr19:58067716 C>T maps to NM_001039654.1 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr19:58067716 C>T maps to NM_001039654.1 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr2:32733226 C>G maps to NM_016252.3 S3294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr2:32733226 C>G maps to NM_016252.3 S3294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr2:42671136 A>G maps to NM_133329.5 Y416Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr2:42671136 A>G maps to NM_133329.5 Y416Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr2:220334042 C>T maps to NM_005876.4 I1219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr2:220334042 C>T maps to NM_005876.4 I1219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr2:220336979 G>A maps to NM_005876.4 P1289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr2:220336979 G>A maps to NM_005876.4 P1289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr21:35190746 C>G maps to NM_003024.2 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr21:35190746 C>G maps to NM_003024.2 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr22:46785345 C>T maps to NM_014246.1 L2132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr22:46785345 C>T maps to NM_014246.1 L2132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr22:50703899 G>A maps to NM_002751.5 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr22:50703899 G>A maps to NM_002751.5 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr3:12626378 C>T maps to ENST00000415519 K610K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr3:12626378 C>T maps to ENST00000415519 K610K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr3:47889746 C>T maps to NM_138615.2 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr3:47889746 C>T maps to NM_138615.2 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr3:52539120 C>A maps to NM_015136.2 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr3:52539120 C>A maps to NM_015136.2 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr3:124462849 C>T maps to NM_000373.3 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr3:124462849 C>T maps to NM_000373.3 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr3:151155069 C>A maps to NM_178822.4 E2427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr3:151155069 C>A maps to NM_178822.4 E2427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr3:195501147 G>A maps to NM_018406.5 G4324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr3:195501147 G>A maps to NM_018406.5 G4324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr4:122740556 A>T maps to NM_001237.3 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr4:122740556 A>T maps to NM_001237.3 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr4:154197119 C>T maps to NM_015271.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr4:154197119 C>T maps to NM_015271.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr6:31855969 G>C maps to ENST00000395728 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr6:31855969 G>C maps to ENST00000395728 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr6:100841663 G>A maps to ENST00000262901 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr6:100841663 G>A maps to ENST00000262901 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr6:131917141 T>C maps to ENST00000403834 V986V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr6:131917141 T>C maps to ENST00000403834 V986V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr7:138764669 G>C maps to ENST00000464606 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chr7:138764669 G>C maps to ENST00000464606 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chrX:19398255 C>T maps to NM_001001671.3 P857P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chrX:19398255 C>T maps to NM_001001671.3 P857P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chrX:30269431 G>A maps to NM_177404.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chrX:30269431 G>A maps to NM_177404.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chrX:76944322 A>T maps to NM_000489.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5625-01A-01D-1870-08 chrX:76944322 A>T maps to NM_000489.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:2160627 G>C maps to NM_003036.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:2160627 G>C maps to NM_003036.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:9775651 C>T maps to ENST00000361110 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:9775651 C>T maps to ENST00000361110 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:34667769 C>T maps to NM_001134734.1 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:34667769 C>T maps to NM_001134734.1 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:52499424 G>A maps to NM_138417.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:52499424 G>A maps to NM_138417.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:153390677 C>T maps to NM_176823.3 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:153390677 C>T maps to NM_176823.3 F40F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:158641243 C>A did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:158641243 C>A did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:158669572 G>T maps to NM_001005279.1 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:158669572 G>T maps to NM_001005279.1 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:169505919 T>C did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:169505919 T>C did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:172628385 G>C maps to NM_000639.1 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:172628385 G>C maps to NM_000639.1 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:185939516 G>T maps to NM_031935.2 G755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:185939516 G>T maps to NM_031935.2 G755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:207095235 C>A did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:207095235 C>A did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:208062191 C>G did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:208062191 C>G did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:216040364 C>A maps to ENST00000366943 V2943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:216040364 C>A maps to ENST00000366943 V2943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:230338961 C>G maps to NM_004481.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:230338961 C>G maps to NM_004481.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:237580387 A>T maps to NM_001035.2 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr1:237580387 A>T maps to NM_001035.2 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:7708843 C>A maps to ENST00000256861 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:7708843 C>A maps to ENST00000256861 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:25464375 C>T maps to NM_020752.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:25464375 C>T maps to NM_020752.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:26581416 T>C maps to NM_001134366.1 H470H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:26581416 T>C maps to NM_001134366.1 H470H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:48428898 C>T maps to NM_004962.2 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:48428898 C>T maps to NM_004962.2 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:59956301 C>T maps to NM_152230.4 Q262Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:59956301 C>T maps to NM_152230.4 Q262Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:91404849 C>T maps to NM_148977.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:91404849 C>T maps to NM_148977.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:134008361 C>T maps to NM_006426.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:134008361 C>T maps to NM_006426.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:135084730 C>T maps to NM_001109.4 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr10:135084730 C>T maps to NM_001109.4 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:1162106 G>A maps to ENST00000406844 Q566Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:1162106 G>A maps to ENST00000406844 Q566Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:2411679 C>T maps to NM_004356.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:2411679 C>T maps to NM_004356.3 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:9182328 C>T maps to NM_015213.2 E789E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:9182328 C>T maps to NM_015213.2 E789E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:26529698 A>T maps to NM_031418.2 K161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:26529698 A>T maps to NM_031418.2 K161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:55563126 G>A maps to NM_001004735.1 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:55563126 G>A maps to NM_001004735.1 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:55872955 T>G maps to NM_001005200.1 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:55872955 T>G maps to NM_001005200.1 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:62434252 G>A maps to NM_001043229.1 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:62434252 G>A maps to NM_001043229.1 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:122930364 G>C maps to NM_006597.3 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:122930364 G>C maps to NM_006597.3 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:122944442 G>C maps to NM_024769.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:122944442 G>C maps to NM_024769.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:124267067 G>A maps to NM_001005467.1 Y60Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:124267067 G>A maps to NM_001005467.1 Y60Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:125525181 G>C maps to NM_001274.4 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr11:125525181 G>C maps to NM_001274.4 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr12:9318715 T>C maps to NM_002864.2 S730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr12:9318715 T>C maps to NM_002864.2 S730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr13:38357100 C>A maps to NM_003306.1 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr13:38357100 C>A maps to NM_003306.1 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr14:20216206 G>C maps to NM_172194.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr14:20216206 G>C maps to NM_172194.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr14:34269384 C>A maps to NM_001164749.1 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr14:34269384 C>A maps to NM_001164749.1 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr14:59113677 C>T maps to NM_016651.5 S779S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr14:59113677 C>T maps to NM_016651.5 S779S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr14:70795899 C>T maps to NM_016468.5 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr14:70795899 C>T maps to NM_016468.5 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr14:88707124 C>A maps to NM_138318.2 G148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr14:88707124 C>A maps to NM_138318.2 G148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr14:105477873 T>A maps to NM_145701.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr14:105477873 T>A maps to NM_145701.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:24922762 A>G maps to NM_018958.2 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:24922762 A>G maps to NM_018958.2 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:27159965 G>T maps to NM_000810.3 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:27159965 G>T maps to NM_000810.3 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:28090151 C>G maps to NM_000275.2 G795G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:28090151 C>G maps to NM_000275.2 G795G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:48434323 G>T maps to NM_205850.2 G427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:48434323 G>T maps to NM_205850.2 G427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:49833957 C>A maps to NM_152647.2 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:49833957 C>A maps to NM_152647.2 E265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:62182497 G>A maps to NM_020821.2 A3069A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:62182497 G>A maps to NM_020821.2 A3069A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:88420303 G>A maps to NM_001012338.1 V794V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:88420303 G>A maps to NM_001012338.1 V794V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:90020343 C>T maps to NM_016321.1 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:90020343 C>T maps to NM_016321.1 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:91546341 G>T maps to NM_018668.3 Y415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr15:91546341 G>T maps to NM_018668.3 Y415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr16:11935670 C>A maps to NM_015659.2 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr16:11935670 C>A maps to NM_015659.2 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr16:16177362 C>T maps to ENST00000399408 I752I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr16:16177362 C>T maps to ENST00000399408 I752I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr16:27752187 C>G maps to NM_015202.2 S857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr16:27752187 C>G maps to NM_015202.2 S857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr16:46771855 C>T maps to NM_182493.2 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr16:46771855 C>T maps to NM_182493.2 E256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr16:55690665 T>G maps to NM_001043.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr16:55690665 T>G maps to NM_001043.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr16:70843904 C>T maps to NM_032821.2 T4887T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr16:70843904 C>T maps to NM_032821.2 T4887T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr16:75276934 G>A maps to NM_001170714.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr16:75276934 G>A maps to NM_001170714.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr17:10358337 T>C maps to NM_017533.2 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr17:10358337 T>C maps to NM_017533.2 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr17:17077274 G>A maps to NM_015134.2 E825E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr17:17077274 G>A maps to NM_015134.2 E825E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr17:26108076 G>A maps to NM_000625.4 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr17:26108076 G>A maps to NM_000625.4 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr17:47696728 G>C maps to NM_003563.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr17:47696728 G>C maps to NM_003563.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr19:1080349 T>A maps to NM_012292.2 T600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr19:1080349 T>A maps to NM_012292.2 T600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr19:9045666 G>A maps to NM_024690.2 A11988A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr19:9045666 G>A maps to NM_024690.2 A11988A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr19:16528863 C>A maps to ENST00000455140 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr19:16528863 C>A maps to ENST00000455140 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr19:37676275 A>G maps to NM_152279.3 A721A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr19:37676275 A>G maps to NM_152279.3 A721A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr19:38893837 C>T maps to NM_174905.3 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr19:38893837 C>T maps to NM_174905.3 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr2:3469390 G>C maps to NM_016030.5 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr2:3469390 G>C maps to NM_016030.5 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr2:121995389 G>A maps to NM_014553.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr2:121995389 G>A maps to NM_014553.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr2:133721319 C>T maps to NM_207363.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr2:133721319 C>T maps to NM_207363.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr2:169780146 T>C maps to NM_003742.2 G1317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr2:169780146 T>C maps to NM_003742.2 G1317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr2:179578645 G>T maps to NM_133378.4 C7669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr2:179578645 G>T maps to NM_133378.4 C7669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr2:179639114 T>C maps to NM_133378.4 P2292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr2:179639114 T>C maps to NM_133378.4 P2292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr20:9525141 C>A did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr20:9525141 C>A did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr20:60584178 T>A maps to NM_003185.3 K605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr20:60584178 T>A maps to NM_003185.3 K605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr20:62837125 G>T maps to NM_004535.2 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr20:62837125 G>T maps to NM_004535.2 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr22:26040616 G>A maps to NM_005160.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr22:26040616 G>A maps to NM_005160.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:37034471 C>A maps to NM_014805.3 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:37034471 C>A maps to NM_014805.3 E33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:97596760 G>T maps to ENST00000182096 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:97596760 G>T maps to ENST00000182096 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:101390838 T>A maps to NM_014415.3 K177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:101390838 T>A maps to NM_014415.3 K177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:108335437 G>A maps to NM_014648.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:108335437 G>A maps to NM_014648.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:121260260 G>T maps to ENST00000393672 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:121260260 G>T maps to ENST00000393672 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:122629073 C>A maps to NM_001031702.2 T1124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:122629073 C>A maps to NM_001031702.2 T1124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:128202702 C>T maps to NM_032638.4 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:128202702 C>T maps to NM_032638.4 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:130405133 C>T maps to NM_014602.2 A1132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:130405133 C>T maps to NM_014602.2 A1132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:138738792 C>A maps to NM_001013650.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:138738792 C>A maps to NM_001013650.2 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:170819287 C>T maps to NM_015028.2 E847E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:170819287 C>T maps to NM_015028.2 E847E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:179103448 A>T maps to NM_033540.2 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:179103448 A>T maps to NM_033540.2 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:182841989 G>T maps to NM_014398.3 S377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr3:182841989 G>T maps to NM_014398.3 S377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr4:48152890 G>C maps to NM_003215.2 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr4:48152890 G>C maps to NM_003215.2 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr4:52861264 G>A maps to NM_001024611.1 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr4:52861264 G>A maps to NM_001024611.1 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr4:69519768 G>T maps to NM_001076.2 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr4:69519768 G>T maps to NM_001076.2 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr4:71232542 C>A maps to NM_012390.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr4:71232542 C>A maps to NM_012390.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr4:155253698 C>A maps to NM_017639.3 G722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr4:155253698 C>A maps to NM_017639.3 G722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr4:156717622 T>A maps to ENST00000502959 L335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr4:156717622 T>A maps to ENST00000502959 L335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:13900482 C>T maps to NM_001369.2 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:13900482 C>T maps to NM_001369.2 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:102343266 G>T maps to NM_000919.3 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:102343266 G>T maps to NM_000919.3 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:140712200 C>A maps to NM_018912.2 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:140712200 C>A maps to NM_018912.2 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:140751805 G>T maps to NM_018924.2 G615G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:140751805 G>T maps to NM_018924.2 G615G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:140755542 C>G maps to NM_018919.2 A631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:140755542 C>G maps to NM_018919.2 A631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:140764013 G>C maps to NM_018920.2 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:140764013 G>C maps to NM_018920.2 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:168671712 G>T maps to NM_003062.2 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:168671712 G>T maps to NM_003062.2 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:176396023 G>A maps to ENST00000377219 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr5:176396023 G>A maps to ENST00000377219 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:25851035 C>T maps to NM_001098486.1 W261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:25851035 C>T maps to NM_001098486.1 W261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:26108147 T>A maps to NM_005323.3 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:26108147 T>A maps to NM_005323.3 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:27101035 G>A maps to NM_021064.4 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:27101035 G>A maps to NM_021064.4 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:33145003 T>A did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:33145003 T>A did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:54025220 A>T maps to ENST00000502396 P782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:54025220 A>T maps to ENST00000502396 P782P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:56357098 G>A maps to ENST00000361203 R6684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:56357098 G>A maps to ENST00000361203 R6684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:75806968 C>T maps to ENST00000322507 P2859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:75806968 C>T maps to ENST00000322507 P2859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:99850545 C>T maps to NM_032870.2 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:99850545 C>T maps to NM_032870.2 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:118887219 G>C maps to NM_001042475.2 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:118887219 G>C maps to NM_001042475.2 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:166578114 G>A maps to NM_003181.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr6:166578114 G>A maps to NM_003181.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr7:20371491 A>T maps to NM_002214.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr7:20371491 A>T maps to NM_002214.2 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr7:48443310 C>T maps to NM_152701.3 Q3969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr7:48443310 C>T maps to NM_152701.3 Q3969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr7:81579767 G>T maps to NM_000722.2 I1072I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr7:81579767 G>T maps to NM_000722.2 I1072I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr7:95664995 G>A maps to NM_004411.4 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr7:95664995 G>A maps to NM_004411.4 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr7:147869370 C>A maps to NM_014141.5 I937I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr7:147869370 C>A maps to NM_014141.5 I937I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr7:151133381 G>A maps to NM_144727.1 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr7:151133381 G>A maps to NM_144727.1 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr8:21960043 C>T maps to NM_022749.5 I666I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr8:21960043 C>T maps to NM_022749.5 I666I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr8:77766926 C>T maps to NM_024721.4 C2590C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr8:77766926 C>T maps to NM_024721.4 C2590C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr9:21970899 C>A did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr9:21970899 C>A did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr9:125673994 G>A maps to NM_006626.4 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr9:125673994 G>A maps to NM_006626.4 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr9:132565577 C>T maps to NM_014506.1 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr9:132565577 C>T maps to NM_014506.1 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr9:135205409 G>A maps to ENST00000372169 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr9:135205409 G>A maps to ENST00000372169 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chrX:35969931 C>T maps to NM_152632.3 Q300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chrX:35969931 C>T maps to NM_152632.3 Q300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chrX:54784524 G>C maps to NM_198510.2 S661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chrX:54784524 G>C maps to NM_198510.2 S661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chrX:155003584 C>T maps to NM_005840.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chrX:155003584 C>T maps to NM_005840.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr1:12446278 C>T maps to NM_015378.2 S3840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr1:12446278 C>T maps to NM_015378.2 S3840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr1:55118865 C>A maps to ENST00000454855 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr1:55118865 C>A maps to ENST00000454855 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr1:91851391 C>G did not map to a codon.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr1:91851391 C>G did not map to a codon.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr1:156770248 C>T maps to NM_005973.4 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr1:156770248 C>T maps to NM_005973.4 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr1:176993767 A>T maps to ENST00000281881 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr1:176993767 A>T maps to ENST00000281881 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr10:115980378 G>A maps to NM_198795.1 Q849Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr10:115980378 G>A maps to NM_198795.1 Q849Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr11:93778849 T>G maps to NM_001098672.1 L61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr11:93778849 T>G maps to NM_001098672.1 L61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr14:36004165 C>T maps to NM_032594.3 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr14:36004165 C>T maps to NM_032594.3 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr14:90730031 G>C maps to NM_002802.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr14:90730031 G>C maps to NM_002802.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr15:37184421 A>G maps to NM_170675.2 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr15:37184421 A>G maps to NM_170675.2 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr19:7914194 C>T maps to NM_001159944.1 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr19:7914194 C>T maps to NM_001159944.1 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr19:36353393 G>T did not map to a codon.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr19:36353393 G>T did not map to a codon.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr2:85051177 C>T maps to ENST00000409520 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr2:85051177 C>T maps to ENST00000409520 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr2:102642599 C>T maps to NM_004633.3 Y305Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr2:102642599 C>T maps to NM_004633.3 Y305Y. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DQ-5630-01A-01D-1870-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DQ-5630-01A-01D-1870-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr3:119534275 C>G maps to NM_022002.2 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr3:119534275 C>G maps to NM_022002.2 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr3:157820661 C>G maps to NM_003030.4 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr3:157820661 C>G maps to NM_003030.4 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr3:195517409 A>G maps to NM_018406.5 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr3:195517409 A>G maps to NM_018406.5 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr4:4864701 G>A maps to NM_002448.3 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr4:4864701 G>A maps to NM_002448.3 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr4:123797545 G>A maps to NM_002006.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr4:123797545 G>A maps to NM_002006.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr4:187004156 C>T maps to NM_003265.2 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr4:187004156 C>T maps to NM_003265.2 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr5:177163582 C>A maps to ENST00000425383 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr5:177163582 C>A maps to ENST00000425383 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr6:26027282 C>T maps to NM_003544.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr6:26027282 C>T maps to NM_003544.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr6:90578309 A>T maps to NM_012115.3 I1767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr6:90578309 A>T maps to NM_012115.3 I1767I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr6:131206331 A>G maps to NM_001431.3 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr6:131206331 A>G maps to NM_001431.3 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr6:160199707 G>A maps to NM_005891.2 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr6:160199707 G>A maps to NM_005891.2 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr7:31378674 C>A maps to NM_022728.2 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr7:31378674 C>A maps to NM_022728.2 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr7:87229507 T>C did not map to a codon.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr7:87229507 T>C did not map to a codon.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr7:111368415 G>A maps to ENST00000428084 R1948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr7:111368415 G>A maps to ENST00000428084 R1948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr8:102589742 C>T maps to NM_024915.3 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr8:102589742 C>T maps to NM_024915.3 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr9:21187443 G>A maps to NM_021068.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5630-01A-01D-1870-08 chr9:21187443 G>A maps to NM_021068.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr1:7724490 G>A maps to NM_015215.2 E628E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr1:7724490 G>A maps to NM_015215.2 E628E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr1:103444278 G>A maps to NM_080629.2 G925G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr1:103444278 G>A maps to NM_080629.2 G925G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr1:161596178 G>C maps to ENST00000367964 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr1:161596178 G>C maps to ENST00000367964 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr10:1046660 G>A maps to NM_012341.2 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr10:1046660 G>A maps to NM_012341.2 R233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr10:22048518 C>T maps to NM_022365.3 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr10:22048518 C>T maps to NM_022365.3 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr10:64416232 C>T maps to NM_199451.2 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr10:64416232 C>T maps to NM_199451.2 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr10:102045959 G>C maps to NM_173809.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr10:102045959 G>C maps to NM_173809.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr11:803326 G>A maps to NM_145886.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr11:803326 G>A maps to NM_145886.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr11:77378519 C>T maps to NM_016578.3 K1256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr11:77378519 C>T maps to NM_016578.3 K1256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr11:92600370 G>A maps to ENST00000298047 S4041S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr11:92600370 G>A maps to ENST00000298047 S4041S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr11:93803696 C>T maps to NM_001098672.1 N407N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr11:93803696 C>T maps to NM_001098672.1 N407N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr12:56494867 T>C maps to NM_001982.2 S1075S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr12:56494867 T>C maps to NM_001982.2 S1075S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr14:50626719 G>A maps to NM_006939.2 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr14:50626719 G>A maps to NM_006939.2 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr14:96851942 C>G maps to NM_016472.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr14:96851942 C>G maps to NM_016472.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr16:19553368 C>G maps to NM_014711.4 S737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr16:19553368 C>G maps to NM_014711.4 S737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr17:7574020 C>A maps to NM_001126112.1 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr17:7574020 C>A maps to NM_001126112.1 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr17:10364305 G>A maps to NM_017533.2 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr17:10364305 G>A maps to NM_017533.2 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr17:18659467 G>A did not map to a codon.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr17:18659467 G>A did not map to a codon.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr17:48685318 G>A maps to NM_018896.3 E1548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr17:48685318 G>A maps to NM_018896.3 E1548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr17:73748587 C>T maps to NM_001005619.1 F1346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr17:73748587 C>T maps to NM_001005619.1 F1346F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr19:9060889 A>G maps to NM_024690.2 P8852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr19:9060889 A>G maps to NM_024690.2 P8852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr19:33647372 C>T maps to NM_173479.3 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr19:33647372 C>T maps to NM_173479.3 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr19:53959368 C>T maps to NM_001008401.3 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr19:53959368 C>T maps to NM_001008401.3 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr19:55450944 C>T maps to ENST00000446217 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr19:55450944 C>T maps to ENST00000446217 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr2:182423401 G>A maps to NM_001030311.2 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr2:182423401 G>A maps to NM_001030311.2 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr2:183616458 C>T maps to NM_018981.1 Q461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr2:183616458 C>T maps to NM_018981.1 Q461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr2:237374155 G>A maps to ENST00000457693 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr2:237374155 G>A maps to ENST00000457693 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr21:28338152 G>A maps to NM_007038.3 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr21:28338152 G>A maps to NM_007038.3 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr3:48921542 T>C maps to NM_000387.4 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr3:48921542 T>C maps to NM_000387.4 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr4:40440733 C>T maps to NM_001098634.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr4:40440733 C>T maps to NM_001098634.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr4:187542860 G>A maps to ENST00000260147 R1630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr4:187542860 G>A maps to ENST00000260147 R1630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr6:27100328 C>T maps to NM_021058.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr6:27100328 C>T maps to NM_021058.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr7:73117213 G>A maps to NM_004603.3 H213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr7:73117213 G>A maps to NM_004603.3 H213H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr7:100684620 C>A maps to NM_001040105.1 T3308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr7:100684620 C>A maps to NM_001040105.1 T3308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr7:150878271 G>A maps to ENST00000422024 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr7:150878271 G>A maps to ENST00000422024 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr8:142146791 G>A maps to NM_014957.2 W16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr8:142146791 G>A maps to NM_014957.2 W16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr8:144893097 G>A maps to NM_182706.3 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr8:144893097 G>A maps to NM_182706.3 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chrX:2998963 C>T maps to NM_004042.3 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chrX:2998963 C>T maps to NM_004042.3 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chrX:3573308 G>A maps to NM_005044.4 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chrX:3573308 G>A maps to NM_005044.4 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chrX:16635318 T>C maps to NM_001144002.1 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chrX:16635318 T>C maps to NM_001144002.1 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chrX:20082894 C>T maps to NM_001168465.1 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chrX:20082894 C>T maps to NM_001168465.1 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr1:23235658 C>T maps to ENST00000400191 Q833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr1:23235658 C>T maps to ENST00000400191 Q833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr1:50642773 G>T maps to NM_021952.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr1:50642773 G>T maps to NM_021952.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr1:149880766 A>T maps to NM_014849.3 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr1:149880766 A>T maps to NM_014849.3 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr1:198713185 C>T maps to ENST00000271610 Q901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr1:198713185 C>T maps to ENST00000271610 Q901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr1:214585061 G>A maps to NM_005401.4 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr1:214585061 G>A maps to NM_005401.4 Q159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr1:248059404 G>T maps to NM_001001957.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr1:248059404 G>T maps to NM_001001957.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr10:24762686 G>A maps to NM_019590.3 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr10:24762686 G>A maps to NM_019590.3 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr11:11913621 C>G maps to ENST00000399455 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr11:11913621 C>G maps to ENST00000399455 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr11:60702151 C>T maps to NM_017870.3 H585H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr11:60702151 C>T maps to NM_017870.3 H585H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr11:93483548 C>A maps to ENST00000354421 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr11:93483548 C>A maps to ENST00000354421 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr12:11174443 G>A maps to NM_176888.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr12:11174443 G>A maps to NM_176888.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr12:19501414 C>A maps to ENST00000429027 S989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr12:19501414 C>A maps to ENST00000429027 S989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr12:81331432 G>C maps to NM_004664.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr12:81331432 G>C maps to NM_004664.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr12:116444183 A>G maps to NM_015335.4 T757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr12:116444183 A>G maps to NM_015335.4 T757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr14:20852262 C>T maps to NM_007110.4 L1156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr14:20852262 C>T maps to NM_007110.4 L1156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr14:23444270 G>A maps to NM_032876.4 R428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr14:23444270 G>A maps to NM_032876.4 R428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr15:96875681 C>A maps to NM_021005.3 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr15:96875681 C>A maps to NM_021005.3 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr16:28992918 G>A maps to NM_032038.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr16:28992918 G>A maps to NM_032038.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr16:30780712 G>A maps to NM_014771.2 K818K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr16:30780712 G>A maps to NM_014771.2 K818K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr16:56878496 G>A maps to NM_014669.3 V812V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr16:56878496 G>A maps to NM_014669.3 V812V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr16:74499651 T>C maps to NM_012201.5 V863V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr16:74499651 T>C maps to NM_012201.5 V863V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr17:1028565 G>A maps to NM_021962.2 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr17:1028565 G>A maps to NM_021962.2 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr18:51851188 A>T maps to NM_139171.1 L179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr18:51851188 A>T maps to NM_139171.1 L179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr19:11470231 C>T maps to NM_022737.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr19:11470231 C>T maps to NM_022737.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr19:19790751 C>G maps to NM_033204.2 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr19:19790751 C>G maps to NM_033204.2 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr19:21477104 C>T maps to NM_021269.2 E221E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr19:21477104 C>T maps to NM_021269.2 E221E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr19:49379061 C>G maps to NM_014330.3 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr19:49379061 C>G maps to NM_014330.3 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr19:53644811 G>A maps to NM_001172674.1 H424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr19:53644811 G>A maps to NM_001172674.1 H424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr19:54802684 G>A maps to ENST00000251375 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr19:54802684 G>A maps to ENST00000251375 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr2:27662653 C>T maps to ENST00000379863 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr2:27662653 C>T maps to ENST00000379863 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr2:44104781 T>A maps to NM_022437.2 Y613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr2:44104781 T>A maps to NM_022437.2 Y613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr2:73518917 G>A maps to NM_001965.3 H479H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr2:73518917 G>A maps to NM_001965.3 H479H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr21:34889434 G>A maps to NM_001136006.1 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr21:34889434 G>A maps to NM_001136006.1 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr22:18022013 C>T maps to ENST00000400579 Q707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr22:18022013 C>T maps to ENST00000400579 Q707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr22:29627088 C>A maps to NM_133455.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr22:29627088 C>A maps to NM_133455.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr22:32889110 A>G maps to NM_012179.3 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr22:32889110 A>G maps to NM_012179.3 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr3:124103784 C>T maps to NM_001024660.3 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr3:124103784 C>T maps to NM_001024660.3 R620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr5:40765030 G>A maps to NM_206907.3 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr5:40765030 G>A maps to NM_206907.3 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr5:40765108 G>A maps to NM_206907.3 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr5:40765108 G>A maps to NM_206907.3 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr6:55223757 C>A maps to NM_207410.2 C258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr6:55223757 C>A maps to NM_207410.2 C258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr7:37955806 G>A maps to ENST00000223214 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr7:37955806 G>A maps to ENST00000223214 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr8:11412839 G>C did not map to a codon.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr8:11412839 G>C did not map to a codon.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr9:2101567 A>G did not map to a codon.
Sequencing variant TCGA-DQ-7588-01A-11D-2078-08 chr9:2101567 A>G did not map to a codon.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:16774624 G>A maps to NM_018090.4 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:16774624 G>A maps to NM_018090.4 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:22921774 G>A maps to NM_020526.3 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:22921774 G>A maps to NM_020526.3 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:85036298 G>T maps to NM_004388.2 Y94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:85036298 G>T maps to NM_004388.2 Y94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:102290582 T>A maps to ENST00000338858 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:102290582 T>A maps to ENST00000338858 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:149859286 G>T maps to NM_175065.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:149859286 G>T maps to NM_175065.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:149906926 C>A maps to NM_001145862.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:149906926 C>A maps to NM_001145862.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:153660622 G>A maps to NM_000906.3 Q781Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:153660622 G>A maps to NM_000906.3 Q781Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:203192646 C>T maps to NM_003465.2 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:203192646 C>T maps to NM_003465.2 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:240979622 T>C maps to ENST00000407727 Q259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:240979622 T>C maps to ENST00000407727 Q259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:247752083 C>T maps to NM_001001915.1 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr1:247752083 C>T maps to NM_001001915.1 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr11:55606466 T>A maps to NM_001005496.1 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr11:55606466 T>A maps to NM_001005496.1 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr11:89885503 C>T maps to NM_005467.3 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr11:89885503 C>T maps to NM_005467.3 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr11:102991187 A>T maps to NM_001080463.1 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr11:102991187 A>T maps to NM_001080463.1 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr12:4919518 C>A maps to NM_002235.3 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr12:4919518 C>A maps to NM_002235.3 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr12:25297595 T>C maps to NM_018272.3 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr12:25297595 T>C maps to NM_018272.3 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr12:75444617 C>T maps to NM_139137.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr12:75444617 C>T maps to NM_139137.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr12:81503350 A>G maps to NM_024560.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr12:81503350 A>G maps to NM_024560.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr12:130851758 A>G maps to NM_004764.4 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr12:130851758 A>G maps to NM_004764.4 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr13:26125579 G>T maps to NM_016529.4 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr13:26125579 G>T maps to NM_016529.4 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr13:99483676 G>C maps to ENST00000428223 S1497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr13:99483676 G>C maps to ENST00000428223 S1497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr14:47426703 C>T maps to NM_001113498.2 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr14:47426703 C>T maps to NM_001113498.2 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr14:105618507 G>C maps to NM_002226.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr14:105618507 G>C maps to NM_002226.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr15:31794040 C>G maps to ENST00000382902 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr15:31794040 C>G maps to ENST00000382902 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr15:63855162 A>G maps to NM_006537.2 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr15:63855162 A>G maps to NM_006537.2 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr17:34304697 C>T maps to NM_004590.2 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr17:34304697 C>T maps to NM_004590.2 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr18:5416371 A>T maps to NM_012307.2 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr18:5416371 A>T maps to NM_012307.2 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr18:33706694 T>A maps to NM_012319.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr18:33706694 T>A maps to NM_012319.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr19:11327706 C>T maps to ENST00000319867 W1259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr19:11327706 C>T maps to ENST00000319867 W1259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr19:16630504 A>T maps to NM_006387.5 S828S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr19:16630504 A>T maps to NM_006387.5 S828S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr19:21713484 A>T maps to NM_001001415.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr19:21713484 A>T maps to NM_001001415.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr19:31769771 G>T maps to NM_020856.2 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr19:31769771 G>T maps to NM_020856.2 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr19:51729134 G>T maps to NM_001772.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr19:51729134 G>T maps to NM_001772.3 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr2:71747931 C>A maps to NM_001130987.1 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr2:71747931 C>A maps to NM_001130987.1 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr2:108924877 A>G maps to ENST00000437390 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr2:108924877 A>G maps to ENST00000437390 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr2:189873732 T>G maps to NM_000090.3 A1203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr2:189873732 T>G maps to NM_000090.3 A1203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr20:25477375 C>T maps to NM_025176.4 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr20:25477375 C>T maps to NM_025176.4 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr21:15872960 C>G maps to ENST00000285670 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr21:15872960 C>G maps to ENST00000285670 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr3:23932087 C>A maps to NM_003341.3 Y191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr3:23932087 C>A maps to NM_003341.3 Y191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr3:48453894 C>T maps to NM_001130082.1 L1663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr3:48453894 C>T maps to NM_001130082.1 L1663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr3:124456710 G>T maps to NM_000373.3 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr3:124456710 G>T maps to NM_000373.3 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr3:140285007 G>A maps to NM_022131.2 E927E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr3:140285007 G>A maps to NM_022131.2 E927E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr3:164764694 A>T maps to NM_001041.3 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr3:164764694 A>T maps to NM_001041.3 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr4:74364894 G>T maps to NM_001133.2 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr4:74364894 G>T maps to NM_001133.2 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr4:165118635 C>A maps to NM_012403.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr4:165118635 C>A maps to NM_012403.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr6:107955646 A>T maps to NM_018013.3 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr6:107955646 A>T maps to NM_018013.3 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr6:145142115 G>A maps to NM_007124.2 L3152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr6:145142115 G>A maps to NM_007124.2 L3152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr6:158359774 G>A maps to NM_016224.3 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr6:158359774 G>A maps to NM_016224.3 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr7:70800593 T>C maps to NM_022479.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr7:70800593 T>C maps to NM_022479.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr7:89887456 C>T maps to NM_001039706.2 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr7:89887456 C>T maps to NM_001039706.2 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr7:100459151 G>T maps to NM_020246.2 A494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr7:100459151 G>T maps to NM_020246.2 A494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr7:123302929 T>C maps to NM_207163.1 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr7:123302929 T>C maps to NM_207163.1 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr8:62475422 G>A maps to NM_004318.3 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr8:62475422 G>A maps to NM_004318.3 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr8:73849809 C>T maps to NM_004770.2 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr8:73849809 C>T maps to NM_004770.2 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr8:114111058 G>C maps to NM_198123.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr8:114111058 G>C maps to NM_198123.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr9:37356933 G>A maps to NM_032226.2 W434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr9:37356933 G>A maps to NM_032226.2 W434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr9:137806601 C>A maps to NM_002003.3 G91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chr9:137806601 C>A maps to NM_002003.3 G91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chrX:48337082 G>T maps to NM_012280.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chrX:48337082 G>T maps to NM_012280.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chrX:69945164 A>C maps to NM_001003811.1 L306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7589-01A-11D-2229-08 chrX:69945164 A>C maps to NM_001003811.1 L306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr1:23519917 C>T maps to NM_000864.4 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr1:23519917 C>T maps to NM_000864.4 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr1:33149860 A>G maps to NM_030786.2 Y452Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr1:33149860 A>G maps to NM_030786.2 Y452Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr16:57007304 G>A maps to NM_000078.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr16:57007304 G>A maps to NM_000078.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr22:50854549 G>A maps to ENST00000216061 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr22:50854549 G>A maps to ENST00000216061 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr7:1588284 G>A maps to NM_001097620.1 N228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr7:1588284 G>A maps to NM_001097620.1 N228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr8:28017756 A>T maps to NM_018091.5 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr8:28017756 A>T maps to NM_018091.5 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr8:110099807 G>T maps to NM_003301.4 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7590-01A-11D-2229-08 chr8:110099807 G>T maps to NM_003301.4 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr10:78708932 C>T maps to NM_001161352.1 T892T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr10:78708932 C>T maps to NM_001161352.1 T892T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr10:97607264 C>T maps to NM_001098175.1 N299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr10:97607264 C>T maps to NM_001098175.1 N299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr11:31616336 T>A maps to ENST00000395934 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr11:31616336 T>A maps to ENST00000395934 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr15:28375740 C>T did not map to a codon.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr15:28375740 C>T did not map to a codon.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr15:57913835 C>T maps to NM_001018090.3 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr15:57913835 C>T maps to NM_001018090.3 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr16:65032648 G>A maps to NM_001797.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr16:65032648 G>A maps to NM_001797.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr17:10448711 C>T maps to NM_017534.5 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr17:10448711 C>T maps to NM_017534.5 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr2:210594940 T>A maps to NM_002374.3 A1768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr2:210594940 T>A maps to NM_002374.3 A1768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr2:228009237 T>A maps to ENST00000396625 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr2:228009237 T>A maps to ENST00000396625 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr5:98233987 G>T maps to NM_001270.2 S446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr5:98233987 G>T maps to NM_001270.2 S446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr8:42196203 G>T did not map to a codon.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr8:42196203 G>T did not map to a codon.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr8:145139220 G>A maps to NM_003801.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr8:145139220 G>A maps to NM_003801.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr8:145655882 G>A maps to NM_013432.4 L1283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr8:145655882 G>A maps to NM_013432.4 L1283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr9:90501078 C>T maps to NM_178828.4 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7591-01A-11D-2078-08 chr9:90501078 C>T maps to NM_178828.4 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr1:22413013 A>G maps to NM_001039802.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr1:22413013 A>G maps to NM_001039802.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr1:52810540 C>G maps to NM_004799.2 L1347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr1:52810540 C>G maps to NM_004799.2 L1347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr1:216258089 C>T maps to ENST00000366943 W1706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr1:216258089 C>T maps to ENST00000366943 W1706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr1:248790243 C>T maps to NM_001001964.1 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr1:248790243 C>T maps to NM_001001964.1 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr11:6008145 A>G maps to NM_001005173.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr11:6008145 A>G maps to NM_001005173.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr11:7670884 G>A maps to NM_003621.2 E707E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr11:7670884 G>A maps to NM_003621.2 E707E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr11:68846463 C>T maps to NM_139075.3 D505D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr11:68846463 C>T maps to NM_139075.3 D505D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr12:9334672 G>A maps to NM_002864.2 D529D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr12:9334672 G>A maps to NM_002864.2 D529D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr12:15636951 C>T maps to NM_030667.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr12:15636951 C>T maps to NM_030667.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr12:60169146 T>G maps to NM_004731.3 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr12:60169146 T>G maps to NM_004731.3 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr13:28589747 G>A maps to NM_004119.2 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr13:28589747 G>A maps to NM_004119.2 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr13:53421569 G>A maps to NM_002590.2 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr13:53421569 G>A maps to NM_002590.2 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr15:31776456 C>T maps to ENST00000382902 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr15:31776456 C>T maps to ENST00000382902 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr16:67267887 G>T maps to NM_013241.2 S573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr16:67267887 G>T maps to NM_013241.2 S573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr19:46915758 G>A maps to NM_032040.3 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr19:46915758 G>A maps to NM_032040.3 S103S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DQ-7592-01A-11D-2078-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr19:46998416 G>A maps to ENST00000377652 R176R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DQ-7592-01A-11D-2078-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr19:46998416 G>A maps to ENST00000377652 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr19:58131570 G>A maps to NM_003435.3 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr19:58131570 G>A maps to NM_003435.3 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr20:57769697 G>A maps to NM_178457.1 A1208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr20:57769697 G>A maps to NM_178457.1 A1208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr3:120053937 A>C maps to NM_001099678.1 Y226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr3:120053937 A>C maps to NM_001099678.1 Y226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr3:120495327 G>T maps to NM_005513.2 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr3:120495327 G>T maps to NM_005513.2 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr3:128181533 G>A maps to NM_153330.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr3:128181533 G>A maps to NM_153330.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr4:3424167 C>T maps to NM_198229.2 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr4:3424167 C>T maps to NM_198229.2 L968L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr4:70460412 T>C maps to ENST00000514019 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr4:70460412 T>C maps to ENST00000514019 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr5:10280583 C>T maps to NM_138809.3 W240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr5:10280583 C>T maps to NM_138809.3 W240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr5:156381756 A>C maps to NM_138379.2 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr5:156381756 A>C maps to NM_138379.2 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr6:27806705 C>T maps to NM_003520.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr6:27806705 C>T maps to NM_003520.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr6:99353452 G>A maps to NM_012160.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr6:99353452 G>A maps to NM_012160.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr7:4874237 C>T maps to NM_018059.4 W472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr7:4874237 C>T maps to NM_018059.4 W472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr7:23306161 C>T maps to ENST00000435486 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr7:23306161 C>T maps to ENST00000435486 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr8:88885017 G>A maps to NM_152418.3 Y394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr8:88885017 G>A maps to NM_152418.3 Y394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr9:73152299 C>T maps to ENST00000419692 R1197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr9:73152299 C>T maps to ENST00000419692 R1197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr9:112705029 T>C maps to ENST00000413420 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr9:112705029 T>C maps to ENST00000413420 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr9:131843486 G>C did not map to a codon.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr9:131843486 G>C did not map to a codon.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chrX:79698532 C>T maps to NM_001170574.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chrX:79698532 C>T maps to NM_001170574.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr11:66456267 G>A maps to NM_006946.2 L2029L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr11:66456267 G>A maps to NM_006946.2 L2029L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr12:52818393 G>A maps to ENST00000252245 F575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr12:52818393 G>A maps to ENST00000252245 F575F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr13:46619637 G>C maps to ENST00000242848 S2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr13:46619637 G>C maps to ENST00000242848 S2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr13:48947539 G>A did not map to a codon.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr13:48947539 G>A did not map to a codon.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr14:59113461 G>A maps to NM_016651.5 A707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr14:59113461 G>A maps to NM_016651.5 A707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr14:62547862 C>T maps to NM_031914.2 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr14:62547862 C>T maps to NM_031914.2 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr14:101200716 C>T maps to NM_003836.5 C212C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr14:101200716 C>T maps to NM_003836.5 C212C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr15:44166083 C>T maps to NM_032892.3 *571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr15:44166083 C>T maps to NM_032892.3 *571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr15:72208800 C>G maps to ENST00000424560 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr15:72208800 C>G maps to ENST00000424560 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr15:81294797 C>T maps to NM_022566.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr15:81294797 C>T maps to NM_022566.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr17:14110528 G>A maps to NM_001303.3 *444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr17:14110528 G>A maps to NM_001303.3 *444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr18:32400876 C>T maps to NM_001390.4 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr18:32400876 C>T maps to NM_001390.4 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr19:57066550 C>T maps to NM_020828.1 H799H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr19:57066550 C>T maps to NM_020828.1 H799H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr2:74399788 A>G maps to NM_018221.3 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr2:74399788 A>G maps to NM_018221.3 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr20:61048611 G>A maps to NM_080473.4 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr20:61048611 G>A maps to NM_080473.4 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr4:2956204 C>T maps to NM_003703.1 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr4:2956204 C>T maps to NM_003703.1 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr4:20734305 G>A maps to ENST00000382152 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr4:20734305 G>A maps to ENST00000382152 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr4:54327108 G>A maps to NM_001126328.1 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr4:54327108 G>A maps to NM_001126328.1 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr6:5002434 C>G maps to NM_006638.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr6:5002434 C>G maps to NM_006638.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr6:31600742 G>A maps to NM_080686.2 R1431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr6:31600742 G>A maps to NM_080686.2 R1431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr6:31759486 G>A maps to NM_006295.2 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr6:31759486 G>A maps to NM_006295.2 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr7:86556202 G>A maps to NM_001142749.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr7:86556202 G>A maps to NM_001142749.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr8:59764238 C>G maps to NM_014729.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chr8:59764238 C>G maps to NM_014729.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chrX:21550064 C>T maps to NM_014927.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7594-01A-11D-2229-08 chrX:21550064 C>T maps to NM_014927.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr1:21936073 G>A maps to NM_001145658.1 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr1:21936073 G>A maps to NM_001145658.1 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr1:75036914 C>A maps to NM_001002912.4 A1493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr1:75036914 C>A maps to NM_001002912.4 A1493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr1:202406977 A>G maps to ENST00000367270 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr1:202406977 A>G maps to ENST00000367270 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr1:220101746 G>C maps to NM_018713.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr1:220101746 G>C maps to NM_018713.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr1:248569861 G>T maps to NM_030904.1 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr1:248569861 G>T maps to NM_030904.1 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:7683945 C>T maps to ENST00000256861 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:7683945 C>T maps to ENST00000256861 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:17145222 G>A maps to NM_001081.3 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:17145222 G>A maps to NM_001081.3 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:34739280 G>A maps to NM_019619.3 H226H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:34739280 G>A maps to NM_019619.3 H226H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:44053167 C>A maps to NM_001099284.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:44053167 C>A maps to NM_001099284.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:63852351 G>T maps to NM_032199.2 E1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:63852351 G>T maps to NM_032199.2 E1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:94369263 T>C maps to NM_004523.3 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:94369263 T>C maps to NM_004523.3 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:131666136 C>T maps to ENST00000355311 W274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr10:131666136 C>T maps to ENST00000355311 W274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:6007719 G>T maps to NM_001005173.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:6007719 G>T maps to NM_001005173.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:15134051 G>T maps to NM_001031853.3 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:15134051 G>T maps to NM_001031853.3 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:59814416 G>A maps to NM_173801.3 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:59814416 G>A maps to NM_173801.3 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:64502699 C>T did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:64502699 C>T did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:71804596 G>A maps to NM_145309.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:71804596 G>A maps to NM_145309.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:123900457 C>T maps to NM_001004464.1 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:123900457 C>T maps to NM_001004464.1 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:124524632 G>A maps to NM_170601.3 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:124524632 G>A maps to NM_170601.3 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:132307218 C>T maps to NM_002545.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr11:132307218 C>T maps to NM_002545.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:14772148 G>T maps to NM_004963.3 G957G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:14772148 G>T maps to NM_004963.3 G957G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:15035940 G>T maps to NM_001190839.1 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:15035940 G>T maps to NM_001190839.1 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:53171042 A>G maps to NM_015848.4 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:53171042 A>G maps to NM_015848.4 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:56625235 C>A maps to NM_001135195.1 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:56625235 C>A maps to NM_001135195.1 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:57348844 C>T maps to NM_003708.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:57348844 C>T maps to NM_003708.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:71155304 G>T maps to NM_002849.2 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:71155304 G>T maps to NM_002849.2 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:109042421 G>A maps to ENST00000420959 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:109042421 G>A maps to ENST00000420959 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:113384760 T>C maps to NM_006187.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:113384760 T>C maps to NM_006187.2 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:129559165 C>A maps to NM_133448.2 G852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr12:129559165 C>A maps to NM_133448.2 G852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr13:23907283 T>C maps to NM_014363.4 T3577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr13:23907283 T>C maps to NM_014363.4 T3577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr13:46728937 A>T did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr13:46728937 A>T did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr13:84454739 T>A maps to NM_052910.1 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr13:84454739 T>A maps to NM_052910.1 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr14:24769252 C>G maps to NM_174913.1 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr14:24769252 C>G maps to NM_174913.1 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr14:51111688 G>A maps to NM_021818.2 N193N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr14:51111688 G>A maps to NM_021818.2 N193N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr14:59014612 A>T maps to ENST00000354386 A1618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr14:59014612 A>T maps to ENST00000354386 A1618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr14:63417205 C>T maps to NM_139318.3 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr14:63417205 C>T maps to NM_139318.3 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr15:42635315 C>T maps to NM_198141.2 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr15:42635315 C>T maps to NM_198141.2 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr15:93528730 C>T maps to NM_001271.3 Q1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr15:93528730 C>T maps to NM_001271.3 Q1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr16:24366277 C>T maps to NM_006539.3 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr16:24366277 C>T maps to NM_006539.3 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr16:66426223 G>A maps to NM_001795.3 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr16:66426223 G>A maps to NM_001795.3 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr17:13399972 C>T maps to NM_006042.1 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr17:13399972 C>T maps to NM_006042.1 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr17:61958451 G>A maps to NM_002059.3 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr17:61958451 G>A maps to NM_002059.3 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr18:33706799 T>C maps to NM_012319.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr18:33706799 T>C maps to NM_012319.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr18:77107888 C>T maps to NM_198531.3 F934F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr18:77107888 C>T maps to NM_198531.3 F934F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:1484087 G>A maps to NM_017573.3 H369H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:1484087 G>A maps to NM_017573.3 H369H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:9020780 T>G maps to NM_024690.2 R12441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:9020780 T>G maps to NM_024690.2 R12441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:9088991 G>A maps to NM_024690.2 H941H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:9088991 G>A maps to NM_024690.2 H941H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:16504766 G>C maps to ENST00000455140 S654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:16504766 G>C maps to ENST00000455140 S654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:37619743 C>T maps to NM_144689.3 C617C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:37619743 C>T maps to NM_144689.3 C617C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:52376426 G>T maps to NM_032679.2 C272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:52376426 G>T maps to NM_032679.2 C272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:53848881 C>T maps to NM_138374.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:53848881 C>T maps to NM_138374.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:55246765 C>T maps to NM_153443.3 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr19:55246765 C>T maps to NM_153443.3 I332I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:58373461 A>G maps to NM_001130480.2 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:58373461 A>G maps to NM_001130480.2 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:65482680 A>C maps to NM_001005386.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:65482680 A>C maps to NM_001005386.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:80646681 G>T maps to ENST00000402739 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:80646681 G>T maps to ENST00000402739 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:137814024 G>T maps to ENST00000272643 G59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:137814024 G>T maps to ENST00000272643 G59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:162761308 A>G maps to NM_001178015.1 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:162761308 A>G maps to NM_001178015.1 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:170403041 G>A maps to NM_024622.3 Q463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:170403041 G>A maps to NM_024622.3 Q463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:179579025 G>T maps to NM_133378.4 S7581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:179579025 G>T maps to NM_133378.4 S7581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:179616518 A>G maps to ENST00000375038 T3538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:179616518 A>G maps to ENST00000375038 T3538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:222322666 T>C maps to NM_004438.3 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr2:222322666 T>C maps to NM_004438.3 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr20:62493541 C>T maps to NM_080622.3 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr20:62493541 C>T maps to NM_080622.3 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr22:18222144 C>A maps to NM_197966.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr22:18222144 C>A maps to NM_197966.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr22:29090105 C>T did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr22:29090105 C>T did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr22:36661940 G>T maps to NM_145343.2 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr22:36661940 G>T maps to NM_145343.2 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr22:41980049 G>A maps to NM_002676.2 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr22:41980049 G>A maps to NM_002676.2 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr3:112064024 C>G maps to NM_001004196.2 S129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr3:112064024 C>G maps to NM_001004196.2 S129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr4:55604671 C>A maps to NM_000222.2 V960V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr4:55604671 C>A maps to NM_000222.2 V960V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr4:99342514 G>C maps to NM_001100426.1 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr4:99342514 G>C maps to NM_001100426.1 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr4:106473960 C>A maps to ENST00000420470 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr4:106473960 C>A maps to ENST00000420470 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr4:155249305 A>G maps to NM_017639.3 T864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr4:155249305 A>G maps to NM_017639.3 T864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr5:19473640 C>T maps to NM_004934.3 R689R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr5:19473640 C>T maps to NM_004934.3 R689R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr6:28121668 G>C maps to NM_006298.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr6:28121668 G>C maps to NM_006298.2 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr6:42574325 G>A did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr6:42574325 G>A did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr6:130762040 A>T maps to NM_052913.2 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr6:130762040 A>T maps to NM_052913.2 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr6:133785941 T>G maps to ENST00000452339 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr6:133785941 T>G maps to ENST00000452339 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr6:138584500 G>T maps to NM_020340.4 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr6:138584500 G>T maps to NM_020340.4 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr7:2265107 C>A maps to NM_003550.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr7:2265107 C>A maps to NM_003550.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr7:83610668 A>T maps to NM_006080.2 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr7:83610668 A>T maps to NM_006080.2 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr7:92300835 C>T maps to NM_001145306.1 W184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr7:92300835 C>T maps to NM_001145306.1 W184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr7:131191356 G>A maps to NM_001018111.2 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr7:131191356 G>A maps to NM_001018111.2 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr7:148876805 G>T maps to NM_170686.2 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr7:148876805 G>T maps to NM_170686.2 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:2886889 G>T maps to NM_033225.5 C2602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:2886889 G>T maps to NM_033225.5 C2602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:27099980 C>A maps to NM_030795.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:27099980 C>A maps to NM_030795.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:35583802 G>A maps to ENST00000416672 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:35583802 G>A maps to ENST00000416672 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:55534122 C>T maps to NM_006269.1 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:55534122 C>T maps to NM_006269.1 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:87242275 A>G maps to NM_138817.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:87242275 A>G maps to NM_138817.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:89068363 C>T maps to NM_005941.4 K455K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:89068363 C>T maps to NM_005941.4 K455K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:92998474 G>T maps to NM_175634.2 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr8:92998474 G>T maps to NM_175634.2 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr9:84607187 C>A maps to NM_001001670.2 I601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr9:84607187 C>A maps to NM_001001670.2 I601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr9:135073846 G>A maps to NM_032536.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr9:135073846 G>A maps to NM_032536.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chrX:66931442 C>T maps to NM_000044.2 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chrX:66931442 C>T maps to NM_000044.2 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:3418408 C>G maps to ENST00000452816 T830T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:3418408 C>G maps to ENST00000452816 T830T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:79093944 T>C maps to NM_006820.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:79093944 T>C maps to NM_006820.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:79385873 A>T maps to NM_022159.3 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:79385873 A>T maps to NM_022159.3 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:89271324 A>T maps to NM_006256.2 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:89271324 A>T maps to NM_006256.2 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:94964202 G>T maps to ENST00000454898 G502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:94964202 G>T maps to ENST00000454898 G502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:157659663 C>T maps to NM_052939.3 T578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:157659663 C>T maps to NM_052939.3 T578T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:163317626 C>T maps to NM_145697.2 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:163317626 C>T maps to NM_145697.2 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:176671755 G>T maps to NM_020318.2 G1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:176671755 G>T maps to NM_020318.2 G1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:196697649 C>A maps to NM_000186.3 S804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:196697649 C>A maps to NM_000186.3 S804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:196709851 T>A maps to NM_000186.3 G962G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:196709851 T>A maps to NM_000186.3 G962G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:203140616 G>C maps to NM_004997.2 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:203140616 G>C maps to NM_004997.2 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:240351555 C>G maps to ENST00000406993 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr1:240351555 C>G maps to ENST00000406993 V803V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr10:16982124 G>A maps to NM_001081.3 L1818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr10:16982124 G>A maps to NM_001081.3 L1818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr10:64415347 C>G maps to NM_199452.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr10:64415347 C>G maps to NM_199452.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr10:94773978 A>G maps to NM_019053.4 G708G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr10:94773978 A>G maps to NM_019053.4 G708G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr10:118355781 C>G maps to NM_006229.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr10:118355781 C>G maps to NM_006229.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr11:45277358 C>G maps to NM_020826.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr11:45277358 C>G maps to NM_020826.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr11:68665461 G>T maps to NM_181514.1 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr11:68665461 G>T maps to NM_181514.1 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr11:94533289 G>T maps to NM_130847.2 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr11:94533289 G>T maps to NM_130847.2 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr12:13768123 A>G maps to NM_000834.3 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr12:13768123 A>G maps to NM_000834.3 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr12:21327509 G>C did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr12:21327509 G>C did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr12:52842694 C>T maps to NM_005555.3 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr12:52842694 C>T maps to NM_005555.3 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr12:78522566 C>T maps to NM_014903.4 D1454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr12:78522566 C>T maps to NM_014903.4 D1454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr13:99087857 G>C maps to NM_005766.2 V724V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr13:99087857 G>C maps to NM_005766.2 V724V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr14:24652821 G>A maps to ENST00000458132 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr14:24652821 G>A maps to ENST00000458132 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr14:36128344 G>A maps to NM_194301.2 R1290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr14:36128344 G>A maps to NM_194301.2 R1290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr14:95574698 T>G maps to NM_177438.2 R800R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr14:95574698 T>G maps to NM_177438.2 R800R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr16:3024068 A>T maps to NM_004203.4 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr16:3024068 A>T maps to NM_004203.4 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr16:23391743 C>T maps to ENST00000307331 I560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr16:23391743 C>T maps to ENST00000307331 I560I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr16:28895896 G>T maps to NM_173201.3 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr16:28895896 G>T maps to NM_173201.3 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr16:30977520 C>T maps to NM_014712.1 P773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr16:30977520 C>T maps to NM_014712.1 P773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr16:67201121 G>A maps to NM_001040667.2 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr16:67201121 G>A maps to NM_001040667.2 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr17:6927485 C>G maps to NM_181844.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr17:6927485 C>G maps to NM_181844.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr17:10432119 C>A maps to NM_017534.5 E1211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr17:10432119 C>A maps to NM_017534.5 E1211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr17:21319643 G>T maps to NM_021012.4 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr17:21319643 G>T maps to NM_021012.4 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr18:5891792 C>G maps to NM_001080209.1 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr18:5891792 C>G maps to NM_001080209.1 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr18:7955362 T>A maps to NM_001105244.1 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr18:7955362 T>A maps to NM_001105244.1 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr19:11943667 A>G maps to NM_152357.2 E559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr19:11943667 A>G maps to NM_152357.2 E559E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr19:54692189 C>T maps to NM_024298.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr19:54692189 C>T maps to NM_024298.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr19:55915801 G>A maps to NM_014501.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr19:55915801 G>A maps to NM_014501.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr19:56901747 T>C maps to NM_144690.1 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr19:56901747 T>C maps to NM_144690.1 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr19:58639937 C>G maps to NM_024620.3 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr19:58639937 C>G maps to NM_024620.3 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:21234731 C>A maps to NM_000384.2 E1670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:21234731 C>A maps to NM_000384.2 E1670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:42472705 A>G maps to NM_019063.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:42472705 A>G maps to NM_019063.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:109473415 G>T maps to NM_144978.1 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:109473415 G>T maps to NM_144978.1 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:128409253 A>G maps to NM_005291.2 K343K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:128409253 A>G maps to NM_005291.2 K343K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:138169329 A>C maps to ENST00000272643 G949G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:138169329 A>C maps to ENST00000272643 G949G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:158272442 G>T maps to NM_004288.4 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:158272442 G>T maps to NM_004288.4 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:160833231 C>T did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:160833231 C>T did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:163027569 G>A maps to NM_004460.2 H734H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:163027569 G>A maps to NM_004460.2 H734H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:185800593 G>T maps to NM_194250.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:185800593 G>T maps to NM_194250.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:196578253 G>A maps to NM_001127257.1 W558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:196578253 G>A maps to NM_001127257.1 W558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:223554123 A>T maps to NM_058165.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:223554123 A>T maps to NM_058165.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:228855880 A>T maps to NM_001142644.1 P1598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr2:228855880 A>T maps to NM_001142644.1 P1598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr20:1918051 G>T maps to ENST00000400068 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr20:1918051 G>T maps to ENST00000400068 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr20:20177326 G>A maps to ENST00000389655 R571R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr20:20177326 G>A maps to ENST00000389655 R571R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr20:36869161 A>G maps to NM_001029864.1 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr20:36869161 A>G maps to NM_001029864.1 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr20:62191626 G>A maps to NM_001037335.2 I2518I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr20:62191626 G>A maps to NM_001037335.2 I2518I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:17051330 C>T maps to NM_001144382.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:17051330 C>T maps to NM_001144382.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:36545897 A>T maps to NM_003149.1 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:36545897 A>T maps to NM_003149.1 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:46479620 C>A did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:46479620 C>A did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:49142160 C>G maps to NM_005051.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:49142160 C>G maps to NM_005051.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:111632431 C>T maps to NM_001134438.1 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:111632431 C>T maps to NM_001134438.1 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:121342099 C>A maps to NM_016298.3 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:121342099 C>A maps to NM_016298.3 A608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:160964155 A>G maps to ENST00000472947 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:160964155 A>G maps to ENST00000472947 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:164908114 T>A maps to NM_014926.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:164908114 T>A maps to NM_014926.2 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:192125892 C>T maps to NM_021032.4 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr3:192125892 C>T maps to NM_021032.4 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:59330 A>T maps to NM_182524.2 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:59330 A>T maps to NM_182524.2 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:6302727 G>C maps to NM_006005.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:6302727 G>C maps to NM_006005.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:55161417 G>T maps to ENST00000507166 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:55161417 G>T maps to ENST00000507166 L843L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:69184562 G>A maps to NM_001031732.2 R568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:69184562 G>A maps to NM_001031732.2 R568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:69519825 G>A maps to NM_001076.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:69519825 G>A maps to NM_001076.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:77003167 T>C maps to NM_001130016.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:77003167 T>C maps to NM_001130016.1 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:114179510 T>C maps to NM_001148.4 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:114179510 T>C maps to NM_001148.4 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:123814171 C>A maps to NM_007083.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:123814171 C>A maps to NM_007083.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:134072305 C>A maps to NM_032961.1 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:134072305 C>A maps to NM_032961.1 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:151504975 C>A maps to NM_006439.4 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:151504975 C>A maps to NM_006439.4 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:156632129 C>A maps to NM_001130684.1 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:156632129 C>A maps to NM_001130684.1 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:164247553 G>T maps to NM_000909.4 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr4:164247553 G>T maps to NM_000909.4 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr5:11082942 G>A maps to NM_001332.2 R885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr5:11082942 G>A maps to NM_001332.2 R885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr5:21752112 G>T maps to NM_004061.3 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr5:21752112 G>T maps to NM_004061.3 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr5:26988326 C>A maps to NM_016279.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr5:26988326 C>A maps to NM_016279.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr5:35965517 C>T maps to NM_152404.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr5:35965517 C>T maps to NM_152404.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:18148146 C>G did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:18148146 C>G did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:22570037 G>T maps to NM_138574.2 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:22570037 G>T maps to NM_138574.2 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:26451999 A>T maps to NM_006994.4 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:26451999 A>T maps to NM_006994.4 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:29364490 C>G maps to NM_013936.3 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:29364490 C>G maps to NM_013936.3 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:41303864 G>A maps to NM_004828.3 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:41303864 G>A maps to NM_004828.3 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:51768525 C>T did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:51768525 C>T did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:62442585 C>A did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:62442585 C>A did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:83767584 T>G maps to NM_198920.1 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:83767584 T>G maps to NM_198920.1 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:90660480 A>G maps to NM_001170794.1 Y448Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:90660480 A>G maps to NM_001170794.1 Y448Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:119337959 A>T maps to NM_024581.4 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:119337959 A>T maps to NM_024581.4 I494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:129687472 G>T maps to NM_000426.3 L1609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:129687472 G>T maps to NM_000426.3 L1609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:132059243 T>C maps to NM_005021.3 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:132059243 T>C maps to NM_005021.3 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:167595299 C>T maps to NM_001145121.1 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr6:167595299 C>T maps to NM_001145121.1 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr7:8272243 G>A maps to ENST00000422063 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr7:8272243 G>A maps to ENST00000422063 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr7:83021871 T>G maps to NM_012431.2 R556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr7:83021871 T>G maps to NM_012431.2 R556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr7:117251689 T>A maps to NM_000492.3 L1065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr7:117251689 T>A maps to NM_000492.3 L1065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr7:137790054 G>T maps to NM_005989.3 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr7:137790054 G>T maps to NM_005989.3 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr7:150814820 C>T maps to NM_031946.4 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr7:150814820 C>T maps to NM_031946.4 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr8:54147355 G>T maps to NM_000912.3 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr8:54147355 G>T maps to NM_000912.3 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr8:61765574 C>T maps to NM_017780.2 D2097D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr8:61765574 C>T maps to NM_017780.2 D2097D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr8:70512982 G>T maps to NM_001128206.1 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr8:70512982 G>T maps to NM_001128206.1 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr8:77764097 G>A maps to NM_024721.4 Q1647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr8:77764097 G>A maps to NM_024721.4 Q1647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr8:103326145 T>C did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr8:103326145 T>C did not map to a codon.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr8:117782553 G>T maps to NM_032334.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr8:117782553 G>T maps to NM_032334.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr9:26861106 G>A maps to NM_024828.3 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr9:26861106 G>A maps to NM_024828.3 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr9:80880326 A>C maps to NM_001098802.1 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr9:80880326 A>C maps to NM_001098802.1 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr9:111970305 C>T maps to NM_019114.3 E592E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr9:111970305 C>T maps to NM_019114.3 E592E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr9:113562628 C>A maps to ENST00000189978 Y663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chr9:113562628 C>A maps to ENST00000189978 Y663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chrX:28807463 A>T maps to NM_014271.3 K2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chrX:28807463 A>T maps to NM_014271.3 K2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chrX:35993267 T>G maps to NM_152632.3 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chrX:35993267 T>G maps to NM_152632.3 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chrX:139865919 C>T maps to NM_004065.2 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F7-7848-01A-11D-2129-08 chrX:139865919 C>T maps to NM_004065.2 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr1:32148955 G>A maps to NM_001856.3 A798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr1:32148955 G>A maps to NM_001856.3 A798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr1:156268970 T>G maps to NM_001004319.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr1:156268970 T>G maps to NM_001004319.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr1:158549569 C>T maps to NM_001004477.1 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr1:158549569 C>T maps to NM_001004477.1 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr1:236341830 A>T maps to NM_003272.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr1:236341830 A>T maps to NM_003272.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr10:117884985 C>T maps to NM_005264.4 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr10:117884985 C>T maps to NM_005264.4 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr11:18735567 G>T maps to NM_173588.3 Y642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr11:18735567 G>T maps to NM_173588.3 Y642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr11:22257815 C>A maps to NM_213599.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr11:22257815 C>A maps to NM_213599.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr11:123848323 G>A maps to NM_001004474.1 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr11:123848323 G>A maps to NM_001004474.1 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr12:34179306 C>T maps to NM_032834.3 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr12:34179306 C>T maps to NM_032834.3 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr14:21873942 C>T maps to NM_001170629.1 P996P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr14:21873942 C>T maps to NM_001170629.1 P996P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr14:93408121 G>A maps to NM_014216.4 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr14:93408121 G>A maps to NM_014216.4 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr14:105409646 G>C maps to NM_138420.2 L4047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr14:105409646 G>C maps to NM_138420.2 L4047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr15:33962689 T>G maps to NM_001036.3 V1931V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr15:33962689 T>G maps to NM_001036.3 V1931V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr15:50763973 G>C maps to NM_005154.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr15:50763973 G>C maps to NM_005154.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr15:65793045 G>A maps to NM_197960.2 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr15:65793045 G>A maps to NM_197960.2 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr15:72119039 G>A maps to ENST00000424560 Q2581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr15:72119039 G>A maps to ENST00000424560 Q2581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr17:5998440 C>T maps to NM_015253.1 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr17:5998440 C>T maps to NM_015253.1 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr18:9257776 G>T maps to NM_015208.3 S1504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr18:9257776 G>T maps to NM_015208.3 S1504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr19:17768989 C>T maps to ENST00000428389 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr19:17768989 C>T maps to ENST00000428389 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr2:175252491 G>A maps to NM_004882.3 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr2:175252491 G>A maps to NM_004882.3 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr3:9691416 C>A maps to NM_001077525.2 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr3:9691416 C>A maps to NM_001077525.2 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr3:17056294 C>T maps to NM_001144382.1 P966P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr3:17056294 C>T maps to NM_001144382.1 P966P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr3:172165819 G>A maps to NM_198407.2 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr3:172165819 G>A maps to NM_198407.2 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr4:3318625 G>A maps to NM_198229.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr4:3318625 G>A maps to NM_198229.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr4:187525007 C>A maps to ENST00000260147 E3561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr4:187525007 C>A maps to ENST00000260147 E3561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr5:35659167 C>T maps to NM_024867.3 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr5:35659167 C>T maps to NM_024867.3 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr5:88027716 C>T maps to NM_002397.4 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr5:88027716 C>T maps to NM_002397.4 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr5:140257231 G>A maps to NM_018903.2 A725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr5:140257231 G>A maps to NM_018903.2 A725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr5:170148873 C>T maps to NM_001034837.1 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr5:170148873 C>T maps to NM_001034837.1 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr6:32097031 G>A maps to NM_022110.3 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr6:32097031 G>A maps to NM_022110.3 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr6:129649433 G>A maps to NM_000426.3 P1396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr6:129649433 G>A maps to NM_000426.3 P1396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr6:134210906 G>A maps to NM_003206.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr6:134210906 G>A maps to NM_003206.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr7:883125 G>A maps to ENST00000456758 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr7:883125 G>A maps to ENST00000456758 S267S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-H7-7774-01A-21D-2078-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-H7-7774-01A-21D-2078-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr7:57188353 A>G maps to NM_033273.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr7:57188353 A>G maps to NM_033273.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr7:150389490 G>A maps to NM_015660.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr7:150389490 G>A maps to NM_015660.2 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr8:73480223 C>T maps to NM_004770.2 N85N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr8:73480223 C>T maps to NM_004770.2 N85N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr8:110412467 T>C maps to ENST00000426474 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr8:110412467 T>C maps to ENST00000426474 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr8:110535535 C>T maps to ENST00000426474 V4136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr8:110535535 C>T maps to ENST00000426474 V4136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr8:113353855 G>A maps to NM_198123.1 R2168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr8:113353855 G>A maps to NM_198123.1 R2168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr8:117658785 C>A maps to ENST00000411422 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr8:117658785 C>A maps to ENST00000411422 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr8:144991067 C>T maps to NM_201380.2 T4444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr8:144991067 C>T maps to NM_201380.2 T4444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr9:113170973 C>T maps to ENST00000374463 W2305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chr9:113170973 C>T maps to ENST00000374463 W2305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chrX:49127006 T>A maps to NM_033215.4 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chrX:49127006 T>A maps to NM_033215.4 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chrX:53577937 C>A maps to ENST00000276009 R3105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chrX:53577937 C>A maps to ENST00000276009 R3105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chrX:123196816 C>A maps to NM_001042750.1 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chrX:123196816 C>A maps to NM_001042750.1 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chrX:137715118 G>A maps to NM_001139500.1 H220H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H7-7774-01A-21D-2078-08 chrX:137715118 G>A maps to NM_001139500.1 H220H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr1:22178185 G>A maps to NM_005529.5 A2337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr1:22178185 G>A maps to NM_005529.5 A2337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr1:24434493 G>A maps to ENST00000330966 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr1:24434493 G>A maps to ENST00000330966 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr1:27276604 G>A maps to NM_152365.2 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr1:27276604 G>A maps to NM_152365.2 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr1:169390627 T>C maps to ENST00000367806 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr1:169390627 T>C maps to ENST00000367806 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr1:216680337 T>C maps to NM_001438.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr1:216680337 T>C maps to NM_001438.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr11:56511134 C>T maps to NM_001005284.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr11:56511134 C>T maps to NM_001005284.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr11:65547194 G>A maps to NM_138368.3 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr11:65547194 G>A maps to NM_138368.3 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr11:76255466 G>A maps to ENST00000393457 P959P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr11:76255466 G>A maps to ENST00000393457 P959P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr11:95569428 G>A maps to NM_016156.5 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr11:95569428 G>A maps to NM_016156.5 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr12:57145980 T>A maps to NM_000946.2 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr12:57145980 T>A maps to NM_000946.2 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr12:111993686 C>A maps to NM_002973.3 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr12:111993686 C>A maps to NM_002973.3 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr12:113744330 C>G maps to NM_024959.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr12:113744330 C>G maps to NM_024959.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr13:42393506 G>A maps to NM_015058.1 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr13:42393506 G>A maps to NM_015058.1 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr13:53422220 C>T maps to NM_002590.2 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr13:53422220 C>T maps to NM_002590.2 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr13:67801102 A>T maps to NM_203487.2 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr13:67801102 A>T maps to NM_203487.2 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr13:99061620 G>T maps to NM_005766.2 E482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr13:99061620 G>T maps to NM_005766.2 E482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr13:110831717 G>A maps to NM_001845.4 P748P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr13:110831717 G>A maps to NM_001845.4 P748P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr13:113210455 G>A maps to NM_006322.4 Q211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr13:113210455 G>A maps to NM_006322.4 Q211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr15:42457993 C>T maps to ENST00000348544 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr15:42457993 C>T maps to ENST00000348544 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr15:64204145 C>T maps to NM_014326.3 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr15:64204145 C>T maps to NM_014326.3 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr15:73616246 G>C maps to NM_005477.2 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr15:73616246 G>C maps to NM_005477.2 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr15:75641449 C>G maps to NM_024608.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr15:75641449 C>G maps to NM_024608.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr16:4714766 G>T maps to NM_015246.2 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr16:4714766 G>T maps to NM_015246.2 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr16:30536710 G>A maps to NM_024671.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr16:30536710 G>A maps to NM_024671.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr16:56503928 G>A maps to NM_018233.3 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr16:56503928 G>A maps to NM_018233.3 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr16:67487538 G>A maps to NM_004691.4 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr16:67487538 G>A maps to NM_004691.4 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr16:67578270 G>A maps to NM_001193523.1 T910T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr16:67578270 G>A maps to NM_001193523.1 T910T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr16:81193336 G>A maps to NM_052892.3 D1262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr16:81193336 G>A maps to NM_052892.3 D1262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr17:2597271 G>C maps to NM_015229.3 Y1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr17:2597271 G>C maps to NM_015229.3 Y1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr17:16638737 G>A maps to NM_014695.1 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr17:16638737 G>A maps to NM_014695.1 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr17:43923891 C>T maps to NM_175882.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr17:43923891 C>T maps to NM_175882.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr17:79478625 C>A maps to NM_001614.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr17:79478625 C>A maps to NM_001614.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr19:7831596 C>G maps to NM_014257.4 Y280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr19:7831596 C>G maps to NM_014257.4 Y280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr19:10090690 G>A maps to NM_015719.3 F879F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr19:10090690 G>A maps to NM_015719.3 F879F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr19:10923010 T>C maps to NM_001005361.2 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr19:10923010 T>C maps to NM_001005361.2 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr19:16613910 C>T maps to NM_032207.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr19:16613910 C>T maps to NM_032207.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr19:39361378 G>A maps to NM_001195833.1 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr19:39361378 G>A maps to NM_001195833.1 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr2:27499676 C>A maps to NM_173650.1 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr2:27499676 C>A maps to NM_173650.1 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr2:232393434 G>C maps to NM_006056.4 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr2:232393434 G>C maps to NM_006056.4 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr3:4725401 G>T maps to ENST00000356617 E1136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr3:4725401 G>T maps to ENST00000356617 E1136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr3:164754248 C>A maps to NM_001041.3 G815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr3:164754248 C>A maps to NM_001041.3 G815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr4:113462063 T>A maps to NM_018392.4 T1941T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr4:113462063 T>A maps to NM_018392.4 T1941T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr5:19483517 C>A maps to NM_004934.3 E592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr5:19483517 C>A maps to NM_004934.3 E592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr5:127614516 G>C maps to NM_001999.3 L2385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr5:127614516 G>C maps to NM_001999.3 L2385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr5:134782554 G>A maps to NM_130848.2 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr5:134782554 G>A maps to NM_130848.2 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr6:159050834 G>A maps to NM_020823.1 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr6:159050834 G>A maps to NM_020823.1 S559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr6:169640558 C>G maps to NM_003247.2 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr6:169640558 C>G maps to NM_003247.2 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr7:4839062 C>T maps to NM_018059.4 A1058A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr7:4839062 C>T maps to NM_018059.4 A1058A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr7:15652016 A>G maps to NM_005924.4 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr7:15652016 A>G maps to NM_005924.4 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr7:21639562 G>T maps to NM_003777.3 P942P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr7:21639562 G>T maps to NM_003777.3 P942P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr7:138603741 C>T maps to NM_001164665.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr7:138603741 C>T maps to NM_001164665.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr8:124204206 C>T maps to NM_032899.4 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr8:124204206 C>T maps to NM_032899.4 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr8:144996308 A>G maps to NM_201380.2 H2697H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chr8:144996308 A>G maps to NM_201380.2 H2697H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chrX:44922693 C>T maps to NM_021140.2 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chrX:44922693 C>T maps to NM_021140.2 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chrX:70823684 G>C maps to NM_052957.4 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7229-01A-11D-2012-08 chrX:70823684 G>C maps to NM_052957.4 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr1:62921090 A>G maps to ENST00000371140 D2139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr1:62921090 A>G maps to ENST00000371140 D2139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr1:159890212 G>A maps to ENST00000368096 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr1:159890212 G>A maps to ENST00000368096 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr1:190067945 C>T maps to NM_199051.1 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr1:190067945 C>T maps to NM_199051.1 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr11:49227671 A>G maps to NM_004476.1 N57N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr11:49227671 A>G maps to NM_004476.1 N57N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr11:61511762 C>G maps to NM_006133.2 A977A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr11:61511762 C>G maps to NM_006133.2 A977A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr12:7639149 G>A maps to NM_004244.4 H801H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr12:7639149 G>A maps to NM_004244.4 H801H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr15:81282114 C>T maps to NM_015154.1 W6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr15:81282114 C>T maps to NM_015154.1 W6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr15:93007599 C>T maps to NM_006011.3 C371C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr15:93007599 C>T maps to NM_006011.3 C371C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr17:15620348 C>T maps to NM_020652.2 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr17:15620348 C>T maps to NM_020652.2 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr17:36485311 C>A maps to ENST00000398597 P1381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr17:36485311 C>A maps to ENST00000398597 P1381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr17:38711203 G>A maps to NM_001838.3 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr17:38711203 G>A maps to NM_001838.3 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr19:22941471 A>G maps to ENST00000397104 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr19:22941471 A>G maps to ENST00000397104 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr2:152276854 C>T maps to NM_018151.4 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr2:152276854 C>T maps to NM_018151.4 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr2:155252509 C>T maps to NM_052917.2 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr2:155252509 C>T maps to NM_052917.2 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr2:232079576 C>T maps to ENST00000359743 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr2:232079576 C>T maps to ENST00000359743 Q71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr20:43977028 C>T did not map to a codon.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr20:43977028 C>T did not map to a codon.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr21:43547901 C>A maps to NM_173568.3 L1345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr21:43547901 C>A maps to NM_173568.3 L1345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr22:16267044 T>C maps to NM_001136213.1 E468E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr22:16267044 T>C maps to NM_001136213.1 E468E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr22:35726366 C>T maps to ENST00000451197 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr22:35726366 C>T maps to ENST00000451197 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr4:184626158 C>A maps to NM_021942.4 I997I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr4:184626158 C>A maps to NM_021942.4 I997I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr4:187179173 G>T did not map to a codon.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr4:187179173 G>T did not map to a codon.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr7:48318539 A>G maps to NM_152701.3 T2583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr7:48318539 A>G maps to NM_152701.3 T2583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr7:150936505 G>A maps to NM_003078.3 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chr7:150936505 G>A maps to NM_003078.3 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chrX:10535568 C>A maps to NM_001193277.1 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chrX:10535568 C>A maps to NM_001193277.1 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chrX:44922693 C>T maps to NM_021140.2 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chrX:44922693 C>T maps to NM_021140.2 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chrX:84526032 G>A maps to ENST00000360700 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chrX:84526032 G>A maps to ENST00000360700 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chrX:109696371 G>T maps to NM_020769.2 G843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7753-01A-11D-2078-08 chrX:109696371 G>T maps to NM_020769.2 G843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr1:156130750 C>T maps to NM_022367.3 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr1:156130750 C>T maps to NM_022367.3 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr1:158549197 A>C maps to NM_001004477.1 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr1:158549197 A>C maps to NM_001004477.1 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr1:236912509 C>T maps to NM_001103.2 G534G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr1:236912509 C>T maps to NM_001103.2 G534G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr10:123970458 G>A maps to NM_206862.2 T2173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr10:123970458 G>A maps to NM_206862.2 T2173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr11:22281075 C>T maps to NM_213599.2 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr11:22281075 C>T maps to NM_213599.2 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr11:130275689 G>A maps to NM_007037.4 D811D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr11:130275689 G>A maps to NM_007037.4 D811D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr12:6981423 G>A maps to NM_032641.3 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr12:6981423 G>A maps to NM_032641.3 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr14:33292160 G>A maps to NM_004274.4 S1714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr14:33292160 G>A maps to NM_004274.4 S1714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr15:42169044 G>A maps to ENST00000320955 G1271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr15:42169044 G>A maps to ENST00000320955 G1271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr15:43931100 C>T did not map to a codon.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr15:43931100 C>T did not map to a codon.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr16:24366271 G>A maps to NM_006539.3 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr16:24366271 G>A maps to NM_006539.3 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr16:31510703 G>A maps to NM_022744.2 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr16:31510703 G>A maps to NM_022744.2 D173D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr18:21140391 G>A maps to NM_000271.4 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr18:21140391 G>A maps to NM_000271.4 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr2:43755034 G>A maps to ENST00000330266 L1120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr2:43755034 G>A maps to ENST00000330266 L1120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr2:121989536 G>A maps to NM_014553.2 H402H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr2:121989536 G>A maps to NM_014553.2 H402H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr20:18165391 A>C maps to NM_020536.4 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr20:18165391 A>C maps to NM_020536.4 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr20:47567891 C>T maps to NM_006420.2 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr20:47567891 C>T maps to NM_006420.2 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr20:52570171 C>T maps to NM_003657.2 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr20:52570171 C>T maps to NM_003657.2 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr21:38858908 C>T maps to NM_001396.3 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr21:38858908 C>T maps to NM_001396.3 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr3:8794893 G>A maps to NM_000916.3 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr3:8794893 G>A maps to NM_000916.3 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr3:50418477 T>C maps to ENST00000435965 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr3:50418477 T>C maps to ENST00000435965 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr4:25258217 A>G maps to NM_018323.3 K226K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr4:25258217 A>G maps to NM_018323.3 K226K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr4:38776632 C>A maps to NM_030956.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr4:38776632 C>A maps to NM_030956.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr4:72629178 G>T maps to ENST00000504199 S235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr4:72629178 G>T maps to ENST00000504199 S235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr4:123176338 T>C maps to NM_015312.3 V2093V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr4:123176338 T>C maps to NM_015312.3 V2093V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr9:5065040 G>A did not map to a codon.
Sequencing variant TCGA-HD-7754-01A-11D-2078-08 chr9:5065040 G>A did not map to a codon.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr1:11708855 C>T maps to NM_012168.4 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr1:11708855 C>T maps to NM_012168.4 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr1:156509199 G>A maps to NM_178229.4 Q1008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr1:156509199 G>A maps to NM_178229.4 Q1008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr11:5068240 C>G maps to NM_001001916.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr11:5068240 C>G maps to NM_001001916.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr12:8994101 C>T maps to NM_144670.3 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr12:8994101 C>T maps to NM_144670.3 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr14:24545395 G>A maps to NM_006032.2 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr14:24545395 G>A maps to NM_006032.2 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr16:83813621 C>T maps to ENST00000268613 D577D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr16:83813621 C>T maps to ENST00000268613 D577D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr19:4219649 A>T maps to ENST00000262970 T1112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr19:4219649 A>T maps to ENST00000262970 T1112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr2:102968038 G>A maps to NM_016232.4 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr2:102968038 G>A maps to NM_016232.4 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr22:37770212 G>A maps to NM_052906.3 H454H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr22:37770212 G>A maps to NM_052906.3 H454H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr3:155215155 A>T maps to ENST00000340059 L604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr3:155215155 A>T maps to ENST00000340059 L604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr4:515514 C>T maps to NM_001127178.1 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr4:515514 C>T maps to NM_001127178.1 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr5:115151944 G>A maps to NM_001801.2 Y50Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr5:115151944 G>A maps to NM_001801.2 Y50Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr7:2632712 C>T maps to NM_152558.3 C434C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr7:2632712 C>T maps to NM_152558.3 C434C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr7:107314735 A>G maps to NM_000441.1 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr7:107314735 A>G maps to NM_000441.1 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr8:103293650 C>T maps to NM_015902.4 E1931E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr8:103293650 C>T maps to NM_015902.4 E1931E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr9:126777640 G>A maps to NM_004789.3 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7831-01A-11D-2129-08 chr9:126777640 G>A maps to NM_004789.3 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr1:10356658 C>T maps to ENST00000377086 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr1:10356658 C>T maps to ENST00000377086 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr1:11893657 G>A maps to ENST00000376496 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr1:11893657 G>A maps to ENST00000376496 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr1:75038684 C>A maps to NM_001002912.4 V903V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr1:75038684 C>A maps to NM_001002912.4 V903V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr1:179354443 A>G maps to NM_144696.4 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr1:179354443 A>G maps to NM_144696.4 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr1:247921165 G>A maps to NM_012353.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr1:247921165 G>A maps to NM_012353.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr11:56085985 C>T maps to NM_001005202.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr11:56085985 C>T maps to NM_001005202.1 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr11:100141897 C>T maps to NM_014361.2 R747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr11:100141897 C>T maps to NM_014361.2 R747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr12:9265042 C>T maps to NM_000014.4 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr12:9265042 C>T maps to NM_000014.4 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr12:40158309 G>A maps to NM_052885.3 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr12:40158309 G>A maps to NM_052885.3 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr12:54396310 C>T maps to NM_006897.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr12:54396310 C>T maps to NM_006897.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr12:63544544 G>A maps to NM_000706.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr12:63544544 G>A maps to NM_000706.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr13:88329718 G>A maps to NM_015567.1 R692R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr13:88329718 G>A maps to NM_015567.1 R692R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr13:113730377 C>T maps to NM_001112732.1 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr13:113730377 C>T maps to NM_001112732.1 I526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr14:24114423 G>A maps to NM_182908.4 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr14:24114423 G>A maps to NM_182908.4 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr15:75974678 C>T maps to NM_001897.4 Q1635Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr15:75974678 C>T maps to NM_001897.4 Q1635Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr17:8411914 G>A maps to ENST00000360416 A1057A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr17:8411914 G>A maps to ENST00000360416 A1057A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr17:43545613 T>A maps to NM_014798.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr17:43545613 T>A maps to NM_014798.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr17:72923777 A>T maps to NM_178160.2 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr17:72923777 A>T maps to NM_178160.2 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr18:19995818 T>C maps to NM_172241.2 E652E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr18:19995818 T>C maps to NM_172241.2 E652E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr19:18731325 C>T maps to NM_012109.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr19:18731325 C>T maps to NM_012109.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr19:53959872 C>T maps to NM_001008401.3 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr19:53959872 C>T maps to NM_001008401.3 S704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr2:5833020 C>T maps to NM_003108.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr2:5833020 C>T maps to NM_003108.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr2:179588169 A>T maps to NM_133378.4 S5975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr2:179588169 A>T maps to NM_133378.4 S5975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr2:234198585 G>A maps to ENST00000392018 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr2:234198585 G>A maps to ENST00000392018 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr2:239342261 G>A maps to NM_001040445.1 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr2:239342261 G>A maps to NM_001040445.1 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr20:62701951 C>A maps to NM_003195.4 C261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr20:62701951 C>A maps to NM_003195.4 C261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr22:24086331 G>A maps to NM_021916.2 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr22:24086331 G>A maps to NM_021916.2 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr22:33670598 G>A maps to NM_133642.3 F695F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr22:33670598 G>A maps to NM_133642.3 F695F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr22:40061517 G>A maps to NM_021096.3 A1289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr22:40061517 G>A maps to NM_021096.3 A1289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr4:71346724 C>T maps to NM_152291.2 H88H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr4:71346724 C>T maps to NM_152291.2 H88H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr4:141543480 C>T maps to NM_015130.2 E1223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr4:141543480 C>T maps to NM_015130.2 E1223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr5:128977611 C>T maps to NM_133638.3 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr5:128977611 C>T maps to NM_133638.3 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr5:149216429 C>T maps to NM_133263.3 F804F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr5:149216429 C>T maps to NM_133263.3 F804F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr6:86259571 T>C maps to NM_153816.3 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr6:86259571 T>C maps to NM_153816.3 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr7:40134009 C>T maps to NM_003718.4 Q1324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr7:40134009 C>T maps to NM_003718.4 Q1324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr7:142605865 G>T maps to NM_019841.4 P668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chr7:142605865 G>T maps to NM_019841.4 P668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chrX:30260590 G>A maps to NM_002367.3 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7832-01A-11D-2129-08 chrX:30260590 G>A maps to NM_002367.3 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr1:34192215 C>T maps to ENST00000373381 K773K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr1:34192215 C>T maps to ENST00000373381 K773K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr11:70222702 T>C maps to NM_003626.2 D1127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr11:70222702 T>C maps to NM_003626.2 D1127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr11:124637179 T>C maps to ENST00000374979 K524K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr11:124637179 T>C maps to ENST00000374979 K524K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr12:111099132 C>A maps to NM_001040107.1 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr12:111099132 C>A maps to NM_001040107.1 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr16:624736 G>A maps to NM_148920.1 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr16:624736 G>A maps to NM_148920.1 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr16:30735403 G>A maps to NM_006662.2 S1553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr16:30735403 G>A maps to NM_006662.2 S1553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr16:67434867 G>A maps to NM_013304.2 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr16:67434867 G>A maps to NM_013304.2 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr17:7574033 C>A did not map to a codon.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr17:7574033 C>A did not map to a codon.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr17:61574510 G>A maps to NM_000789.3 G1235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr17:61574510 G>A maps to NM_000789.3 G1235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr19:8321560 G>A maps to NM_024552.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr19:8321560 G>A maps to NM_024552.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr19:10745692 C>T maps to NM_020428.3 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr19:10745692 C>T maps to NM_020428.3 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr19:56539107 C>T maps to NM_153447.4 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr19:56539107 C>T maps to NM_153447.4 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr2:51255024 G>A maps to ENST00000404971 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr2:51255024 G>A maps to ENST00000404971 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr2:98744736 T>A maps to NM_144992.4 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr2:98744736 T>A maps to NM_144992.4 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr2:177036314 G>A maps to NM_006898.4 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr2:177036314 G>A maps to NM_006898.4 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr5:150928975 G>A maps to NM_001447.2 Q1557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr5:150928975 G>A maps to NM_001447.2 Q1557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr6:80197507 C>T maps to NM_181714.3 W436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr6:80197507 C>T maps to NM_181714.3 W436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr8:20074762 A>G maps to NM_001693.3 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr8:20074762 A>G maps to NM_001693.3 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr8:100286453 T>G maps to NM_017890.3 T848T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr8:100286453 T>G maps to NM_017890.3 T848T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr8:144809797 G>A maps to NM_198488.3 D611D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HD-7917-01A-11D-2229-08 chr8:144809797 G>A maps to NM_198488.3 D611D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:6267453 G>A maps to NM_207396.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:6267453 G>A maps to NM_207396.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:11736194 G>C maps to ENST00000376669 S125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:11736194 G>C maps to ENST00000376669 S125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:11983376 G>A maps to ENST00000376576 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:11983376 G>A maps to ENST00000376576 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:16269652 G>T maps to ENST00000375733 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:16269652 G>T maps to ENST00000375733 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:19559126 C>T maps to NM_015047.1 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:19559126 C>T maps to NM_015047.1 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:20915547 C>G did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:20915547 C>G did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:22175512 C>G maps to NM_005529.5 S2486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:22175512 C>G maps to NM_005529.5 S2486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:28599969 G>A maps to NM_031459.3 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:28599969 G>A maps to NM_031459.3 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:32206007 C>T maps to NM_001703.2 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:32206007 C>T maps to NM_001703.2 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:32257954 C>T maps to NM_144569.4 Q941Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:32257954 C>T maps to NM_144569.4 Q941Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:32660618 G>C maps to NM_175852.3 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:32660618 G>C maps to NM_175852.3 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:43895743 C>T maps to NM_015284.2 F558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:43895743 C>T maps to NM_015284.2 F558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:89523837 G>C maps to NM_002053.2 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:89523837 G>C maps to NM_002053.2 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:100551110 C>T maps to NM_194292.1 Q616Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:100551110 C>T maps to NM_194292.1 Q616Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:107599826 G>T maps to NM_018137.2 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:107599826 G>T maps to NM_018137.2 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:117659367 C>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:117659367 C>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:145562414 C>T maps to NM_144698.3 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:145562414 C>T maps to NM_144698.3 L701L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:154223769 G>A maps to NM_014847.3 K489K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:154223769 G>A maps to NM_014847.3 K489K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:154561028 G>A maps to ENST00000292205 I1004I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:154561028 G>A maps to ENST00000292205 I1004I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:155145306 C>T maps to NM_173852.3 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:155145306 C>T maps to NM_173852.3 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:159410405 G>A maps to NM_012351.2 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:159410405 G>A maps to NM_012351.2 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:160093058 C>G maps to NM_000702.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:160093058 C>G maps to NM_000702.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:160181450 C>T maps to ENST00000368075 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:160181450 C>T maps to ENST00000368075 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:167097472 G>A maps to NM_001080426.1 E1035E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:167097472 G>A maps to NM_001080426.1 E1035E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:181058847 C>T maps to NM_016545.4 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:181058847 C>T maps to NM_016545.4 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:183907895 C>T maps to NM_015101.2 *627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:183907895 C>T maps to NM_015101.2 *627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:186089236 G>A maps to NM_031935.2 P4063P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:186089236 G>A maps to NM_031935.2 P4063P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:220936310 G>A maps to NM_017898.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:220936310 G>A maps to NM_017898.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:230473019 C>T maps to ENST00000321327 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:230473019 C>T maps to ENST00000321327 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:230492801 G>A maps to ENST00000321327 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:230492801 G>A maps to ENST00000321327 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:233105695 C>T maps to NM_032324.1 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:233105695 C>T maps to NM_032324.1 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:233105722 C>T maps to NM_032324.1 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:233105722 C>T maps to NM_032324.1 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:237814788 G>A maps to NM_001035.2 K2604K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:237814788 G>A maps to NM_001035.2 K2604K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:247040555 C>T maps to ENST00000428671 L941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:247040555 C>T maps to ENST00000428671 L941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:247614690 C>T maps to NM_001004492.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr1:247614690 C>T maps to NM_001004492.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:7217982 C>T maps to NM_001018039.1 E651E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:7217982 C>T maps to NM_001018039.1 E651E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:7684024 G>C maps to ENST00000256861 S55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:7684024 G>C maps to ENST00000256861 S55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:25887023 C>T maps to NM_020752.2 H823H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:25887023 C>T maps to NM_020752.2 H823H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:34408650 C>T maps to NM_019619.3 A1189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:34408650 C>T maps to NM_019619.3 A1189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:55663094 C>A maps to NM_001142763.1 E1142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:55663094 C>A maps to NM_001142763.1 E1142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:86259713 G>A maps to NM_018999.2 Q803Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:86259713 G>A maps to NM_018999.2 Q803Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:99205727 C>T maps to NM_016046.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:99205727 C>T maps to NM_016046.3 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:102568883 C>G maps to NM_003987.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:102568883 C>G maps to NM_003987.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:115364391 C>T maps to ENST00000369358 K1409K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:115364391 C>T maps to ENST00000369358 K1409K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:115372034 C>T maps to ENST00000369358 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:115372034 C>T maps to ENST00000369358 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:116059061 C>G maps to NM_001001936.1 R690R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:116059061 C>G maps to NM_001001936.1 R690R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:116620557 C>T maps to NM_020940.3 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:116620557 C>T maps to NM_020940.3 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:124050610 G>A maps to ENST00000368994 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:124050610 G>A maps to ENST00000368994 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:812801 C>G maps to NM_001004.3 S105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:812801 C>G maps to NM_001004.3 S105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:4616128 C>T maps to ENST00000450052 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:4616128 C>T maps to ENST00000450052 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:6898069 C>T maps to NM_207186.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:6898069 C>T maps to NM_207186.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:7846616 C>T maps to NM_153445.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:7846616 C>T maps to NM_153445.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:7846841 C>T maps to NM_153445.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:7846841 C>T maps to NM_153445.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:64510275 G>A maps to ENST00000320253 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:64510275 G>A maps to ENST00000320253 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:65486585 C>G maps to NM_182710.1 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:65486585 C>G maps to NM_182710.1 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:67209949 C>A maps to NM_020441.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:67209949 C>A maps to NM_020441.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:67395431 C>T maps to ENST00000376693 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:67395431 C>T maps to ENST00000376693 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:71510691 G>A maps to NM_018172.2 *166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:71510691 G>A maps to NM_018172.2 *166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:73795938 C>T maps to ENST00000334126 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr11:73795938 C>T maps to ENST00000334126 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:2797905 G>A maps to NM_199460.2 G2109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:2797905 G>A maps to NM_199460.2 G2109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:6457039 C>G maps to NM_001159576.1 *729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:6457039 C>G maps to NM_001159576.1 *729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:7177492 G>A maps to NM_001734.3 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:7177492 G>A maps to NM_001734.3 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:21998611 G>A maps to NM_005691.2 V1007V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:21998611 G>A maps to NM_005691.2 V1007V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:31253967 G>C maps to NM_030653.3 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:31253967 G>C maps to NM_030653.3 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:31545219 G>C maps to NM_144973.3 V1149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:31545219 G>C maps to NM_144973.3 V1149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:52314579 G>A maps to NM_001077401.1 W472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:52314579 G>A maps to NM_001077401.1 W472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:52799719 C>T maps to NM_033033.3 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:52799719 C>T maps to NM_033033.3 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:54379123 G>A maps to NM_017409.3 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:54379123 G>A maps to NM_017409.3 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:54383228 G>C maps to NM_017409.3 *343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:54383228 G>C maps to NM_017409.3 *343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:58220808 G>A maps to NM_005730.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:58220808 G>A maps to NM_005730.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:95676360 G>A maps to NM_017599.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:95676360 G>A maps to NM_017599.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:109678959 C>G maps to NM_001093.3 V1632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:109678959 C>G maps to NM_001093.3 V1632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:109685463 G>A maps to NM_001093.3 L1875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:109685463 G>A maps to NM_001093.3 L1875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:112579999 G>T maps to NM_006700.2 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:112579999 G>T maps to NM_006700.2 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:130648350 C>A maps to NM_007197.3 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr12:130648350 C>A maps to NM_007197.3 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr13:25376517 G>C did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr13:25376517 G>C did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr13:49281696 C>T maps to NM_020377.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr13:49281696 C>T maps to NM_020377.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr13:100193036 C>T maps to NM_004800.1 Q300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr13:100193036 C>T maps to NM_004800.1 Q300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr13:113760172 C>T maps to NM_000131.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr13:113760172 C>T maps to NM_000131.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:20844027 C>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:20844027 C>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:21058669 C>T maps to NM_001024822.2 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:21058669 C>T maps to NM_001024822.2 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:38678891 C>T maps to NM_001049.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:38678891 C>T maps to NM_001049.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:39796070 C>G maps to ENST00000396158 S564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:39796070 C>G maps to ENST00000396158 S564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:51381451 G>C maps to NM_002863.4 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:51381451 G>C maps to NM_002863.4 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:76621146 G>A maps to NM_017926.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:76621146 G>A maps to NM_017926.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:88452836 G>A maps to NM_000153.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:88452836 G>A maps to NM_000153.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:93179216 C>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:93179216 C>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:93273115 C>T maps to NM_005113.2 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:93273115 C>T maps to NM_005113.2 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:101200977 C>T maps to NM_003836.5 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:101200977 C>T maps to NM_003836.5 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:102505825 G>A maps to NM_001376.4 L3846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:102505825 G>A maps to NM_001376.4 L3846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:104205237 C>T maps to NM_015316.2 Q905Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:104205237 C>T maps to NM_015316.2 Q905Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:105410276 C>G maps to NM_138420.2 V3837V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:105410276 C>G maps to NM_138420.2 V3837V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:105411032 C>G maps to NM_138420.2 L3585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr14:105411032 C>G maps to NM_138420.2 L3585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr15:22933612 C>T maps to NM_014608.2 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr15:22933612 C>T maps to NM_014608.2 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr15:40068690 G>C maps to NM_152597.4 S12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr15:40068690 G>C maps to NM_152597.4 S12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr15:43022881 C>T maps to NM_138477.2 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr15:43022881 C>T maps to NM_138477.2 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr15:90801268 G>A did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr15:90801268 G>A did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr15:91795214 C>T maps to NM_014848.4 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr15:91795214 C>T maps to NM_014848.4 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:819430 G>C maps to NM_001025190.1 L1053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:819430 G>C maps to NM_001025190.1 L1053L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:1962145 G>A maps to ENST00000454677 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:1962145 G>A maps to ENST00000454677 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:2228625 G>A maps to NM_020764.3 S1407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:2228625 G>A maps to NM_020764.3 S1407S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HL-7533-01A-11D-2229-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:2580408 G>T maps to NM_001145815.1 V478V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HL-7533-01A-11D-2229-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:2580408 G>T maps to NM_001145815.1 V478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:3614247 G>A maps to ENST00000448023 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:3614247 G>A maps to ENST00000448023 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:4944532 C>T maps to NM_002705.4 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:4944532 C>T maps to NM_002705.4 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:9892209 A>C maps to NM_000833.3 G760G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:9892209 A>C maps to NM_000833.3 G760G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:20451747 G>C maps to NM_017888.2 *580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:20451747 G>C maps to NM_017888.2 *580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:48596193 G>A maps to NM_153029.3 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:48596193 G>A maps to NM_153029.3 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:53513067 C>T maps to NM_005611.3 V902V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:53513067 C>T maps to NM_005611.3 V902V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:58032105 G>A maps to NM_020807.1 Q22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:58032105 G>A maps to NM_020807.1 Q22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:67237257 G>A maps to NM_024712.3 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:67237257 G>A maps to NM_024712.3 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:67915423 C>T maps to NM_014329.3 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:67915423 C>T maps to NM_014329.3 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:83948559 G>C did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:83948559 G>C did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:89977644 G>C maps to NM_014972.2 *677S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr16:89977644 G>C maps to NM_014972.2 *677S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HL-7533-01A-11D-2229-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-HL-7533-01A-11D-2229-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:1478936 G>C maps to ENST00000382147 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:1478936 G>C maps to ENST00000382147 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:3119394 C>T maps to NM_014565.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:3119394 C>T maps to NM_014565.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:7144690 G>A maps to NM_007278.1 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:7144690 G>A maps to NM_007278.1 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:7417450 C>T maps to NM_000937.4 L1956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:7417450 C>T maps to NM_000937.4 L1956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:8192665 G>C maps to NM_016492.4 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:8192665 G>C maps to NM_016492.4 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:16455378 G>A maps to NM_020653.2 Q693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:16455378 G>A maps to NM_020653.2 Q693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:29226354 G>A maps to NM_024683.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:29226354 G>A maps to NM_024683.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:33318805 G>A maps to NM_013975.3 K386K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:33318805 G>A maps to NM_013975.3 K386K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:34050651 G>A maps to NM_001030006.1 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:34050651 G>A maps to NM_001030006.1 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:42287533 C>T maps to NM_014233.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:42287533 C>T maps to NM_014233.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:48154039 G>A maps to NM_002204.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:48154039 G>A maps to NM_002204.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:57270938 G>C maps to NM_018304.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:57270938 G>C maps to NM_018304.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:61902703 G>A maps to NM_017647.3 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:61902703 G>A maps to NM_017647.3 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:72768369 C>G maps to NM_015654.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:72768369 C>G maps to NM_015654.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:73038631 G>C maps to NM_006356.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:73038631 G>C maps to NM_006356.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:74902122 G>C maps to NM_198955.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:74902122 G>C maps to NM_198955.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:78357724 G>A maps to NM_020914.4 Q4822Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:78357724 G>A maps to NM_020914.4 Q4822Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:79637312 C>T maps to NM_199287.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:79637312 C>T maps to NM_199287.2 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:80014846 C>T maps to NM_212492.1 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr17:80014846 C>T maps to NM_212492.1 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr18:357514 C>T maps to NM_130386.2 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr18:357514 C>T maps to NM_130386.2 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr18:6978306 C>T maps to NM_005559.2 L2026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr18:6978306 C>T maps to NM_005559.2 L2026L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr18:12028067 G>T maps to NM_014214.1 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr18:12028067 G>T maps to NM_014214.1 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:4345869 G>A maps to ENST00000262967 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:4345869 G>A maps to ENST00000262967 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:5595457 G>A maps to NM_014649.2 I611I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:5595457 G>A maps to NM_014649.2 I611I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:5776272 C>T maps to NM_152784.3 F681F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:5776272 C>T maps to NM_152784.3 F681F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:7529458 G>A maps to NM_001130955.1 K741K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:7529458 G>A maps to NM_001130955.1 K741K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:10206705 G>A maps to NM_031917.2 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:10206705 G>A maps to NM_031917.2 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:14507943 C>T maps to NM_078481.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:14507943 C>T maps to NM_078481.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:14829048 C>T maps to NM_032433.2 Q304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:14829048 C>T maps to NM_032433.2 Q304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:15226871 C>T maps to NM_006844.3 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:15226871 C>T maps to NM_006844.3 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:15350584 C>T maps to NM_058243.2 V1110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:15350584 C>T maps to NM_058243.2 V1110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:38861430 G>C maps to NM_021185.4 *1160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:38861430 G>C maps to NM_021185.4 *1160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:42600012 G>A maps to ENST00000342301 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:42600012 G>A maps to ENST00000342301 F239F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:42795872 G>A maps to NM_015125.3 Q954Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:42795872 G>A maps to NM_015125.3 Q954Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:43031508 G>C maps to NM_001712.4 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:43031508 G>C maps to NM_001712.4 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:44008098 C>A maps to NM_198850.3 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:44008098 C>A maps to NM_198850.3 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:49850455 G>C maps to NM_003598.1 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:49850455 G>C maps to NM_003598.1 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:50204036 G>A maps to NM_152359.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:50204036 G>A maps to NM_152359.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:51274297 C>G maps to NM_001506.1 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr19:51274297 C>G maps to NM_001506.1 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:15470865 G>A maps to NM_015909.2 S1401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:15470865 G>A maps to NM_015909.2 S1401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:39070333 C>G maps to NM_198963.1 G746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:39070333 C>G maps to NM_198963.1 G746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:44586818 C>T maps to NM_001171603.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:44586818 C>T maps to NM_001171603.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:47600695 C>T maps to ENST00000426238 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:47600695 C>T maps to ENST00000426238 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:64147044 C>T maps to NM_016516.2 K712K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:64147044 C>T maps to NM_016516.2 K712K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:74326530 A>C maps to ENST00000409262 A1039A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:74326530 A>C maps to ENST00000409262 A1039A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:86276113 G>A maps to NM_015425.3 R843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:86276113 G>A maps to NM_015425.3 R843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:97427041 C>G maps to NM_020184.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:97427041 C>G maps to NM_020184.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:101011993 G>A maps to NM_004854.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:101011993 G>A maps to NM_004854.3 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:169571585 C>T maps to ENST00000392687 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:169571585 C>T maps to ENST00000392687 R229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:179615717 C>T maps to ENST00000375038 Q3805Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:179615717 C>T maps to ENST00000375038 Q3805Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:219249961 C>T maps to NM_000578.3 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr2:219249961 C>T maps to NM_000578.3 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:5100330 C>T maps to NM_002592.2 Q38Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:5100330 C>T maps to NM_002592.2 Q38Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:33329792 G>A maps to NM_014071.2 Q1423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:33329792 G>A maps to NM_014071.2 Q1423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:33588930 G>A maps to NM_020884.3 G1857G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:33588930 G>A maps to NM_020884.3 G1857G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:34797519 C>T maps to NM_012156.2 F593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:34797519 C>T maps to NM_012156.2 F593F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:44588037 G>A maps to NM_022095.3 F685F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:44588037 G>A maps to NM_022095.3 F685F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:50292703 C>G maps to NM_006045.1 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:50292703 C>G maps to NM_006045.1 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:61512068 G>A maps to NM_033081.2 Q1747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:61512068 G>A maps to NM_033081.2 Q1747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:62200814 G>C maps to NM_001037335.2 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:62200814 G>C maps to NM_001037335.2 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:62340462 G>A maps to NM_032527.4 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr20:62340462 G>A maps to NM_032527.4 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr21:40720241 C>T maps to NM_004965.6 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr21:40720241 C>T maps to NM_004965.6 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:21377814 C>T maps to NM_005446.3 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:21377814 C>T maps to NM_005446.3 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:24939876 G>A maps to ENST00000266155 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:24939876 G>A maps to ENST00000266155 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:38823411 G>A maps to NM_152868.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:38823411 G>A maps to NM_152868.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:38823924 G>C maps to NM_152868.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:38823924 G>C maps to NM_152868.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:50298024 G>A maps to NM_024105.3 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:50298024 G>A maps to NM_024105.3 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:50591517 G>A maps to NM_018995.2 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:50591517 G>A maps to NM_018995.2 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:50728134 T>C maps to NM_012401.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr22:50728134 T>C maps to NM_012401.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:1424825 G>A maps to NM_014461.2 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:1424825 G>A maps to NM_014461.2 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:45636826 G>A maps to NM_014240.2 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:45636826 G>A maps to NM_014240.2 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:56681003 G>A maps to ENST00000447900 F587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:56681003 G>A maps to ENST00000447900 F587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:77089918 C>G did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:77089918 C>G did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:97596631 G>C maps to ENST00000182096 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:97596631 G>C maps to ENST00000182096 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:113440618 C>T maps to NM_025146.2 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:113440618 C>T maps to NM_025146.2 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:115571360 C>T maps to NM_002338.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:115571360 C>T maps to NM_002338.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:119422062 C>T maps to NM_033364.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:119422062 C>T maps to NM_033364.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:133667437 G>C maps to NM_005630.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:133667437 G>C maps to NM_005630.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:135720852 C>T maps to NM_002718.4 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:135720852 C>T maps to NM_002718.4 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:135870600 C>T maps to NM_018133.3 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:135870600 C>T maps to NM_018133.3 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:141163752 G>A maps to NM_001080412.2 V841V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:141163752 G>A maps to NM_001080412.2 V841V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:141205978 G>C maps to ENST00000452898 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:141205978 G>C maps to ENST00000452898 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:142467158 C>T maps to ENST00000476941 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:142467158 C>T maps to ENST00000476941 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:194118044 G>A maps to NM_004488.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr3:194118044 G>A maps to NM_004488.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:3144491 G>C did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:3144491 G>C did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:5528038 C>G maps to NM_005750.2 S88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:5528038 C>G maps to NM_005750.2 S88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:76812834 G>T maps to NM_006239.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:76812834 G>T maps to NM_006239.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:89599158 C>T maps to NM_014606.1 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:89599158 C>T maps to NM_014606.1 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:123813549 G>A maps to NM_002006.4 *289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:123813549 G>A maps to NM_002006.4 *289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:129770158 C>T maps to NM_199320.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:129770158 C>T maps to NM_199320.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:139966177 C>T maps to NM_012118.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:139966177 C>T maps to NM_012118.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:156841120 C>T maps to NM_005651.2 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:156841120 C>T maps to NM_005651.2 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:186536297 C>T maps to ENST00000355634 K985K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:186536297 C>T maps to ENST00000355634 K985K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:187630532 G>C maps to ENST00000260147 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr4:187630532 G>C maps to ENST00000260147 S150*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HL-7533-01A-11D-2229-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-HL-7533-01A-11D-2229-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:112343709 C>T maps to NM_152624.4 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:112343709 C>T maps to NM_152624.4 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:131822132 T>C did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:131822132 T>C did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:134130684 C>G maps to ENST00000452510 S591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:134130684 C>G maps to ENST00000452510 S591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:137802773 G>T maps to NM_001964.2 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:137802773 G>T maps to NM_001964.2 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:137802792 G>T maps to NM_001964.2 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:137802792 G>T maps to NM_001964.2 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:140215184 C>A maps to NM_018910.2 S406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:140215184 C>A maps to NM_018910.2 S406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:147803612 G>A maps to NM_205836.1 E557E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:147803612 G>A maps to NM_205836.1 E557E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:149589168 G>C maps to NM_014228.3 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:149589168 G>C maps to NM_014228.3 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:149602273 C>G maps to NM_015981.3 *490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:149602273 C>G maps to NM_015981.3 *490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:151231079 G>A maps to NM_001146040.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:151231079 G>A maps to NM_001146040.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:154188022 G>A maps to ENST00000377643 R901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:154188022 G>A maps to ENST00000377643 R901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:169125438 C>T maps to NM_004946.2 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:169125438 C>T maps to NM_004946.2 F347F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:176306885 G>A maps to NM_133369.2 *843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:176306885 G>A maps to NM_133369.2 *843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:176314713 G>C maps to NM_002115.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:176314713 G>C maps to NM_002115.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:179740937 G>A maps to NM_005110.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr5:179740937 G>A maps to NM_005110.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:7574982 C>G maps to NM_004415.2 V797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:7574982 C>G maps to NM_004415.2 V797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:24718800 G>A maps to NM_030939.4 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:24718800 G>A maps to NM_030939.4 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:26017360 C>A maps to NM_005325.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:26017360 C>A maps to NM_005325.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:28542878 G>A maps to NM_052923.1 Q535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:28542878 G>A maps to NM_052923.1 Q535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:29408427 C>T maps to NM_013941.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:29408427 C>T maps to NM_013941.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:29911303 G>A maps to ENST00000376806 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:29911303 G>A maps to ENST00000376806 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:30863239 C>T maps to NM_013994.2 R525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:30863239 C>T maps to NM_013994.2 R525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:31833470 G>A maps to NM_025257.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:31833470 G>A maps to NM_025257.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:32166500 C>T maps to NM_004557.3 L1514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:32166500 C>T maps to NM_004557.3 L1514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:36508035 G>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:36508035 G>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:38816450 C>T maps to ENST00000327475 I1679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:38816450 C>T maps to ENST00000327475 I1679I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:52767199 G>A maps to NM_000847.4 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:52767199 G>A maps to NM_000847.4 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:90364053 C>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:90364053 C>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:146350787 C>T maps to NM_000838.3 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:146350787 C>T maps to NM_000838.3 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:152708395 C>T maps to NM_182961.2 L2766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr6:152708395 C>T maps to NM_182961.2 L2766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:4089059 C>T maps to NM_152744.3 Q895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:4089059 C>T maps to NM_152744.3 Q895*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:20199824 G>A maps to NM_182762.3 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:20199824 G>A maps to NM_182762.3 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:64167168 G>T maps to NM_016220.3 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:64167168 G>T maps to NM_016220.3 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:91622236 A>G maps to NM_005751.4 Q148Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:91622236 A>G maps to NM_005751.4 Q148Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:98457824 G>A maps to NM_001134450.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:98457824 G>A maps to NM_001134450.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:107204317 G>A maps to NM_006348.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:107204317 G>A maps to NM_006348.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:117431593 G>A maps to NM_033427.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:117431593 G>A maps to NM_033427.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:136938250 C>T maps to NM_002825.5 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:136938250 C>T maps to NM_002825.5 Q83Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:141763321 C>T maps to ENST00000475668 F1427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:141763321 C>T maps to ENST00000475668 F1427F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:158557394 G>A maps to NM_020728.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr7:158557394 G>A maps to NM_020728.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr8:71520407 C>T maps to NM_014294.5 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr8:71520407 C>T maps to NM_014294.5 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr8:130760898 C>A maps to NM_031415.2 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr8:130760898 C>A maps to NM_031415.2 E459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr8:142238342 G>C maps to NM_001080431.1 S8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr8:142238342 G>C maps to NM_001080431.1 S8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr8:144943050 G>A maps to NM_031308.1 V1457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr8:144943050 G>A maps to NM_031308.1 V1457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:117880 G>C maps to NM_207305.3 S80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:117880 G>C maps to NM_207305.3 S80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:14797545 G>A maps to ENST00000380880 T1266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:14797545 G>A maps to ENST00000380880 T1266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:21818160 C>T maps to NM_002451.3 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:21818160 C>T maps to NM_002451.3 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:37592508 G>C maps to NM_001134485.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:37592508 G>C maps to NM_001134485.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:91652994 C>T maps to NM_016848.5 K523K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:91652994 C>T maps to NM_016848.5 K523K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:135447845 G>A maps to NM_207417.1 E304E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:135447845 G>A maps to NM_207417.1 E304E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:140330689 G>A maps to NM_001033113.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr9:140330689 G>A maps to NM_001033113.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chrX:32404564 C>G maps to ENST00000357033 L1512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chrX:32404564 C>G maps to ENST00000357033 L1512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chrX:151336901 G>C maps to NM_000808.3 S426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chrX:151336901 G>C maps to NM_000808.3 S426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr1:22191362 C>T maps to NM_005529.5 P1533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr1:22191362 C>T maps to NM_005529.5 P1533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr1:47689751 C>T maps to ENST00000371883 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr1:47689751 C>T maps to ENST00000371883 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr1:59002203 G>T maps to NM_145243.3 S237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr1:59002203 G>T maps to NM_145243.3 S237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr1:197889130 C>T maps to NM_020204.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr1:197889130 C>T maps to NM_020204.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr1:200017720 G>T maps to NM_205860.1 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr1:200017720 G>T maps to NM_205860.1 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr10:115804436 G>A maps to NM_000684.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr10:115804436 G>A maps to NM_000684.2 V182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr11:71721848 G>A maps to ENST00000393695 Q1574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr11:71721848 G>A maps to ENST00000393695 Q1574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr12:53450796 G>A maps to NM_170754.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr12:53450796 G>A maps to NM_170754.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr12:54576248 G>A maps to NM_014311.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr12:54576248 G>A maps to NM_014311.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr13:99378414 G>A maps to NM_005073.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr13:99378414 G>A maps to NM_005073.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr14:64565539 G>A did not map to a codon.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr14:64565539 G>A did not map to a codon.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr14:74345929 C>A maps to NM_152444.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr14:74345929 C>A maps to NM_152444.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr14:92347670 G>A maps to ENST00000267620 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr14:92347670 G>A maps to ENST00000267620 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr14:99182521 C>T did not map to a codon.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr14:99182521 C>T did not map to a codon.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr14:105518368 G>A maps to NM_013345.2 N35N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr14:105518368 G>A maps to NM_013345.2 N35N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr15:52664413 G>C maps to ENST00000358212 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr15:52664413 G>C maps to ENST00000358212 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr15:65555625 G>A maps to NM_017851.4 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr15:65555625 G>A maps to NM_017851.4 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr16:67979116 T>C maps to NM_005072.4 Q1013Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr16:67979116 T>C maps to NM_005072.4 Q1013Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr17:7800528 G>A maps to NM_001005271.2 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr17:7800528 G>A maps to NM_001005271.2 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr17:62080238 C>T maps to NM_001099789.1 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr17:62080238 C>T maps to NM_001099789.1 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr19:2210645 G>A maps to ENST00000221482 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr19:2210645 G>A maps to ENST00000221482 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr19:10124178 C>T maps to NM_015725.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr19:10124178 C>T maps to NM_015725.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr19:39521761 C>T maps to NM_178820.3 W160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr19:39521761 C>T maps to NM_178820.3 W160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr19:39905660 C>T maps to NM_022835.2 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr19:39905660 C>T maps to NM_022835.2 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr19:47823720 G>A maps to ENST00000355085 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr19:47823720 G>A maps to ENST00000355085 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr19:50461906 G>A maps to NM_052884.2 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr19:50461906 G>A maps to NM_052884.2 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr2:33036233 G>A maps to NM_017735.4 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr2:33036233 G>A maps to NM_017735.4 L714L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr2:71755437 C>T maps to NM_001130987.1 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr2:71755437 C>T maps to NM_001130987.1 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr2:99013651 G>T maps to NM_001298.2 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr2:99013651 G>T maps to NM_001298.2 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr2:228563677 G>A maps to NM_025243.3 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr2:228563677 G>A maps to NM_025243.3 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr20:9510394 C>T maps to NM_012261.3 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr20:9510394 C>T maps to NM_012261.3 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr22:30061030 C>G maps to NM_181832.2 S288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr22:30061030 C>G maps to NM_181832.2 S288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr3:37523000 C>T maps to NM_002207.2 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr3:37523000 C>T maps to NM_002207.2 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr3:58395288 C>T maps to NM_017771.3 Q447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr3:58395288 C>T maps to NM_017771.3 Q447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr3:58516344 G>A maps to NM_003500.3 Y280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr3:58516344 G>A maps to NM_003500.3 Y280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr3:169801876 T>C maps to NM_014373.2 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr3:169801876 T>C maps to NM_014373.2 N39N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr4:22820362 C>G maps to NM_020973.3 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr4:22820362 C>G maps to NM_020973.3 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr4:37848659 G>A maps to NM_018290.3 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr4:37848659 G>A maps to NM_018290.3 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr5:140216299 C>T maps to NM_018910.2 Q778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr5:140216299 C>T maps to NM_018910.2 Q778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr6:38825333 C>G maps to ENST00000327475 S1913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr6:38825333 C>G maps to ENST00000327475 S1913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr6:105606598 G>A maps to NM_022361.4 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr6:105606598 G>A maps to NM_022361.4 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr7:100391589 G>A maps to ENST00000349350 Q2645Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr7:100391589 G>A maps to ENST00000349350 Q2645Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr7:101840037 C>T maps to ENST00000360264 H460H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr7:101840037 C>T maps to ENST00000360264 H460H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr7:119915561 C>T maps to NM_012281.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr7:119915561 C>T maps to NM_012281.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr7:127255553 G>C maps to NM_006193.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr7:127255553 G>C maps to NM_006193.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr7:149430328 G>A maps to NM_032534.2 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr7:149430328 G>A maps to NM_032534.2 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr8:61178600 C>T maps to NM_004056.4 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr8:61178600 C>T maps to NM_004056.4 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr9:35377546 C>T maps to ENST00000396787 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr9:35377546 C>T maps to ENST00000396787 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr9:35724887 C>T maps to NM_006289.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chr9:35724887 C>T maps to NM_006289.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chrX:120008978 T>C maps to NM_001145718.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7630-01A-11D-2078-08 chrX:120008978 T>C maps to NM_001145718.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr1:7812555 C>T maps to NM_015215.2 R1641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr1:7812555 C>T maps to NM_015215.2 R1641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr1:33236051 C>T maps to NM_020888.2 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr1:33236051 C>T maps to NM_020888.2 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr1:217955574 G>A maps to NM_138796.2 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr1:217955574 G>A maps to NM_138796.2 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr1:227968340 C>T maps to NM_053052.3 D454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr1:227968340 C>T maps to NM_053052.3 D454D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr19:55396848 C>T maps to NM_002000.2 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr19:55396848 C>T maps to NM_002000.2 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr2:24111243 A>G maps to NM_017552.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr2:24111243 A>G maps to NM_017552.1 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr2:74746712 C>T maps to NM_133637.2 Q592Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr2:74746712 C>T maps to NM_133637.2 Q592Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr20:31571671 G>A maps to NM_080675.3 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr20:31571671 G>A maps to NM_080675.3 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr4:25363859 G>A maps to NM_024936.2 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr4:25363859 G>A maps to NM_024936.2 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr5:179765550 G>T maps to NM_005110.2 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr5:179765550 G>T maps to NM_005110.2 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr6:31930805 C>T maps to NM_006929.4 H447H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr6:31930805 C>T maps to NM_006929.4 H447H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr7:63680364 C>G maps to NM_001159524.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr7:63680364 C>G maps to NM_001159524.1 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr7:146741039 C>T maps to NM_014141.5 H148H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr7:146741039 C>T maps to NM_014141.5 H148H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr7:149545304 A>C maps to NM_001099220.1 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr7:149545304 A>C maps to NM_001099220.1 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr8:12950233 G>A maps to NM_182643.2 S1209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr8:12950233 G>A maps to NM_182643.2 S1209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr8:144652141 C>T maps to NM_001100878.1 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr8:144652141 C>T maps to NM_001100878.1 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr9:91041468 C>T maps to NM_006717.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7631-01A-11D-2078-08 chr9:91041468 C>T maps to NM_006717.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr1:117624535 A>T maps to NM_003594.3 K624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr1:117624535 A>T maps to NM_003594.3 K624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr1:169390948 A>C maps to ENST00000367806 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr1:169390948 A>C maps to ENST00000367806 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr1:206628235 C>T maps to ENST00000414359 V714V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr1:206628235 C>T maps to ENST00000414359 V714V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr10:63450357 A>G maps to NM_173554.2 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr10:63450357 A>G maps to NM_173554.2 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr12:49445625 C>A maps to NM_003482.3 E614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr12:49445625 C>A maps to NM_003482.3 E614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr12:57958725 C>T maps to NM_004984.2 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr12:57958725 C>T maps to NM_004984.2 H157H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr12:72070611 G>A maps to NM_031435.3 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr12:72070611 G>A maps to NM_031435.3 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr15:82444534 G>A maps to NM_024580.5 R754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr15:82444534 G>A maps to NM_024580.5 R754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr15:85447423 C>T maps to NM_004213.3 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr15:85447423 C>T maps to NM_004213.3 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr16:72828432 G>A maps to NM_006885.3 C2716C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr16:72828432 G>A maps to NM_006885.3 C2716C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr18:13645526 C>T maps to NM_181481.3 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr18:13645526 C>T maps to NM_181481.3 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr19:38102813 T>C maps to NM_152606.3 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr19:38102813 T>C maps to NM_152606.3 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr20:30897726 G>A maps to NM_004798.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr20:30897726 G>A maps to NM_004798.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr22:32548590 C>T maps to NM_001010859.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr22:32548590 C>T maps to NM_001010859.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr4:72412191 G>A maps to NM_001098484.2 K856K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr4:72412191 G>A maps to NM_001098484.2 K856K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr5:176951738 G>A maps to ENST00000442143 N661N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr5:176951738 G>A maps to ENST00000442143 N661N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr6:30888895 C>T maps to NM_001167734.1 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr6:30888895 C>T maps to NM_001167734.1 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr6:31832498 C>A maps to NM_025257.2 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr6:31832498 C>A maps to NM_025257.2 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr6:38840790 C>T maps to ENST00000327475 R2437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr6:38840790 C>T maps to ENST00000327475 R2437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr6:96971058 T>C maps to NM_015323.4 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IQ-7632-01A-11D-2078-08 chr6:96971058 T>C maps to NM_015323.4 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:179583700 C>G did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:179583700 C>G did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:179659843 G>T maps to NM_133378.4 Y350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr2:179659843 G>T maps to NM_133378.4 Y350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr8:110346584 G>C did not map to a codon.
Sequencing variant TCGA-BA-4076-01A-01D-1434-08 chr8:110346584 G>C did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:124670354 C>T did not map to a codon.
Sequencing variant TCGA-BA-4078-01A-01D-1434-08 chr11:124670354 C>T did not map to a codon.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr21:11014972 T>C did not map to a codon.
Sequencing variant TCGA-BA-5149-01A-01D-1512-08 chr21:11014972 T>C did not map to a codon.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr8:110346613 G>A did not map to a codon.
Sequencing variant TCGA-BA-5151-01A-01D-1434-08 chr8:110346613 G>A did not map to a codon.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:46977337 C>T maps to ENST00000283297 W612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5152-01A-02D-1870-08 chr6:46977337 C>T maps to ENST00000283297 W612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:12979809 C>T maps to NM_001012277.1 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:12979809 C>T maps to NM_001012277.1 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:90459558 C>T did not map to a codon.
Sequencing variant TCGA-BA-5558-01A-01D-1512-08 chr1:90459558 C>T did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:206856278 C>G did not map to a codon.
Sequencing variant TCGA-BB-4223-01A-01D-1434-08 chr1:206856278 C>G did not map to a codon.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr16:202961 C>T maps to NM_005332.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-4227-01A-01D-1870-08 chr16:202961 C>T maps to NM_005332.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:201195237 C>A maps to NM_001164586.1 I3591I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr1:201195237 C>A maps to NM_001164586.1 I3591I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr8:26238680 A>T did not map to a codon.
Sequencing variant TCGA-BB-7862-01A-21D-2229-08 chr8:26238680 A>T did not map to a codon.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr9:131873255 A>C did not map to a codon.
Sequencing variant TCGA-BB-7866-01A-11D-2229-08 chr9:131873255 A>C did not map to a codon.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:26671806 G>A maps to NM_001039775.3 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr1:26671806 G>A maps to NM_001039775.3 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:113147641 C>G maps to NM_005054.2 V960V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BB-7871-01A-11D-2229-08 chr2:113147641 C>G maps to NM_005054.2 V960V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:100660969 C>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr12:100660969 C>A did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:96000109 C>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr14:96000109 C>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:39897485 C>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:39897485 C>T did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:47151759 G>C maps to NM_145056.2 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr19:47151759 G>C maps to NM_145056.2 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:219127710 C>G maps to NM_170699.2 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr2:219127710 C>G maps to NM_170699.2 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:26238783 C>G did not map to a codon.
Sequencing variant TCGA-CN-4723-01A-01D-1434-08 chr8:26238783 C>G did not map to a codon.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:176707724 G>T maps to NM_022455.4 G1928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4727-01A-01D-1434-08 chr5:176707724 G>T maps to NM_022455.4 G1928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr7:128696594 G>A did not map to a codon.
Sequencing variant TCGA-CN-4729-01A-01D-1434-08 chr7:128696594 G>A did not map to a codon.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:235324585 A>G maps to ENST00000474953 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr1:235324585 A>G maps to ENST00000474953 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr12:28410060 A>G did not map to a codon.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr12:28410060 A>G did not map to a codon.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr17:7579590 C>T did not map to a codon.
Sequencing variant TCGA-CN-4740-01A-01D-1434-08 chr17:7579590 C>T did not map to a codon.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:13080365 G>C did not map to a codon.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr19:13080365 G>C did not map to a codon.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr6:170151654 G>T did not map to a codon.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr6:170151654 G>T did not map to a codon.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr8:33371070 G>C did not map to a codon.
Sequencing variant TCGA-CN-4741-01A-01D-1434-08 chr8:33371070 G>C did not map to a codon.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr6:168226810 T>C did not map to a codon.
Sequencing variant TCGA-CN-4742-01A-02D-1512-08 chr6:168226810 T>C did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:8008810 T>C did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr11:8008810 T>C did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr21:10998290 C>A did not map to a codon.
Sequencing variant TCGA-CN-5360-01A-01D-1434-08 chr21:10998290 C>A did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr3:93782066 T>G did not map to a codon.
Sequencing variant TCGA-CN-5363-01A-01D-1434-08 chr3:93782066 T>G did not map to a codon.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:26672989 C>T maps to NM_001039775.3 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5364-01A-01D-1434-08 chr1:26672989 C>T maps to NM_001039775.3 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:90459792 G>C did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr1:90459792 G>C did not map to a codon.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:65370406 C>T maps to NM_001101362.2 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5369-01A-01D-1434-08 chr15:65370406 C>T maps to NM_001101362.2 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr4:189026442 C>T did not map to a codon.
Sequencing variant TCGA-CN-5374-01A-01D-1434-08 chr4:189026442 C>T did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:571570 C>T maps to NM_198591.1 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:571570 C>T maps to NM_198591.1 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:47151924 G>A maps to NM_145056.2 D568D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr19:47151924 G>A maps to NM_145056.2 D568D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr4:169393961 T>C did not map to a codon.
Sequencing variant TCGA-CN-6011-01A-11D-1683-08 chr4:169393961 T>C did not map to a codon.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr1:2985741 C>G did not map to a codon.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr1:2985741 C>G did not map to a codon.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr6:151936745 G>T maps to ENST00000367290 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chr6:151936745 G>T maps to ENST00000367290 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chrX:24332221 C>G did not map to a codon.
Sequencing variant TCGA-CN-6012-01A-11D-1683-08 chrX:24332221 C>G did not map to a codon.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:193029107 C>T maps to ENST00000417752 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr1:193029107 C>T maps to ENST00000417752 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr6:66204796 C>T maps to ENST00000370616 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6013-01A-11D-1683-08 chr6:66204796 C>T maps to ENST00000370616 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr21:11012948 A>G did not map to a codon.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr21:11012948 A>G did not map to a codon.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr8:145235409 C>T maps to NM_032450.2 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6018-01A-11D-1683-08 chr8:145235409 C>T maps to NM_032450.2 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr11:5153872 G>T did not map to a codon.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr11:5153872 G>T did not map to a codon.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr18:10672763 C>T maps to NM_022068.2 P2643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6020-01A-11D-1683-08 chr18:10672763 C>T maps to NM_022068.2 P2643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr19:53067394 A>T did not map to a codon.
Sequencing variant TCGA-CN-6021-01A-11D-1683-08 chr19:53067394 A>T did not map to a codon.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:60620856 G>C maps to NM_004778.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5326-01A-01D-1870-08 chr11:60620856 G>C maps to NM_004778.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chrX:153640368 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5327-01A-01D-1683-08 chrX:153640368 C>T did not map to a codon.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr16:2031219 G>T did not map to a codon.
Sequencing variant TCGA-CQ-5332-01A-01D-1683-08 chr16:2031219 G>T did not map to a codon.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr1:153520230 G>C maps to NM_002960.1 S78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chr1:153520230 G>C maps to NM_002960.1 S78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chrX:72797281 C>G maps to NM_001039840.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-5334-01A-01D-1683-08 chrX:72797281 C>G maps to NM_001039840.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr1:90459478 C>T did not map to a codon.
Sequencing variant TCGA-CQ-6219-01A-11D-1912-08 chr1:90459478 C>T did not map to a codon.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr1:45271806 C>T maps to NM_001013632.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6224-01A-11D-1912-08 chr1:45271806 C>T maps to NM_001013632.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr13:78493511 C>T did not map to a codon.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr13:78493511 C>T did not map to a codon.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr5:140529802 A>C did not map to a codon.
Sequencing variant TCGA-CQ-6228-01A-11D-1912-08 chr5:140529802 A>C did not map to a codon.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr17:14140167 C>A did not map to a codon.
Sequencing variant TCGA-CQ-7067-01A-11D-2229-08 chr17:14140167 C>A did not map to a codon.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr1:26671978 A>T maps to NM_001039775.3 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5243-01A-01D-1512-08 chr1:26671978 A>T maps to NM_001039775.3 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr6:168226204 G>A did not map to a codon.
Sequencing variant TCGA-CR-5248-01A-01D-2012-08 chr6:168226204 G>A did not map to a codon.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr19:53367198 G>A did not map to a codon.
Sequencing variant TCGA-CR-5249-01A-01D-1512-08 chr19:53367198 G>A did not map to a codon.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr10:17875800 G>A maps to NM_002438.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6471-01A-11D-1870-08 chr10:17875800 G>A maps to NM_002438.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:55668993 G>C did not map to a codon.
Sequencing variant TCGA-CR-6472-01A-11D-1870-08 chr19:55668993 G>C did not map to a codon.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr2:97543731 C>T maps to ENST00000417561 T782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6473-01A-11D-1870-08 chr2:97543731 C>T maps to ENST00000417561 T782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr19:12807410 G>A did not map to a codon.
Sequencing variant TCGA-CR-6480-01A-11D-1870-08 chr19:12807410 G>A did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:160958211 C>T did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr2:160958211 C>T did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:66204658 A>G maps to ENST00000370616 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr6:66204658 A>G maps to ENST00000370616 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:124413316 G>A did not map to a codon.
Sequencing variant TCGA-CR-6481-01A-11D-1870-08 chr8:124413316 G>A did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr13:24471142 G>A did not map to a codon.
Sequencing variant TCGA-CR-6484-01A-11D-1870-08 chr13:24471142 G>A did not map to a codon.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr12:49448692 G>A maps to NM_003482.3 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr12:49448692 G>A maps to NM_003482.3 Q56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr5:140165874 A>G did not map to a codon.
Sequencing variant TCGA-CR-6487-01A-11D-1870-08 chr5:140165874 A>G did not map to a codon.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr1:171621792 G>A did not map to a codon.
Sequencing variant TCGA-CR-6491-01A-11D-1870-08 chr1:171621792 G>A did not map to a codon.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr4:187542659 G>A maps to ENST00000260147 Q1697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-6492-01A-12D-2078-08 chr4:187542659 G>A maps to ENST00000260147 Q1697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:5757696 T>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr11:5757696 T>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr12:57881757 G>T did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr12:57881757 G>T did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr22:21333754 C>T did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr22:21333754 C>T did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr3:134070859 G>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr3:134070859 G>A did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:70080466 C>T did not map to a codon.
Sequencing variant TCGA-CR-7364-01A-11D-2012-08 chr4:70080466 C>T did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:53122256 A>T did not map to a codon.
Sequencing variant TCGA-CR-7370-01A-11D-2129-08 chr19:53122256 A>T did not map to a codon.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chrX:25033719 T>A maps to NM_139058.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7371-01A-11D-2012-08 chrX:25033719 T>A maps to NM_139058.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr17:78388915 C>G did not map to a codon.
Sequencing variant TCGA-CR-7374-01A-11D-2012-08 chr17:78388915 C>G did not map to a codon.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr8:91929770 A>T maps to NM_022351.4 K137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7379-01A-11D-2012-08 chr8:91929770 A>T maps to NM_022351.4 K137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr19:51506323 C>T did not map to a codon.
Sequencing variant TCGA-CR-7383-01A-11D-2129-08 chr19:51506323 C>T did not map to a codon.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:187539226 G>C maps to ENST00000260147 S2841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:187539226 G>C maps to ENST00000260147 S2841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:187629183 G>A maps to ENST00000260147 Q600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7386-01A-11D-2012-08 chr4:187629183 G>A maps to ENST00000260147 Q600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr21:10996074 C>G did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr21:10996074 C>G did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:73919738 C>G did not map to a codon.
Sequencing variant TCGA-CR-7388-01A-11D-2012-08 chr6:73919738 C>G did not map to a codon.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr11:8008700 G>A did not map to a codon.
Sequencing variant TCGA-CR-7390-01A-11D-2012-08 chr11:8008700 G>A did not map to a codon.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr12:46285668 C>T maps to NM_152641.2 R1677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7395-01A-11D-2012-08 chr12:46285668 C>T maps to NM_152641.2 R1677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr19:53367281 T>A did not map to a codon.
Sequencing variant TCGA-CR-7399-01A-11D-2012-08 chr19:53367281 T>A did not map to a codon.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr3:150264528 G>A did not map to a codon.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr3:150264528 G>A did not map to a codon.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr8:26238105 G>A did not map to a codon.
Sequencing variant TCGA-CR-7401-01A-11D-2012-08 chr8:26238105 G>A did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr18:10672751 G>C maps to NM_022068.2 A2647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chr18:10672751 G>C maps to NM_022068.2 A2647A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chrX:151896604 C>T did not map to a codon.
Sequencing variant TCGA-CR-7402-01A-11D-2012-08 chrX:151896604 C>T did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr15:64791534 T>G did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr15:64791534 T>G did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr9:130479016 G>C did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr9:130479016 G>C did not map to a codon.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr6:31964315 G>C maps to NM_007293.2 A1205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5432-01A-02D-1683-08 chr6:31964315 G>C maps to NM_007293.2 A1205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr11:82444615 C>A maps to NM_175885.3 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr11:82444615 C>A maps to NM_175885.3 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr12:121735512 G>A did not map to a codon.
Sequencing variant TCGA-CV-5434-01A-01D-1683-08 chr12:121735512 G>A did not map to a codon.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr1:38181549 G>A maps to ENST00000330210 C542C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr1:38181549 G>A maps to ENST00000330210 C542C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr1:43885834 C>T did not map to a codon.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr1:43885834 C>T did not map to a codon.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr17:76464797 G>A maps to ENST00000389840 I2879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5436-01A-01D-1512-08 chr17:76464797 G>A maps to ENST00000389840 I2879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:201193889 C>T maps to NM_001164586.1 L3458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr1:201193889 C>T maps to NM_001164586.1 L3458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr13:42830657 G>C did not map to a codon.
Sequencing variant TCGA-CV-5442-01A-01D-1512-08 chr13:42830657 G>C did not map to a codon.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr17:44408470 C>A maps to NM_014834.4 T1276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr17:44408470 C>A maps to NM_014834.4 T1276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr3:183535850 C>T maps to NM_024871.2 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5444-01A-02D-1512-08 chr3:183535850 C>T maps to NM_024871.2 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr3:160286031 A>G did not map to a codon.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr3:160286031 A>G did not map to a codon.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr9:140173371 C>T maps to NM_017723.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5976-01A-11D-1683-08 chr9:140173371 C>T maps to NM_017723.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chrX:39933795 G>T maps to NM_001123385.1 S268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-5978-01A-11D-1683-08 chrX:39933795 G>T maps to NM_001123385.1 S268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr9:21971027 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6003-01A-11D-1683-08 chr9:21971027 C>T maps to NM_001195132.1 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr1:201185879 G>A maps to NM_001164586.1 E3198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6433-01A-11D-1683-08 chr1:201185879 G>A maps to NM_001164586.1 E3198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:88428384 G>C did not map to a codon.
Sequencing variant TCGA-CV-6441-01A-11D-1683-08 chr10:88428384 G>C did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:90459385 C>T did not map to a codon.
Sequencing variant TCGA-CV-6936-01A-11D-1912-08 chr1:90459385 C>T did not map to a codon.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr22:21134378 C>G maps to NM_000185.3 S260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6937-01A-11D-2012-08 chr22:21134378 C>G maps to NM_000185.3 S260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr20:3644018 G>A maps to NM_145762.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6940-01A-11D-1912-08 chr20:3644018 G>A maps to NM_145762.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6942-01A-21D-2012-08 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr7:99933530 G>T did not map to a codon.
Sequencing variant TCGA-CV-6945-01A-11D-1912-08 chr7:99933530 G>T did not map to a codon.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr20:56285619 C>T did not map to a codon.
Sequencing variant TCGA-CV-6953-01A-11D-1912-08 chr20:56285619 C>T did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr21:10996102 G>C did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr21:10996102 G>C did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr3:48488143 C>G did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr3:48488143 C>G did not map to a codon.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr4:187630410 G>A maps to ENST00000260147 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6955-01A-11D-2012-08 chr4:187630410 G>A maps to ENST00000260147 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr1:248636650 C>T did not map to a codon.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr1:248636650 C>T did not map to a codon.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr19:49497071 C>G did not map to a codon.
Sequencing variant TCGA-CV-6956-01A-21D-2012-08 chr19:49497071 C>G did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:8008838 C>G did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr11:8008838 C>G did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:54893307 G>A did not map to a codon.
Sequencing variant TCGA-CV-6961-01A-21D-1912-08 chr17:54893307 G>A did not map to a codon.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr16:4897140 A>G did not map to a codon.
Sequencing variant TCGA-CV-7097-01A-11D-2012-08 chr16:4897140 A>G did not map to a codon.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr4:187525109 G>A maps to ENST00000260147 Q3527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7099-01A-41D-2012-08 chr4:187525109 G>A maps to ENST00000260147 Q3527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr19:13080345 G>C did not map to a codon.
Sequencing variant TCGA-CV-7102-01A-11D-2012-08 chr19:13080345 G>C did not map to a codon.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr17:7579574 G>A maps to NM_001126112.1 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7104-01A-11D-2012-08 chr17:7579574 G>A maps to NM_001126112.1 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chrX:72797281 C>G maps to NM_001039840.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7177-01A-11D-2012-08 chrX:72797281 C>G maps to NM_001039840.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:13495994 C>A maps to NM_001045480.1 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7235-01A-11D-2012-08 chr1:13495994 C>A maps to NM_001045480.1 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr6:33041401 A>T did not map to a codon.
Sequencing variant TCGA-CV-7242-01A-11D-2012-08 chr6:33041401 A>T did not map to a codon.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:240255039 G>T maps to ENST00000406993 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr1:240255039 G>T maps to ENST00000406993 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:31962427 C>T maps to NM_007293.2 R916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7245-01A-11D-2012-08 chr6:31962427 C>T maps to NM_007293.2 R916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr16:16425563 T>C did not map to a codon.
Sequencing variant TCGA-CV-7247-01A-11D-2012-08 chr16:16425563 T>C did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:148346963 C>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr1:148346963 C>T did not map to a codon.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr10:17865309 G>A maps to NM_002438.2 W100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7248-01A-11D-2012-08 chr10:17865309 G>A maps to NM_002438.2 W100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr11:62439186 C>T did not map to a codon.
Sequencing variant TCGA-CV-7250-01A-11D-2012-08 chr11:62439186 C>T did not map to a codon.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr1:201196110 G>T maps to NM_001164586.1 E3630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7253-01A-11D-2012-08 chr1:201196110 G>T maps to NM_001164586.1 E3630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr19:571493 G>A did not map to a codon.
Sequencing variant TCGA-CV-7254-01A-11D-2012-08 chr19:571493 G>A did not map to a codon.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr4:70513427 A>G did not map to a codon.
Sequencing variant TCGA-CV-7261-01A-11D-2012-08 chr4:70513427 A>G did not map to a codon.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr11:5757738 G>T did not map to a codon.
Sequencing variant TCGA-CV-7263-01A-11D-2012-08 chr11:5757738 G>T did not map to a codon.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr18:47340564 C>T did not map to a codon.
Sequencing variant TCGA-CV-7413-01A-11D-2078-08 chr18:47340564 C>T did not map to a codon.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr12:247431 G>A did not map to a codon.
Sequencing variant TCGA-CV-7416-01A-11D-2078-08 chr12:247431 G>A did not map to a codon.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:53367248 G>A did not map to a codon.
Sequencing variant TCGA-CV-7424-01A-11D-2078-08 chr19:53367248 G>A did not map to a codon.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr1:115078684 G>C did not map to a codon.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr1:115078684 G>C did not map to a codon.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:93856568 A>C maps to ENST00000513200 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CV-7432-01A-11D-2129-08 chr5:93856568 A>C maps to ENST00000513200 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr6:31994871 C>G maps to NM_001002029.3 L855L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CX-7085-01A-21D-2012-08 chr6:31994871 C>G maps to NM_001002029.3 L855L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:206945858 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr1:206945858 C>T did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:100567227 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr12:100567227 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:64791534 T>G did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr15:64791534 T>G did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:2966430 G>A maps to ENST00000333466 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr17:2966430 G>A maps to ENST00000333466 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:39735637 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr19:39735637 G>A did not map to a codon.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:20685401 G>A maps to NM_001163941.1 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chr7:20685401 G>A maps to NM_001163941.1 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:1314913 C>G maps to ENST00000381567 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6516-01A-11D-1870-08 chrX:1314913 C>G maps to ENST00000381567 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr16:56670368 C>T did not map to a codon.
Sequencing variant TCGA-D6-6824-01A-11D-1912-08 chr16:56670368 C>T did not map to a codon.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr9:21239988 G>A did not map to a codon.
Sequencing variant TCGA-D6-6826-01A-11D-1912-08 chr9:21239988 G>A did not map to a codon.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr15:64982655 G>A maps to ENST00000403937 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr15:64982655 G>A maps to ENST00000403937 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr16:15029130 G>A did not map to a codon.
Sequencing variant TCGA-DQ-5624-01A-01D-1870-08 chr16:15029130 G>A did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr8:144241657 C>T did not map to a codon.
Sequencing variant TCGA-DQ-5629-01A-01D-1870-08 chr8:144241657 C>T did not map to a codon.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr13:42830544 A>G did not map to a codon.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chr13:42830544 A>G did not map to a codon.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chrX:151896273 G>A did not map to a codon.
Sequencing variant TCGA-DQ-5631-01A-01D-1870-08 chrX:151896273 G>A did not map to a codon.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr8:33371003 G>T did not map to a codon.
Sequencing variant TCGA-DQ-7592-01A-11D-2078-08 chr8:33371003 G>T did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr6:168227284 C>T did not map to a codon.
Sequencing variant TCGA-DQ-7595-01A-11D-2229-08 chr6:168227284 C>T did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:56287637 C>G did not map to a codon.
Sequencing variant TCGA-HL-7533-01A-11D-2229-08 chr10:56287637 C>G did not map to a codon.
